<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dcterms="http://purl.org/dc/terms/">
<rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1318">
    <dcterms:title><![CDATA[Volumen 17 Número 4]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:publisher><![CDATA[Juan José Mezzadri]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1317">
    <dcterms:title><![CDATA[TRABAJOS PRESENTADOS A PREMIO]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Trabajos Premiados]]></dcterms:description>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1316">
    <dcterms:title><![CDATA[Epidemiología e impacto socieconóico de la migraña]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Actualización]]></dcterms:description>
    <dcterms:abstract><![CDATA[Los estudios epidemiológicos para establecer la prevalencia e incidencia de la migraña, son relativamente recientes, ya que hasta 1988, en que la &quot;International Headache Society&quot; estableció definiciones y pautas diagnósticas que fueron aceptadas y utilizadas en todo el mundo, no había parámetros para hacer diagnósticos válidos y equivalentes en lo que respecta a esta dolencia. Los autores analizan en este artículo las comunicaciones más representativas efectuadas en países que poseen una organización útil para efectuar encuestas como son Dinamarca, Suecia, Estados Unidos de Norte América, Holanda, etc. Desafortunadamente, no se ha podido realizar una encuesta epidemiológica valedera en nuestro país ya que los intentos efectuados hasta ahora, no alcanzaron un muestreo representativo y por consiguiente debemos extrapolar información de otros ámbitos para arriesgar algunas pautas a ser aplicadas localmente y así podríamos aventuramos a pensar que en Argentina habría 3.960.000 personas que sufren migrañas (el 1 % del total de la población) y que de ellas, posiblemente 2.500.000 personas sufrirían severas crisis con el consiguiente impacto en la actividad individual y comunitaria. En general, se acepta que la prevalencia por vida, de la migraña, es del 15 al 18 % de las mujeres y el 6 % de los hombres. También se ha establecido que la edad de más afectación es entre los 35 a 40 años y estas cifras ya van configurando el impacto socioeconómico de esta dolencia que al invalidar de 1 a4 días por mes a una población en plena capacidad productiva, provoca un severo deterioro personal y social que podría representarse en cifras como han intentado algunos investigadores cuyas conclusiones son mencionadas en este artículo. Es muy útil, al estudiar el impacto de la migraña, tener en cuenta parámetros como el ausentismo, la pérdida de productividad, la alteración en la calidad de vida y el consumo del sistema médico. Los autores concluyen este artículo enfatizando que tanto la migraña, como los otros tipos de cefaleas, tienen una expresión importante en el individuo y en la sociedad y en nuestro medio no está debidamente enfocada esta dolencia, de tal modo que estamos ante una situación más en que todo está aún por hacerse.]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Héctor A. Zavala ]]></dcterms:creator>
    <dcterms:creator><![CDATA[Bibiana B. Saravia]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[Headache Classification Committee of the International Headache Society. Classification and diagnotic criteria for headache disorders, cranial neuralgias and facial pain. Cephalalgia 1988; 8: 19-28.<br />
<br />
Rasmussen BK, Jensen R, Schroll M, Olesen J. Epidemiology of headache in a general population — a prevalence study. J Clin Epidemtol 1991; 44: 1147-57.<br />
<br />
Rasmussen BK. Epidemiology of headache. Cephalalgia 1995; 15: 45-68.<br />
<br />
Rasmussen BK. Epidemiology of Headache. Ce phalalgia 2001; 21: 774-77.<br />
<br />
Lampl C, Buzath A, Baumhackl U, Klingler D. Oneyear prevalence of migraine in Austria: a nationwide survey. Cephalalgia 2003; 23: 280-6.<br />
<br />
Couturier EGM, Bomhof MAM, Neven AK, van Duijn NP. Menstrual migraine in a representative Dutch population sample: prevalence, disability and treatment. Cephalalgia 2003; 23: 302-8.<br />
<br />
Dahltif C,Linde M. One-year prevalence of migraine in Sweden: a population-based study in adults. Cephalalgia 2001; 21: 664-71.<br />
<br />
8. Rasmussen B, Jensen R and Olesen J. A population based analysis of the diagnostic criteria of the International Headache Society. Cephalalgia 1991; 11: 129.<br />
<br />
Schwartz BS, Stewart WF, Simon D et alt. Epidemiology of tension-type headache. JAMA 1998; 279: 381-3.<br />
<br />
Lavados P and Tenhamm E. Epidemiology of tension-type headache in Santiago, Chile a prevalence study. Cephalalgia 1998; 18: 552-8.<br />
<br />
Scher AL, Stewart WF, Liberman J, Lipton RB. Prevalence of frequent headache in a population sample. Headache 1998; 38: 497-506.<br />
<br />
McHorney C, Ware J, Raczek A.E. The MOS 36- item short form health survey (SF-36): II. Psycho­metric and clinical test of validity in measuring physical and mental health constructs. Med. Care 1993; 31: 247-63.<br />
<br />
Hu X, Markson L, Lipton RB et al. Disability and economic costs of migraine in tha United States: A population based approach. Arch. Inter. Med. 1999; 159: 813-8.]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1315">
    <dcterms:title><![CDATA[Subluxación cervical espondiloartrósica]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Trabajos Breves]]></dcterms:description>
    <dcterms:abstract><![CDATA[Objective: To analyze the biomechanical and anatomical factors and the surgical treatment and outcome in cervical degenerative spondylolisthesis.<br />
Method: Between 1978 and 2003, 223 patients underwent surgery for cervical spondylotic myelopathy. 41 patients presented with degenerative subaxial subluxation. According to the Nurick scale, 26 were grade 2, 14 were grade 3 and 1 was grade 4. Those with degenerative subluxation were older compared to those who liad only spondylotic myelopathy (63 vs. 13 years). Theformer also corresponded to higher grades of the Nurick scale. All patients underwent static and dynamic plain radiographs, and MRI. We found 29 subluxations of one level, 11 patients wíth affection of two levels and 1 with three levels. 33 patients liad unstable subluxations. The most commonly affected levels were C3-C4 and C4-05. In all the cases, an anterior approach with autogenous bone graft and locking plate was performed.<br />
Results: After surgical treatment, 21 grade 2 patients improved one grade, while 5 improved two grades; 9 grade 3 patients improved one grade and 1 two grades; the grade 4 patient improved one grade.<br />
Conclusion: Cervical degenerative subluxation is seen in older patients, usually associated with severe myelopathy and spondylotic changes. The cervical instability is more common in the C3-C4 and C4-05 segments. In oil the cases of our group there was a loss of cervical lordosis or kyphosis with ankylosis of the lower cervical spine. The anterior approach with autogenous bone graft and locking Mate, allowed spinal cord decompression and cervical fusion.]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Jorge Shilton]]></dcterms:creator>
    <dcterms:creator><![CDATA[Nilda Ester Goldenberg]]></dcterms:creator>
    <dcterms:creator><![CDATA[ José Carlos Morales]]></dcterms:creator>
    <dcterms:creator><![CDATA[Alberto Zilio]]></dcterms:creator>
    <dcterms:creator><![CDATA[Lucrecia Valdez]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[Perlman R, Hawes LE: Cervical spondylolisthesis. J Bone Joint Surg 1951; 33A: 1012-3.<br />
<br />
Pellengahr C, Pfahler M, Kuhr et al: Influence of facet joint angles and asymmetric disc collapse on degenerative olisthesis of the cervical spine. Orthopedics 2000; 23: 697-701<br />
<br />
Boulos AS, Lovely TJ: Degenerative cervical spondylolisthesis: Diagnosis and management in five cases. J Spinal Disord 1996; 9: 241-5.]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1314">
    <dcterms:title><![CDATA[Tratamiento endoscopico de los quistes aracnoideos supratentoriales de linea media]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Nota Técnica]]></dcterms:description>
    <dcterms:abstract><![CDATA[Objetivo. El propósito de esta presentación es analizar el rol de la neuroendoscopia en el tratamiento de los quistes aracnoideos supratentoriales de línea media.<br />
Descripción. Se han utilizado neuroendoscopios rígidos Wolf ®, Storz ® o Aesculap ® según los casos. El instrumental auxiliar utilizado ha consistido en pinza de biopsia, tijera, electrodo mono y/o bipolar y catéterbalón tipo Fogarty 3 F. El equipamiento complementario lo constituyen una videocámara de alta resolución, una fuente de luz fría y un monitor de alta definición, de acuerdo a su disponibilidad. Las imágenes han sido registradas por medio de un capturador fotográfico digital y de un videograbador. <br />
Resultados. La técnica neuroendoscópica ha permitido el tratamiento quirúrgico de los quistes aracnoideos supratentoriales de línea media en forma mínimamente invasiva comunicando estas lesiones con las cisternas basales y/o el sistema ventricular. Conclusión. La vecindad de estas lesiones con el sistema ventricular resulta ideal para su fenestración endoscópica y comunicación con las vías de circulación del líquido cefalorraquídeo.]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Edgardo Schijman]]></dcterms:creator>
    <dcterms:creator><![CDATA[Guillermo Fernández Molina]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[Hinojosa J, Esparza J, Munoz MJ, Valencia J. Endoscopic treatment of suprasellar arachnoid cysts. Neurocirugía (Astur) 2001; 12: 482-8.<br />
<br />
Ciricillo SF, Cogen PH, Harsh GR, Edwards MSB. Intracranial arachnoid cysts in children. A comparison of the effects of fenestration and shunting. J Neurosurg 1991; 74; 230-5<br />
<br />
Raffel C, McComb JG. To shunt or to fenestrate: which is the best surgical treatment for arachnoid cysts in pediatric patients ? Neurosurgery 1988; 23: 338-2<br />
<br />
Decq P, Brugieres P, Le Guerinel C, Djindjian M, Keravel Y, Nguyen J-P. Percutaneous endoscopic treatment of suprasellar arachnoid cysts: ventriculocystostomy or ventriculocystocystemostony? J Neurosurg 1996; 84: 696-1<br />
<br />
Miyajima M, Arai H, Okuda O, Hishii M, Nakanishi H, Sato K. Possible origin of suprasellar arachnoid cysts: neuroimaging and neurosurgical observations in nine cases. J Neurosurg 2000; 93: 62-7.<br />
<br />
Oberbauer RW, Haase L, Pucher R. Arachnoidcysts in children: a European co-operative study. Child&#039;s Nerv Syst 1992; 8: 281-6<br />
<br />
Choi J-U, Kim D-S. Pathogenesis of arachnoid cysts: congenital or traumatic? Pediatr Neurosurg 1998; 29: 260-6<br />
<br />
Pierre-Kahn A, Capelle L, Bruner R, Sainte-Rose C, Renier D, Rappaport R, Hirsch J-F. Presentation and management of suprasellar arachnoid cysts. Review of 20 cases. J Neurosurg 1990; 73: 355-9<br />
<br />
Buxton N, Vloeberghs M, Punt J. Flexible neuroendoscopic treatment of suprasellar arachnoid cysts. Br J Neurosurg 1999; 13: 316-8<br />
<br />
Choi J-U, Kim D-S, Huh R. Endoscopic approach to arachnoid cyst. Child&#039;s Nerv Syst 1999; 15: 285-1<br />
<br />
Kirollos RW, Javadpour M, May P, Mallucci C. Endoscopic treatment of suprasellar and third ventricle-related arachnoid cysts. Child&#039;s Nerv Syst 2001; 17: 713-8]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1313">
    <dcterms:title><![CDATA[Hemorragia subaracnoidea por disección aneurismática de la arteria vertebral intradural. Presentación de 2 casos y análisis de la enfermedad]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Trabajos Breves]]></dcterms:description>
    <dcterms:abstract><![CDATA[Objective: To describe 2 cases of vertebral artery dissecting aneurysms.<br />
Description: We present 2 cases with vertebral artery dissecting aneurysms. The first patient liad spontaneous occlusion of the lesion, the second showed a persistent fusiform dilatation of the artery.<br />
Intervention: Early treatment is recommended. The patient who showed spentaneous cure of the dissection was followed with angiography. The second case was occluded with coil.<br />
Conclusion: The endovascular occlusion of these lesion is an efflcacious and safer procedure than surgical clipping.<br />
]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Flavio Requejo]]></dcterms:creator>
    <dcterms:creator><![CDATA[Horacio Fontana]]></dcterms:creator>
    <dcterms:creator><![CDATA[Héctor Belziti]]></dcterms:creator>
    <dcterms:creator><![CDATA[Mario Recchia]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[Anxionnat R, Ferreira de Melo Neto J, Bracard S, Lacour JC, Pinelli C, Civit T et al: Treatment of hemorrhagic intracranial dissections. Neurosurgery 2003; 53: 289-301.<br />
<br />
Cecinano AR, Lemme-Plaghos LA, Garbugino SL, Schónholz CJ, Mendaro EE: Pseudoaneurismas por disección de la arteria vertebral intradural: tratamiento endovascular. Rey Argent Neuroc 1995; 9: 102-6.<br />
<br />
Kitanaka C, Tanaki JL, Kuwahara M, Teraoka A, Sasaki T, Takakura K: Nonsurgical treatment of unruptured intracranial vertebral artery dissection with serial follow-up angiography. J Neurosurg1994; 80: 667-74.<br />
<br />
Lylyk P, Ceratto R, Cohen JE Ferrario A, Miranda C: Combined endovascular treatment of dissecting vertebral artery aneurysms by using stents and coils. J Neurosurg 2001; 94: 427-32.<br />
<br />
Pozzati E, Padovani R, Fabrizi A, Sabattini L, Gaist G: Benign arterial dissections of the posterior circulation. J Neurosurg 1991; 75: 69-72.<br />
<br />
Yonas H, Agamanolis D, Takaoka Y, White RJ: Dissecting intracranial aneurysms. Surg Neurol 1977; 8: 407-15.]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1312">
    <dcterms:title><![CDATA[Cisticercosis espinal: a propósito de un caso]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Serie de Casos]]></dcterms:description>
    <dcterms:abstract><![CDATA[Objetivo. Comunicar el caso de una paciente de 53 años, oriunda de zona endémica de América Latina, con signos de compresión medular dorsal secundarios a una cisticercosis espinal .<br />
Descripción. Paciente de sexo femenino, cuadro progresivo de compresión medular dorsal, con antecedentes de neurocisticercosis. Las neuroirnágenes mostraron una lesión intradural-extramedular D5-D6.<br />
Intervención. Se abordó quirúrgicamente en posición lateral, verificándose aracnoiditis reaccional y quiste de cisticerco que fue resecado, completándose el tratamiento con Albendazol oral, con regresión de la paraparesia severa preoperatoria y satisfactorio control imagenológico.<br />
Conclusión. La forma espinal es infrecuente en el curso de la neurocisticercosis. La terapéutica implementada en nuestro caso fue concordante con los pocos casos descriptos en la literatura mundial<br />
]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Marcelo Platas]]></dcterms:creator>
    <dcterms:creator><![CDATA[Diego Riva]]></dcterms:creator>
    <dcterms:creator><![CDATA[Alee Castro]]></dcterms:creator>
    <dcterms:creator><![CDATA[Jorge Marche]]></dcterms:creator>
    <dcterms:creator><![CDATA[Dario Savini]]></dcterms:creator>
    <dcterms:creator><![CDATA[Aquiles Uccelli]]></dcterms:creator>
    <dcterms:creator><![CDATA[Daniel Aguayo]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[Mandell D, Bennett&#039;s: .Principles and Practice of Infectious Diseases; Parte II; Sección H; Capítulo 72; Churchill Livingstone; 5ta edición, 2000.<br />
<br />
Corral I, Quereda C, Moreno A, López Vélez R, Martínez San Millan J, Guerrero A, et al. Intramedullary cysticercosis; Spine 1996; 21: 2284-7<br />
<br />
Robertson H, Watson J. Neurocysticercosis with ceivical meningeal invovement; AJR 1978; 171: 877-88.<br />
<br />
Leite C, Jinkins R, Escobar B, Magalhaes A, Gomes G, Dib G, et al. MRI imaging of spinal cysticercosis; AJR 1997; 169: 1713-7.<br />
<br />
Corr P, Royston D, Naidoo HT. The role of imaging in diagnosis of unusual spinal infection; Int J Neuroradiol 1999; 5: 200-1.]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1311">
    <dcterms:title><![CDATA[Nuevo retractor para microdiscectomía]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Nota Técnica]]></dcterms:description>
    <dcterms:abstract><![CDATA[Objetivo. Describir un nuevo restractor espinal.<br />
Descripción. Una valva del retractor de Taylor se une al retractor de Yasargil para sostener y separar los músculos paravertebrales.<br />
Conclusión. Esta variante de retractor expone el campo quirúrgico sin dañar las estructuras de la línea media.]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Heraldo R. Parés]]></dcterms:creator>
    <dcterms:creator><![CDATA[Gabriel A. Pauletti]]></dcterms:creator>
    <dcterms:creator><![CDATA[Iván Aznar]]></dcterms:creator>
    <dcterms:creator><![CDATA[Francisco R. Papalini]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[Mixter WJ, Barr Js: Rupture of the intervertebral disc disease with involvement of the spinal canal. N Engl J Med 1934; 211: 210-5.<br />
<br />
Caspar W: A new surgical procedure for lumbar disc herniation causing less tissue damage through a microsurgical approach. Adv Neurosurg 1977; 4: 74-7.<br />
<br />
Yasargil MG: Microsurgical operation of the herniated lumbar disc. Adv Neurosurg 1977; 4: 81-91.<br />
<br />
Williams RW: Microlumbar discectomy: A conservative surgical approach to the virgin herniated lumbar disc. Spine 1978; 3: 175-82.<br />
<br />
Bell WO, Lavyne MH: Retractor for lumbar microdiscectomy: Technical note. Neurosurgery 1984; 14: 69-70.<br />
<br />
Goald HJ: Microlumbar discectomy: Follow-up of 477 patients. J Microsurg 1980; 2: 95-100.<br />
<br />
Wilson DH, Harbaugh R: Microsurgical and standard removal of the protruded lumbar disc: A comparative study. Neurosurgery 1981; 8: 422-27.<br />
<br />
Wilson DH, Kenning J: Microsurgical lumbar discectomy: Preliminary report of 83 consecutive cases. Neurosurgery 1979; 4: 137-40.<br />
<br />
Taylor GM: A simple retractor for spinal surgery. J Bone Joint Surg 1946; 28A: 183-4.]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1310">
    <dcterms:title><![CDATA[Meningiomas quisticos: presentacion de 3 casos]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Trabajos Breves]]></dcterms:description>
    <dcterms:abstract><![CDATA[Objective: To describe 3 cases of intracranial cystic meningioma.<br />
Description: Case 1 (male, 24 years old), with headache, vomits, right homonymous hemianopsia and conductal disorder, in the last 2 months. MRI: left parieto-occipital cystic tumor. Case 2: (male, 56 years old) with left brachiocrural palsy, in the past year. CT scan: left parietal cystic tumor. Case 3: (female, 56 years old) with generalized siezure, in the last month. 114 R left parietal cystic tumor. In the three cases, the suspected diagnose was glioma.<br />
Intervention: In the 3 cases a craniotomy was performed, with total (cases 2 and 3) or partial resection of the tumor (case 1). The cysts were intratumoral (case 2) and extratumoral (cases 1 and 3). Pathology informed meningioma. The outcome was favorable, with no complications.<br />
Conclusion: It is very difficult to make a diagnosis of cystic meningioma before surgery procedure and pathological analysis. During surgery they behave as solid. meningiomas. Key words: craniotomy, cystic meningioma, cystic tumor.]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Mariano Pallavicini]]></dcterms:creator>
    <dcterms:creator><![CDATA[Juan C. Dobarro]]></dcterms:creator>
    <dcterms:creator><![CDATA[Santiago González Abbati]]></dcterms:creator>
    <dcterms:creator><![CDATA[ Jorge Holguín]]></dcterms:creator>
    <dcterms:creator><![CDATA[ Pablo Jalón]]></dcterms:creator>
    <dcterms:creator><![CDATA[ Alvaro Campero]]></dcterms:creator>
    <dcterms:creator><![CDATA[ Juan J. Mezzadri]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[McDermott M W., Wilson B C. Meningiomas. En: Neurological Surgery. Youman J, editor, Philadelphia: Saunders, 1996; pp. 2782-825.<br />
<br />
El-Filki M., El-Henawy Y, Abdel-Arman N. Cystic Meningioma. Acta Neurochir (Wien) 1996;138: 811-7.<br />
<br />
Chen C Th, Zee Ch, Miller A C, Weiss H M, Tang G, Chin L, et al. Magnetic resonance imaging and pathological correlates of meningioma. Neurosurgery 1992; 31: 1015-9.<br />
<br />
Suzuki Y., Sugimoto T., Shibuya M., Sugita K., Patel J S. Meningioma: Correlation between MRI characteristics and operative findings including consistency. Acta Neurochir (Wien) 1994; 129: 29-46.<br />
<br />
<br />
<br />
]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1309">
    <dcterms:title><![CDATA[Artefactos metálicos en resonancia magnética postdiscectomía cervical anterior con injerto sin instrumentación]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Serie de Casos]]></dcterms:description>
    <dcterms:abstract><![CDATA[Objetivo. Describir y analizar las imágenes por resonancia magnética (IRM) de artefactos postdiscectomía cervical anterior con injerto sin instrumentación.<br />
Descripción. Se presentan 2 casos de sexo femenino, 47 y 40 años, con una mielopatía cervical progresiva, causada por una hernia dura y blanda a nivel C5-6 respectivamente, diagnosticada con IRM. Se efectuó una discectomía anterior con autoinjerto tricortical. Evolucionaron favorablemente de su mielopatía, persistiendo dolores cervicales moderados en el segundo caso.<br />
Intervención. Los controles postoperatorios con IRM mostraron en los distintos cortes, imágenes de intensidad mixta, contornos irregulares y bordes difusos, que simulaban patología residual. La radiografia simple (Rx) y la tomografia axial computada (TAC) postoperatorias fueron normales. Lafalta de coincidencia clínica-IRM e IRM-Rx-TAC hizo suponer que dichas imágenes eran artefactos, probablemente metálicos.<br />
Conclusión: Las imágenes postoperatorias de intensidad mixta que ocupan el canal a nivel del disco operado pueden ser artefactos; la Rx y TAC suelen aclarar el diagnóstico. ]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Juan José Mezzadri]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[Bohlman HH. Cervical spine: degenerative disease. En: Boden SD &amp; Bohlman HH, editors. The Failed Spine. Philadelphia: Lippincott Williams &amp; Wilkins; 2003. pp. 30-47.<br />
<br />
Salazar JL, Misra MM, Bloom D, Dobben G. MRI artifacts following anterior cervical diskectomy. Surg Neurol 1997; 48: 23-9.<br />
<br />
Arunkumar MJ, Rajshenkhar V. Artifacts in magnetic resonance images following anterior cervical discectomy and fusion: report of two cases. British J Neurosurg 1998; 12: 553-5.<br />
<br />
Ruggieri PM. A practical approach to magnetic resonance physics in spinal imaging. En: Modic MT, Masaryk TJ &amp; Ross JS, editors. Magnetic Resonance Imaging of the Spine. St. Louis: Mosby; 1994. pp.1-36.<br />
<br />
Toro VE, Goodrich A, Lundy DW, Meeks L, Figueroa RE, Binet EF. MR artifacts after anterior cervical diskectomy and fusión: a cadaver study. J Comput Assist Tomogr 1993; 17: 696-9.<br />
<br />
Tartaglino LM, Flanders AE, Vinitski S, Friedman DP. Metallic artifacts on MR images of the postoperative spine: reduction with fast spin-echo techniques. Radiology 1994; 190: 565-9.]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1308">
    <dcterms:title><![CDATA[Granuloma eosinófilo solitario de vértice de órbita y senos paranasales en un adulto: comunicación de un caso y revisión de la literatura]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Trabajos Breves]]></dcterms:description>
    <dcterms:abstract><![CDATA[Objective: To report a rare localization of Langerhans&#039; cell histiocytosis,and to define its differential diagnosis and therapeutic options.<br />
Description: A32 year-old mole with decreasing visual acuity, headache and epistaxis. MRI: parasellar lytic lesion extending to nasal cavities. Transnasal biopsy: proltferation of S100 positive cells and eosinophilic granulocytes.<br />
Intervention: Radiation therapy was followed by remission.<br />
Conclusion: Langerhans&#039; cell histiocytosis can present as a unifocal (eosinophilic granuloma) or multifocal disorder. Usually affects children. The skull base is rarely affected. Surgery with or without radiotherapy is the treatment of choice for solitary accessible lesions. Isolated radiotherapy and intralesional steroids are valid options. Systemic disease requires chemotherapy.]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Patricia Maggiora]]></dcterms:creator>
    <dcterms:creator><![CDATA[ Marcelo Amante ]]></dcterms:creator>
    <dcterms:creator><![CDATA[Alberto Gidekel]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Kaufman A, Bukberg PR, Werlin S, Young IS. Multifocal eosinophilic granuloma(&quot;Hand-SchullerChristian Disease&quot;). Report illustrating H-S-C chronicity and diagnostic challenge. Am J Med 1976; 60: 541-8<br />
<br />
Komp D. Langerhans cell (eosinophilic) granulomatosis. En: Bennet JC, Plum F, editores. Cecil Textbook of Medicine. 20th ed. Philadelphia: W.B. Saunders Company; 1996. p. 955-6.<br />
<br />
Sampson JH, Rossitch E Jr, Young JN, Lane KN, Friedman AH. Solitary eosinophilic granuloma invading the clivus of an adult: case report. Neurosurgery 1992; 31:755-7.<br />
<br />
Brisman JL, Feldstein NA, Tarbell NJ, Cohen D, Cargan AL, Haddad J Jr et al. Eosinophilic granuloma of the clivus: case report, follow up of two previously reported cases, and review of the literature on cranial base eosinophilic granuloma. Neurosurgery 1997; 41: 273-8.<br />
<br />
Lederman CR, Lederman ME. Unifocal Langerhans cell histiocytocis in the clivus of a child with abducens palsy and diplopia. J AAPOS 1998; 2: 378-9.<br />
<br />
Wirtschafter JD, Nesbit M, Anderson P, McClain K. Intralesional methylprednisolone for Langerhans&#039; cell histiocitosis of the orbit and cranium. J Pediatr Ophthalmol Strabismus 1987; 24: 194-7.]]></dcterms:dateAccepted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1307">
    <dcterms:title><![CDATA[In memoriam]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Obituarios]]></dcterms:description>
    <dcterms:creator><![CDATA[Dr. Guido Gabriel Gioino ]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1306">
    <dcterms:title><![CDATA[Hematoma subdural subagudo y crónico: tratamiento quirúrgico en 176 pacientes. Nuestra experiencia.]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Trabajos Breves]]></dcterms:description>
    <dcterms:abstract><![CDATA[Objective. To describe our surgical experience in subacute and chronic subdural hematomas.<br />
Method. 176 patients with subacute or chronic subdural hematomas were operated between June 1998 and May 2003. Hospital records were used to ascertain data. We did a comparative analysis of the different types of surgical procedures performed. <br />
Results. The surgical procedure commonly performed was a burrhole craniostomy with subdural closed-system drainage (66%). This procedure was associated with a low rate of complications and reoperations, in comparison with the burr hole craniostomy or the craniostomy without subdural closed-system drainge. Global recurrence rate was 13% and 20.4% of the cases required reoperation. Clinical improvement rate was 72.3%. <br />
Conclusion. In our cases, burr hole craniostomy with closed-system drainge was the method of choice for the initial treatment in subacute and chronic subdural hematomas. Craniotomy should be reserved for those cases of recurrence or residual hematoma. Key words: chronic subdural hematoma, subacute subdural hematoma, subdural drainage]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Santiago González Abbati]]></dcterms:creator>
    <dcterms:creator><![CDATA[Jorge Holguín]]></dcterms:creator>
    <dcterms:creator><![CDATA[Mariano Pallavicini]]></dcterms:creator>
    <dcterms:creator><![CDATA[Juan C. Dobarro]]></dcterms:creator>
    <dcterms:creator><![CDATA[Pablo Jalón]]></dcterms:creator>
    <dcterms:creator><![CDATA[Alvaro Campero]]></dcterms:creator>
    <dcterms:creator><![CDATA[Patricia Ciavarelli]]></dcterms:creator>
    <dcterms:creator><![CDATA[Ricardo Fernández]]></dcterms:creator>
    <dcterms:creator><![CDATA[Antonio Carrizo]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[Sambasivan M: An ovenview of chronic subdural hematoma: experience with 2300 cases. Surg Neurol 1997; 47: 418-22.<br />
<br />
Ernestus R, Beldzinski P, Lanfermann H, Klug N: Chronic subdural hematoma: surgical treatment and outcome in 104 patients. Surg Neurol 1997; 48: 220-5.<br />
<br />
Tabaddor K, Shulman K: Definitive treatment of chronic subdural hematoma by twist-drill craniostomy and closed-system drainage. J Neurosurg 1977; 46: 220-6.<br />
<br />
Voelker J, Sambasivan M: The role of craniotomy and trephination in the treatment of chronic subdural hematoma. Neurosurg Clin N Am 2000; 11: 535-40.<br />
<br />
Markwalder T, Steinsiepe K, Rohner M, Reichenbach W, Markwalder H: The course of chronic subdural hematomas alter burr-hole craniostomy and closed-system drainage. J Neurosurg 1981; 55: 390-6.]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1305">
    <dcterms:title><![CDATA[Disecciones carotídeas espontáneas complicadas: a propósito de dos casos tratados por vía endovascular]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Trabajos Breves]]></dcterms:description>
    <dcterms:abstract><![CDATA[Objective: To report 2 cases of spontaneous carotid dissection (SCD) that presented a pseudoaneurysm as a complication.<br />
Description: We report a case of a 47 year old patient with headache and Horner syndrome. The digital angiography (DA) showed a SCD. That was followed by a pseudoaneurysm. A 46 year old patient presented with a right amaurosis fugax and left hemiparesis. A SCD was diagnosed by magnetic resonance angiography. It presented with a pseudoaneurysm.<br />
Intervention: Both pseudoaneurysm were treated with stents.<br />
Conclusion: DA is the method of choicefor the diagnosis and evolutive dynamic control of SCD. Stents are useful pseudoaneurysm resolution.]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Maximiliano Genesio]]></dcterms:creator>
    <dcterms:creator><![CDATA[Walter Casagrande]]></dcterms:creator>
    <dcterms:creator><![CDATA[Silvia Garbugino]]></dcterms:creator>
    <dcterms:creator><![CDATA[Marcelo Notrika]]></dcterms:creator>
    <dcterms:creator><![CDATA[Luis LemmePlaghos]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[Anson J, Crowell RM. Cervicocranial arterial dissection. Neurosurgery 1991; 28: 89-96.<br />
<br />
Biller J, Hingtgen WL, Adams HP, Smocker WR, Godersky JC, Toffol GJ. Cervicocephalic arterial dissections: A ten-year experience. Arch Neurol 1986; 43:1234-8.<br />
<br />
Friedman WA, Day AL, Quisling RG, Sypert GW, Rhoton AL Jr. Cervical carotid dissecting Aneurysms. Neurosurgery 1980; 7: 207-214.<br />
<br />
Kremer C, Mosso M, Georgiadis D, Stockli E, Benninger D, Arnold M et al: Carotid dissection whit permanent and transient occlusion or severe stenosis: Long-term outcome. Neurology 2003; 60: 271-275.<br />
<br />
Malek AM, Higashida RT, Phatouros CC, Malek AM, Lempert TE, Dowd CF et al: Endovascular management of extracranial carotid artery dissection achieved using stent angioplasty. AJNR 2000; 21: 1280-92.<br />
<br />
Pozzati E, Gaist G, Poppi M: Resolution of occlusion in spontaneously dissected carotid arteries: Report of two cases. J Neurosurg 1982; 56: 857-60.]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1304">
    <dcterms:title><![CDATA[Glioblastoma multiforme de fosa posterior. Presentación de un caso]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Trabajos Breves]]></dcterms:description>
    <dcterms:abstract><![CDATA[Objective: to report a case of glioblastoma multiforme (GBM) of the posterior fossa. <br />
Description: mate, 53 years old, with a clinical presentation of dizziness and diplopia. MRI: posterior fossa tumor in the left cerebellar hemisphere, with an extension to the peduncle, brain stem and cerebellopontine angle.<br />
Intervention: a subtotal ressection was performed through a suboccipital craniotomy. Pathology informed GBM. After surgery the patient completed the treatment with radiotherapy (60 Gy). The outcome was favorable.<br />
Conclusion: the preoperative diagnosis of a posterior fossa GBM is difficult because its a extremely rare localization, nevertheless it must be suspected.<br />
Key words: high grade glioma, glioblastoma multiforme, radiotherapy.]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Juan C. Dobarro]]></dcterms:creator>
    <dcterms:creator><![CDATA[Santiago González Abbati]]></dcterms:creator>
    <dcterms:creator><![CDATA[Jorge Holguín]]></dcterms:creator>
    <dcterms:creator><![CDATA[Mariano Pallavicini]]></dcterms:creator>
    <dcterms:creator><![CDATA[Alvaro Campero]]></dcterms:creator>
    <dcterms:creator><![CDATA[Antonio Carrizo]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[Helseth A, Mark SJ. Neoplasms of the central nervous system in Norway: III. Epidemiological characteristics of intracranial gliomas according to histology. A.P.M.I.S. 1989; 97: 547-55.<br />
<br />
Luccarelli G. Glioblastoma multiforme of cerebellum: Description of three cases. Acta Neurochir (Wien) 1980; 53: 107-16.<br />
<br />
Russell D, Rubinstein L. Pathology ofTumors of the Central Nervous System. 5th ed. Baltimore, Williams &amp; Wilkins, 1989, p. 1012.<br />
<br />
Fiveash J, Spencer S. Role of radiation therapy and radiosurgery in glioblastoma multiforme. Cancer 2003; 9: 222-9.<br />
<br />
Lacroix M, Abi-Said D. A multivariate analysis of 416 patients with glioblastoma multiforme: prognosis, extent of resection, and survival. J Neurosurg 2001; 95: 190-8.<br />
<br />
Afra D, Baron B, Bonadonna G. Chemotherapy in adult high-grade glioma: a systematic review and meta-analysis of individual patient data from 12 randomised trials. Lancet 2002; 359:1011-8.]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1303">
    <dcterms:title><![CDATA[Cisterna ambiens: Anatomía microquirúrgica y abordajes]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Trabajos Breves]]></dcterms:description>
    <dcterms:abstract><![CDATA[Objective: To define the limits of the ambient cistem and to show the different ways to approach that space.<br />
Method: Fourformalin-fixed adults heads were examined using X 6 to X 40 magnification. The vessels were filled with colored silicon.<br />
Results: The ambient cistem is located in both sides of the mesencephalon; it is in relation with the crural cistem in front, the cuadrigeminal cistem behind and the cerebellopontine cistem bellow.The diferent approaches to the ambient cistem are: 1) transchoroidal approach, 2) infraoccipital transtentorial approach and 3) supracerebeIIar transtentoriaI approach.<br />
Conclusion: The transchoroidal, infraoccipital transtentorial and supracerebellar trans­tentorial are options when there are a lesion in the ambient cistern.]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Álvaro Campero]]></dcterms:creator>
    <dcterms:creator><![CDATA[Carolina Martins]]></dcterms:creator>
    <dcterms:creator><![CDATA[Alexandre Yasuda]]></dcterms:creator>
    <dcterms:creator><![CDATA[Santiago González Abbati&#039;]]></dcterms:creator>
    <dcterms:creator><![CDATA[Juan Dobarro]]></dcterms:creator>
    <dcterms:creator><![CDATA[Ricardo Fernandez]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[Yasargil MG. Normal Cisternal Anatomy, en: Yasargil MG editor, Microneurosurgery: Microsurgical Anatomy of the Basal Cisterns and Vessels of the Brain, Diagnostics Studies, General Operative Techniques and Phatological Considerations of the Intracraniál Aneurysms. Stuttgart: Georg Thieme Verlag, 1984, Vol I, pp. 25-52.<br />
<br />
Liliequist B. The subarachnoid cisterns.An anatomic and roentgenologic study. Acta Radiol (supp.) 185:1-108, 1959.<br />
<br />
Liliequist B: The anatomy of the subarachnoid cisterns. Acta Radiol 1956; 46: 61-71.<br />
<br />
Ikeda K, Shoin K, Mohri M, Kijima T, Someya S,<br />
<br />
Yamashita J. Surgical indications and microsurgical anatomy of the transchoroidal fissure approach for lesions in and around the ambient cistern. Neurosurgery 2002; 50: 1114-20.<br />
<br />
Smith KA, Spetzler RF. Supratentorial-infraoccipital approach for posteromedial temporal lobe lesions. J Neurosurg 1995; 82: 940-4.<br />
<br />
Yonekawa Y, Imhof HG, Taub E, Curcic M, Kaku Y, Roth P et al. Supracerebellar transtentorial approach to posterior temporomedial structures. J Neurosurg 2001; 94: 339-45.<br />
<br />
<br />
<br />
]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1302">
    <dcterms:title><![CDATA[Pseudomeningocele postcirugía de columna lumbar comunicación de dos casos]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Serie de Casos]]></dcterms:description>
    <dcterms:abstract><![CDATA[Objetivo. Describir 2 casos de pseudomeningocele lumbar postoperatorio.<br />
Descripción. Reportamos dos casos de pseudomeningocele crónico secundario a cirugía de columna lumbar diagnosticados por TAC/ RNM. La solución de continuidad dural en un caso fue objetivada por mielototomografia y en el otro por RNM con secuencia de dinámica de flujo de LCR.<br />
Intervención. Ambos casos fueron tratados quirúrgicamente con cierre del defecto dural obteniéndose buenos resultados posoperatorios.<br />
Conclusión. La presencia de dolor radicular en el contexto de un pseudomeningocele postquirúrgico es un signo indirecto de atropamiento radicular y herniación de la misma a través del defecto dural y / o aracnoideo lo que debe ser resuelto quirúrgicamente para evitar el déficit neurológico irreversible.]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Mario Amaolo]]></dcterms:creator>
    <dcterms:creator><![CDATA[Sergio Pallini]]></dcterms:creator>
    <dcterms:creator><![CDATA[Vilma Passante]]></dcterms:creator>
    <dcterms:creator><![CDATA[Daniel Desole]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:references><![CDATA[Lee KS, Ardi IM: Postlaminectomy lumbar pseudomeningocele: report of four cases. Neurosurgery 1992; 30: 111-4.<br />
<br />
Hadani M, Findler F, Knoler N, Tadmor R, Sahar A, Shacked I: Entrapped nerve root in pseudomeningocele after laminectomy: report of three cases. Neurosuergery 1986; 19: 405-7.<br />
<br />
Shapiro SA, Scully T: Closed continuous drainage of CSF via a lumbar subarachnoid catheter for treatment or prevention of cranial/spinal cerebrospinal fluid fistula. Neurosurgery 1992; 30: 241-5<br />
<br />
Schumacher HW, Wassman H, Podlinski C: Pseudomeningocele of the lumbar spine. Surg Neurol 1988; 29: 77-8.<br />
<br />
O&#039;Connor D, Maskery N, Griffiths G: Pseudomeningocele nerve root entrapment after lumbar discectomy. Spine 1998; 23: 1501-2.<br />
<br />
Stambough JL, Templin CR, Collins J: Subarachnoid drainage of an established or chronic pseudomeningocele. J Spinal Disorders 2000; 12: 39-41.]]></dcterms:references>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1301">
    <dcterms:title><![CDATA[Finalizamos el año ...]]></dcterms:title>
    <dcterms:description><![CDATA[Editorial]]></dcterms:description>
    <dcterms:creator><![CDATA[Juan Jose Mezzadri<br />
]]></dcterms:creator>
    <dcterms:creator><![CDATA[Luis Lemme-Plaghos]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Luis Augusto Lemme-Plaghos]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2003]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1300">
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1299">
    <dcterms:title><![CDATA[Noticia del Editor de la WFNS<br />
]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Cartas al editor]]></dcterms:description>
    <dcterms:creator><![CDATA[Eduardo A. Karol, MD]]></dcterms:creator>
    <dcterms:publisher><![CDATA[León Turjanski]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2000]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1298">
    <dcterms:title><![CDATA[Abordaje lumbar intermuscular de wiltse en patología no discal]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Artículo Original]]></dcterms:description>
    <dcterms:abstract><![CDATA[Se analizan los resultados obtenidos en tres casos de patología no discal, que comprometían las áreas foraminal y extraforaminal, con el abordaje lumbar intermuscular de Wiltse. El caso 1 (sexo femenino/ 59 años) con antecedentes de linfoma primario de piel, padecía un dolor radicular en L5 causado por un tejido hiperintenso en las IRM ubicado en L5-S1. La biopsiafue inespecífica. El caso 2 (sexofemenino/ 33 años) padecía un dolor radicular L5 causado por una megapófisis transversa en L5 que fue resecada. El caso 3 (sexo femenino/ 23 años) con antecedentes de haber sido operada en la infancia de un tumor congénito, mostraba en las IRM un tejido hiperintenso extenso que invadía el canal a través de varios forámenes entre D12 y L4. La biopsia dio ganglioneuroma. El dolor radicular desapareció en todos los casos. El alta a las 72 horas fue sin complicaciones. Este es un abordaje de bajo riesgo, directo, que se facilita con el empleo de técnicas microquirúrgicas.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[We analyse the results obtained with the Wiltse lumbar intermuscular approach in three cases with non-discal pathology which compromised the foraminal and extraforaminal areas. Case 1 (female/ 59 years) with a history of primary skin lymphoma, sufferedfrom L5 radicular pain caused by an L5-S I hyperintense tissue in MRI. Biopsy was not specific. Case 2 (female/ 33 years) suffered from L5 radicular pain caused by a left megatransverse L5 process which was completely resected. Case 3 (female/ 23 years) with a history of abdominal surgery for a congenital tumour, the MRI showed an hyperintense tissue that invaded extensively de spinal canal through T12-L4 foramina. Biopsy informed ganglioneuroma. After surgery radia llar pain gave up in cases 1 &amp; 2. After 72 hours patients were discharged without complications. This was a safe and dírect approach that was greatly assisted by microsurgical techniques.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Juan José Mezzadri]]></dcterms:creator>
    <dcterms:creator><![CDATA[ Conrado Rivadeneira]]></dcterms:creator>
    <dcterms:creator><![CDATA[Alvaro Campero]]></dcterms:creator>
    <dcterms:creator><![CDATA[Armando Basso]]></dcterms:creator>
    <dcterms:publisher><![CDATA[León Turjanski]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2000]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[Darden BV, Wade F, Alexander R, Wood KE, Rhyne AL, Hicks JR. Far lateral disc herniations treated by microscopic fragment excision. Techniques and results. Spine 20: 1500-1505, 1995.<br />
Geijo R, Matsui H, Kawaguchi Y, Ishihara H, Tsuji H. Serial changes in trunk muscles performance alter posterior lumbar surgery. Spine 24: 1023­1028, 1999.<br />
Hodges SD, Humpreys SC, Eck JC, Covington LA. The surgical treatment of far lateral L3-L4 and L4-L5 disc herniations. A modified technique and outcome analysis of 25 patients. Spine 24: 1243­1246, 1999.<br />
McCulloch JA, Young PH. Foraminal and extraforaminal lumbar disc herniation. En JA McCulloch &amp; PH Young (Eds.), Essentials of Spinal Microsurgery, Lippincott-Raven Publishers, Philadelphia, pp. 383-428, 1998.<br />
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Porchet F, Chollet-Bornand A, de Tribolet N. Longterm follow up of patients surgically treated by the far lateral approach for foraminal and extraforaminal lumbar disc herniations. J Neurosurg: Spine 90: 59-66, 1999.<br />
Reulen H-J, Milller A, Ebeling U. Microsurgical anatomy of the lateral approach to extraforaminal lumbar disc herniations. Neurosurgery 39: 345­351, 1996.<br />
8.. Wiltse LL, Bateman JG, Hutchinson RH, Nelson WE. The paraspinal sacrospinalis-splitting approach to the lumbar spine. J Bone Joint Surg 50A: 919-926, 1968.<br />
Wiltse LL, Guyer RD, Spencer CW, Glenn WV, Porter IS. Alar tranverse process impingement of the L5 spinal nerve: The far-out syndrome. Spine 9: 31-41, 1984.<br />
Zonenshayn M, Edger MA, Lavyne MH. Removal of a lumbar melanotic schwanoma vía the far lateral approach in a patient with Carney complex. Case report. J Neurosurg: Spine 92: 241­245, 2000.]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1297">
    <dcterms:title><![CDATA[Epilepsia extratemporal<br />
Selección del candidato y tratamiento quirúrgico]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Artículo Original]]></dcterms:description>
    <dcterms:abstract><![CDATA[Se analizan los resultados obtenidos en 60 niños y 8 adultos con diagnóstico de epilepsia extratemporal operados entre 1988 y 1998 con un seguimiento mayor de 2 años. Todos fueron estudiados con TAC e IRM y EEG de cuero cabelludo. La Videotelemetría, ECoG intraoperatoria y la PESS se utilizaron de acuerdo con las necesidades de cada caso. En los niños se efectuaron 24 lesionectomías, 25 desconexiones, 7 polectomías y / o lobectomías, 1 hemisferectomía y 3 corticectomías. En los adultos se efectuaron 1 lobectomía, 4 corticectomías y 3 lesionectomías. De acuerdo con los criterios de Engel, en los niños los resultados fueron: 40 clase I, 5 clase II y 4 clase IV. En los adultos los resultados fueron: 4 clase I, 2 clase II, 1 clase III y 1 clase IV. Se excluyeron 11 pacientes con callostomías por no poder aplicar los criterios de Engel.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[We analyzed the outcome in 60 children and 8 adults with extratemporal epilepsy operated between 1988-1998 and a follow-up of more than 2 years. AU patients were studied with CAT, MRI and scalp EEG. Video-telemetry, intraoperative ECoG and SSEP were used according to the needs of each case. In children were performed 24 lesionectomies, 25 disconnections, 7 polectomies and/ Or lobectomies, 1 hemispherectomy and 3 corticectomies. In the adults we performed 1 lobectomy, 4 corticectomies and 3 lesionectomies. According with Engercriteria, the surgical results in children were: 40 class I, 5 class II and 4 class N. In the adults the surgical results were: 4 class I, 2 class II, 1 class III and 1 class IV We excluded 11 patients with callostomies because Engel&#039;criteria could not be applied.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Hugo B. Pomata]]></dcterms:creator>
    <dcterms:publisher><![CDATA[León Turjanski]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2000]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[Awad IA, Wyllie E, Lüders HO, Hal J. Intraoperative determination of corpus callosotomy for epilepsy: two simple techniques. Neurosurgery 26: 102­106, 1990.<br />
Barnett GH, Burgess R, Awad IA, Skipper GJ, Edwards CR, Lüders HO. Epidural PEG electrodes for presurgical evaluation of intractable epilepsy. Neurosurgery 27: 113-115, 1990.<br />
Cahan LD, Sutherling W, Mc Coullogh AM, Rausch R, Engel J, Crandall PH, Review of 20 years UCLA experience with surgery for epilepsy. Cleve Clin Q 51: 313-318, 1984.<br />
Cataltepe O, Comair Y. Complications of extratemporal epilepsy surgery in infants and children. En: Pediatric epilepsy syndrome and their surgical treatment. Cap 72 pág. 709-725. Editor: I. Tux­horn- H. Holthausen- H. Boenigk. John Libbey. London. England. 1997.<br />
Comair Y, Choi HY, Van Ness P. Neocortical resections. In Epilepsy- A comprehensive textbook. Vol 2. Cap 171 pág. 1820. Editor: J. Engel (Jr). Timothy A. Padley. Lippincott-Raven Presss. 1998.<br />
Comair Y, Choi HY, Van Ness P. Neocortical resections. In Epilepsy- A comprehensive textbook. Vol. 2. Cap. 171 pág. 1.825. Editor J. Engel (Jr). Timothy A. Padley- Lippincott- Rayen Press. 1998.<br />
Jean-Pierre Farmer. Operative strategies in the management of extratemporal epilepsy of childho­od. Chap 70 pág. 691-695. En: Paediatric Epilepsy Syndromes and their Surgical Treatment. I. Editors Tuxhorn, H. Holthausen, H. Boenigk. Published by John Libbey Company Ltd. London. England. 1997.<br />
Farmer SF, Harrison LM, Stevens JA. Plasticity of central motor pathways in children with hemiplegic cerebral palsy. Neurology 41: 1.505-1.510, 1991.<br />
R. García de Sola. Exploración del paciente epiléptico con electrodos intracraneales. Cap. 15. En: Tratamiento de la epilepsias. Editor Francisco Villarejo. Díaz Santos. Madrid. 1998.<br />
García MC, Tenca E, Pomata HB, Stelles S, Cervio A, D&#039;Gianno C, Rabinowicz A. Utilidad de la electrocorticografia para definir área epilpetogénica en pacientes epilépticos sometidos a cirugía. &#039;Crisis 4: 5-12, 1998.<br />
Gorman D, Shields D, Sherwalon A, Chugani H, Finker R, Comair Y, Peackock W. Neurosurgical treatment of refractory status epilepticus. Epilepsia 33: 516-519, 1992.<br />
Kaufmann W, Krauss GL, Vematsu S, Lesser R. Treatment of epilepsy with multiple subpial transections: an acute histologic analysis in human subjects. Epilepsia 37: 342-352, 1996.<br />
Morrell F, Whisser WW, Bleck TP, Multiple subpial transection: a new approach to the surgical treatment of focal epilepsy. J. Neurosurgery 70: 231­239, 1989.<br />
André Olivier M.D., Ph. D. FRCS (C) Surgery of Epilepsy. Oyeran procedure. Pág. 38-43. Montreal Neurological Hospital and Institute. Mc Gill University. Montreal. Quebec. Canadá. 1995.<br />
Peacock WJ, Comair Y, Chugani HT, Shewmon DA, Shields WD. Epilepsy surgery in childhood Chap 66. Pag. 589-598. En: Epilespy Surgery . Editor J. Engel (Jr) 2a.. ed. Rayen Press. N.Y. 1992.<br />
Peacock WJ, Comair Y, Hoffman H, Montes JL, Morrison G. Special considerations for epilepsy surgery in childhood. Cap 46pág. 541-547. En: Surgical Treatment of epilepsies. Editor J. Engel (Jr) 2a. ed.Raven Press. N.Y. 1993.<br />
Pomata H, Delalande O, González R, Monges J. Hemisferotomía como tratamiento de la encefalitis de Rasmusen. Rev Argent de Neuroc 9: 153-159, 1995.<br />
Pomata H, Waisburg H, Medina C. Epilepsias extratemporales. Cap. 17 pág. 295-320. En: Tratamiento de la Epilepsia. Editor Francisco Villarejo Ortega. Editorial Díaz de Santos. Madrid. 1998.<br />
Prats AR, Morrison G, Wolf A. Focal cortical resections for the treatment of extratemporal epilepsy in children. Neurosurgery Clin North Am 6: 533­534, 1995.<br />
Sisodiya SM, Moran N, Free SL, Kitchen ND, Stevens JM, Harkness WFJ, Fish DR, Shervo Sd. Correlation of widespread preoperative magnetic resonance Imaging changes with unsuccessful surgery for hippocampal sclerosis. Ann Neurol 41: 490-496, 1997.<br />
Stephan H, Quesney LF, Feister HK, Schüler P, Wies m, Hurnmer C. Pauli E. Presurgical evaluation in frontal lobe epilepsy. A multimethodological approach. Cap 15. En: Epilepsy and the functional anatomy of the frontal lobe. Editors: Jasper H. H., Riggio S. and Goldmanrakic P.S. Rayen Press Ltd. N.Y. 1995.<br />
Valenzuela JM, Cristante L, Damman O, Bentele K, Vortmeyer A, Saeger W, Padberg B, Freitas J, Herrmann HD: Hypothalamic hamartoma: with special reference to gelastic epilepsy and surgery. Neurosurgery 34: 949-958, 1994.<br />
Ventureyra EG, Higgins MJ. Complications of epilepsy surgery in children and adolescents. Pediatr Neurosurg 19: 40-56, 1993.<br />
Villemure JG, Rasmussen T. Functional hemispherectomy. methology. J. Epilepsy 3 (Suppl): 177­182, 1990.<br />
Zeller JA, Schlesinger S, Runge U, Kessler C. Influence of valproate monotherapy on platelet activation and hematologic values. Epilepsia 40: 186-189, 1999.<br />
Zentner J, Hufnagel A, Ostertun B, Wolf HK, Behrens E, Campos MG, Solymosi L, Elger C, Wiestler OD, Schanan J. Surgical treatment of extratemporal epilepsy: clinical, radiologic and histopathologic findings in 60 patients. Epilepsia 37: 1072­1080, 1996.<br />
]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1296">
    <dcterms:title><![CDATA[Aneurismas intracraneanos<br />
Nuestra experiencia en 53 casos operados en 3 años]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Artículo Original]]></dcterms:description>
    <dcterms:abstract><![CDATA[Se realizó una revisión clínico-quirúrgica de 53 casos operados por aneurismas intracraneales entre enero de 1997 y diciembre de 1999.<br />
Objetivos: analizar las relaciones entre la gradación de Hunt-Hess, la escala de Fisher tornográfica, la incidencia de vasoespasmo , la estrategia y la técnica quirúrgica como factores relevantes en la evolución.<br />
Material y métodos: nuestros 53 pacientes se distribuyeron de la siguiente manera:<br />
- Score de Hunt-Hess : grado O: un paciente ; grado I : 17 pacientes ; grado II: 25 pacientes; grado III: 8 pacientes; grado IV ninguno, y grado V :un paciente.<br />
- Escala de Fisher: grado I: 3 casos ; grado II: 28 casos, grado III : 11 casos y grado IV: 11 casos.<br />
- Vasoespasmo clínico y / o angiográfico : en 17 pacientes.<br />
- Estrategia quirúrgica: cirugía precoz en 25 casos.<br />
Resultados: la mortalidad en los casos con Hunt-Hess grados 1 y 2 fue del 2,7%, en 33 pacientes se constató una muy buena evolución y en 8 casos una buena evolución. La mortalidad fue del 50 % en los grados 3 a 5.<br />
Conclusión: se observó evolución favorable en los pacientes intervenidos con Hunt­Hess 1 y 2, en comparación con aquellos en grados 3 a 5. Se evidencia como elemento singular relevante en el pronóstico el nivel de conciencia prequirúrgico con respecto a las demás variables.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[A clinical surgical review of 53 cases of intracranial aneurysms operated on from January 1997 to December 1999 was performed.<br />
Objetives: To analyze the relationship between the Hunt and Hess grading system, Fisher tomographic scale, vasospasm incidence, surgical strategy and technic as relevant factors in patient outcome.<br />
Material and Methods: Our 53 patients showed the following distribution :<br />
- Hunt and Hess grade 0: one patient; grade I: 17 patients; grade II: 25 patients; grade III: 8 patients; grade IV: none and grade V: 1 patient.<br />
- Fisher scale. Grade I: 3 cases; grade II: 28 cases; grade III: 11 cases and grade IV: 11 cases. Clinical and/ or angiographic vasospasm: 17 patients.<br />
- Surgical strategy: early surgery in 25 cases.<br />
Results: Patients belonging to Hunt and Hess grades 1 and 2 had a 2.7% mortality rate with a very good outcome in 33 cases and good outcome in 8. Grades 3 to 5 had an overall mortality of 50%.<br />
Conclusion: A good outcome was observed in patients included in Hunt and Hess grades 1 and 2 as compared to patients in grades 3 to 5. Furthermore, the patients presurgical consciousness level resulted in the single most important prognostic factor.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Ignacio Mendiondo ]]></dcterms:creator>
    <dcterms:creator><![CDATA[Eulogio Mendiondo]]></dcterms:creator>
    <dcterms:publisher><![CDATA[León Turjanski]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2000]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[Awad I, Carter LP, Spetzler RF, Medina M, Williams FW: Clinical Vasospasm After Subarachnoid Hemorrhage: Response to Hipervolemic Hemodilution and Arterial Hypertension. Stroke 18: 365­372, 1987.<br />
Aring CD: A medical perspective. Neurology 34: 1.357-1.361, 1984.<br />
Bailes JE, Spetzler RF,Hadley MN et al: Management morbidity and mortality of poor-grade aneurysm patients. J Neurosurg 72: 559-566, 1990.<br />
Chyatte D, Fode NC, Sund TM Jr: Early versus late intracraneal Aneurysm Surgery in Subarachnoid Hemorrhage. J Neurosurg 69: 326-331,1988.<br />
Duke BJ, Kindt GW y Breeze RE: Outcome after urgent surgery for grade IV subarachnoid hemorrhage. Surg Neurol 50: 169-173, 1998.<br />
Fisher CM, Kistler JP y Davis JM: Relation of cerebral vasospasm to subarachnoid Hemorrhage visualized by Computerized Tomographic Scanning. Neurosurg 6: 1-9,1980.<br />
Fleischer AS y Tindall GT: Cerebral vasospasm following aneurysm rupture. J Neurosurg 52: 149­152,1980.<br />
Fontana H, Belziti H Mendiondo 1: El Colgajo Orbitocigomático: Reflexión anatómica y nota técnica. RevArgent de Neurocirugía 9: 160-164,1995.<br />
Gilsbach JM, Reulen HJ, Ljunggren B y col: Early Aneurysm Surgery and Preventive Therapy with intravenously Administered Nimodipine: A Multicenter. Double-Blind, Dose- Comparison Study. Neurosurg 26: 458-464,1990.<br />
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Kassel NF, Torner JC, Haley EC, Jane JA et al: The International Cooperative Study on the timing of Aneurysm Surgery. Part 1: Overall management results. J Neurosurg 73: 18-36, 1990.<br />
Kassel NF Torner JC, Jane JA et al: The International Cooperative Study on the Timing of Aneurysm Surgery. Part 2: Surgical Results. J Neurosurg 73: 37-47, 1990.<br />
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Ohman J, Servo A y Heiskanen O: Risks Factors for cerebral infarction in good grade patients after aneurysm subarachnoid hemorrhage and surgery: a propective study. J Neurosurg 74: 12-20, 1991.<br />
Oliveira E, Tedeschi H, Siqueira MG y Peace DA: The pretemporal Approach to the Interpeduncular and petroclival regions. Acta Neurochirurglca 136: 204-211,1995.<br />
Saladino P, Viano JC, Suarez JC y Herreran EJ: Nuestra experiencia en el manejo de los aneuris­mas intracraneanos. Rey, Argent de Neurocirugía vol 9: 1-8, 1995.<br />
Selles S, Knezevich F, Ferrari R, Malach I, Gregori M, Konsol C y Ciraolo C: Tratamiento quirúrgico de los aneurismas cerebrales: Trabajo Cooperativo. Rey Argent de Neurocirugía 9: 97-101,1995.<br />
Taneda M: The significance of early operation in the management of ruptured intracranial neurysms­and analysis of 251 cases hospitalized within 24 hours after subarachnoid hemorrhage. Acta Neu­rochir (Win) 63: 201-208,1982.<br />
Vishteh AG, Marciano FF, David CA, Basldn JJ y Spetzler RF: The Pterional Approach. Operative Techniques in Neurosurgery 1: 39-49,1998.<br />
Yasargil MG y Fox JL: The Microsurgical Approach to Intracranial Aneurysms. Surg Neurol 3: 7-14, 1975.<br />
Yoshimoto Y, Wakai S, Satoh A et al: A prospective Study on the effects of Early Surgery on vasospasm after subarchnoid Hemorrhage. Surg Neurol 51: 392-398,1999.<br />
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Zervas NT, y Ogilvy CS: Contemporary Management of vasospasm. Clinical Neurosurgery 20: 167 174,1997.]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1295">
    <dcterms:title><![CDATA[Tratamiento quirúrgico de los cavernomas del tronco encefálico]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Actualización]]></dcterms:description>
    <dcterms:abstract><![CDATA[Los cavernomas ubicados en el tronco encefálico pueden provocar hemorrgias a repetición con secuelas neurológicas significativas. Si bien el tratamiento es dicutido, actualmente los autores recomiendan la resección quirúrgica de las lesiones abordables, cuando hayan presentado hemorragia o déficit progresivo debido al incremento del tamaño. El papel de la radiocirugía no está aún claro y hay autores que la contraindican.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Brain stem cavernomas can bleed repeatedly causing significative neurological sequelae in spite that their treatment is controversial, most authors recommend surgery when cavernomas bleed, have a progressive defieit and/ or are easy to approach. The role of radiosurgery is not clear and some authors think that is contraindicated.<br />
]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Federico C. Viñas<br />
]]></dcterms:creator>
    <dcterms:creator><![CDATA[Vickie Gordon y]]></dcterms:creator>
    <dcterms:creator><![CDATA[Fernando G. Díaz]]></dcterms:creator>
    <dcterms:publisher><![CDATA[León Turjanski]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2000]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[1.	Abdulrauf SI, Kaaynar MY, Awad IA et al: A comparison of the clinical profile of cavernous mal¬formations with and without associated venous malformations. Neurosurgery 44: 41-46, 1999.<br />
2.	Abe H: Clinical presentation of vascular malforma¬tions in the brainstem: Comparison of angiografica¬lly positive and negative types. J Neurol Neurosurg Psych 52: 167-175, 1989.<br />
3.	Abe M, Ogawa A, Yoshida Y et al: Surgical removal of cavernous angioma in the medulla oblongata. A case report. Neurosurg 20: 128-131, 1997.<br />
4.	Acciarri N, Padovani R, Giulioni N et al: Intracranial and orbital cavernous angiomas: a review of 74 surgical cases. Br J Neurosurg 7: 529-539, 1993.<br />
5.	Agnoli AL: Neuroradiologic study using modem imaging procedures (CT: NMR) in venous, cerebral vascular malformations. Neurochirurgia (Stuttg). 29: 225-229, 1986.<br />
6.	Ahmadi J, Miller CA, Segall AD et al: CT patterns in histopathologically complex cavernous hemangio¬mas. AJNR 6: 389-393, 1985.<br />
7.	Aiba T, Tanaka R, Koike T et al: Natural history of intracranial cavernous malformations. J Neuro¬surg 83: 56-59, 1995.<br />
8.	Alexander E, LoeffierJS: Radiosurgery for intracranial vascularmalformations: Techniques, results, and complications. Clin Neurosurg 39: 273-291, 1992.<br />
9.	Alexander E, Loeffer JS: Radiosurgery using a modi¬fied linear accelerator. Neurosurg Clin N Am 3: 167-190, 1992.<br />
10.	Alvarez-Sabin J, Montalván J, Tintore Metal:  Pure sensory stroke due to midbrain haemorrhage. J Neurol Neurosurg Psychiatry 54: 843, 1991.<br />
11.	Amin-Hanjani S, Ojilvy CS, Canadia G, et al: Stereo¬tactic radiosurgery for cavernous malformations: Kjellberg&#039;s experience with proton bean therapy in 98 cases at the Harvard cyclotron. Neurosurgery 1229-1237, 1998.<br />
12.	Arutiunov Al, Korninko VN: Catheterization cere¬bral angiography in the diagnosis of vascular lesions of the brain. Vopr Neirokhir 33: 11-16, 1969.<br />
13.	Awad IA, Robinson JR et al: Comparison of the clinical presentation of symptomatic arteriovenous malformations and occult vascular malformations. Neurosurgery 32: 876-878, 1993.<br />
14.	Awad IA, Robinson JR, Mohanty S et al: Mixed vascular malformations of the brain: clinical and pathogenetic considerations. Neurosurgery 33: 179-188, 1993.<br />
15.	Basauri L, Rocamora RJ: Cavernomas. Report of two cases. Neurocirugía 23: 77-78, 1965.<br />
16.	Bentley CR, Bronstein AM, Paldon N et al: Fast eye movement initiation of ocular torsion in mesodien¬cephalic lesions. Ann Neurol 43: 729-737, 1998.<br />
17.	Berry R, Alpers B, White J: The site, structure, and frequency of intracranial aneurysms, angiomas, and arteriovenous abnormalities. En: Milikan C (ed): Research Publications: Association for Resear¬ch in Nervous and Mental Disease. Baltimore: Willia¬ms &amp; Willdns, pp. 4-72, 1966.<br />
18.	Bertalanffy H, Gilsbach JM, Eggert HR et al: Microsur¬gery of deep-seated cavernous angiomas: report of 26 cases. Acta Neurochir (Wien.) 108: 91-99, 1991.<br />
19.	Bicknell JM, Carlow TJ, Kornfeld M et al: Familial cavemous angiomas. Arch Neurol 35: 746-749, 1978.<br />
20.	Bicknell JM: Familia&#039; cavernous angioma of the brain stem dominantly inherited in Hispanics. Neu¬rosurgery 24: 102-105, 1989.<br />
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43.	Fahlbusch R, Strauss C, Huk W: Pontine-mesence¬phalic cavernomas: indications for surgery and operative resulta Acta Neurochir 53:37-41, 1991,<br />
44.	Fahlbusch R, Strauss C, Huk W: Pontine-mesence¬phalic cavernomas: indications for surgery and operative results, Acta Neurochlr 53:37-41, 1991,<br />
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46.	Fukui M, Matsushima T, Ikezaki K et al: Surgery of angiomas in the brainstem with a stress on the presence of telangiectasia, Neurol Med Chir (Tokyo) 38 Suppl: 250-254, 1998,<br />
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]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1294">
    <dcterms:title><![CDATA[EDITORIAL]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Editorial]]></dcterms:description>
    <dcterms:creator><![CDATA[León Turjanski]]></dcterms:creator>
    <dcterms:publisher><![CDATA[León Turjanski]]></dcterms:publisher>
    <dcterms:date><![CDATA[Octubre 2000]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1293">
    <dcterms:title><![CDATA[EDITORIAL]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Editorial]]></dcterms:description>
    <dcterms:creator><![CDATA[Álvaro Campero]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Diciembre 2019]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1292">
    <dcterms:title><![CDATA[Introducción a la Neurocirugía]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Novedades Editoriales]]></dcterms:description>
    <dcterms:creator><![CDATA[Juan José Mezzadri]]></dcterms:creator>
    <dcterms:creator><![CDATA[Javier Goland]]></dcterms:creator>
    <dcterms:creator><![CDATA[ Mariano Socolovsky]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Diciembre 2019]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1291">
    <dcterms:title><![CDATA[Schwannomatosis del nervio plantar interno.<br />
Presentación de caso<br />
Premio Póster. XV Jornadas de Neurocirugía 2019]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Trabajos Premiados]]></dcterms:description>
    <dcterms:abstract><![CDATA[Introducción: Las Schwannomatosis Mononeurales de los Miembros son entidades muy poco frecuentes, escasamente<br />
conocidas y raramente publicadas en la bibliografía internacional, éstas se encuentran caracterizadas por la existencia de<br />
múltiples formaciones nodulares o plexiformes con compromiso exclusivo de un solo nervio, todas con diagnóstico patológico<br />
de schwannoma, excluyéndose a otras entidades tumorales y fuera del contexto de una neurofibromatosis. Aquí se presenta<br />
un caso con compromiso del nervio plantar medial o interno.<br />
Material y método: Se evaluó y analizo el caso clínico, a nivel semiológico y Neurorradiológico, Neurofisilógico. Se definió la<br />
conducta terapéutica y quirúrgica. Se evaluaron resultados mediante: análisis semiológico y seguimiento con imágenes.<br />
Descripción y resultados: Paciente sexo masculino de 45 años de edad consulta por presentar múltiples tumoraciones palpables<br />
en región retromaleolar interna y plantar derecho y disestesias al apoyo, con antecedente de cirugía de schwannoma plantar. Al<br />
examen neurológico: masas palpables en los sectores previamente indicados y Tinel a nivel retromaleolar interno y plantar.<br />
RMN: múltiples nódulos con captación intermedia de contraste, hipertensos en T2.<br />
Se practicó resección quirúrgica mediante amplio abordaje, se identificaron múltiples nódulos, uno de ellos de aspecto<br />
plexiforme que involucraba la totalidad del nervio plantar interno imposibilitando la preservación del tronco por lo cual se<br />
practicó microneurorrafia con interposición de puente de safeno interno.<br />
Discusión y conclusión: Las Schwannomatosis Mononeurales de los Miembros son entidades extremadamente raras, se han<br />
reportado con una frecuencia un poco mayor a aquellas que involucran a los nervios mediano y cubital, en sus características<br />
macroscópicas las lesiones fueron publicadas como pertenecientes a la variante nodular para esa escasa mayoría. La<br />
configuración plexiforme de los schwannomas es menos frecuente que la nodular per se y, en general. está asociada a<br />
troncos menores, fuera de estos territorios, su rareza es extrema. Este caso clínico resulta aún más especial por tratarse de<br />
una Schwannomatosis Mononeural del Plantar Medial con variante de tipo mixto, es decir nodular con una masa plexiforme<br />
dominante. Esta entidad no la hemos encontrado en la bibliografía internacional.<br />
Por otro lado, la resección quirúrgica de estos tumores, cuando son nodulares es compatible con la preservación del tronco<br />
nervioso, sacrificando solamente, su fascículo de origen. Este caso, dada la configuración descripta del tumor principal, el cual<br />
involucraba la totalidad del tronco, se hizo imposible la preservación del nervio, para lo cual debió realizarse microneurorrafia<br />
con puente. Como consideración final, creemos que es de capital importancia la adecuada exploración y planificación pre e<br />
intraoperatoria de estos pacientes.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Introduction: Mononeural Schwannomatosis located at limbs are very infrequent entities, the knowledge about its are very<br />
poor, and there are just a few publications related to them. This articles make reference multiple nodular or plexiform lesions<br />
with involvement oh only one nerve, every one whit diagnosis of schwannoma, excluding fibromatosis. In this article, we<br />
describe a patient with who suffered the involvement of multiples tumours with nodular and plexiform configuration.<br />
Material y method: The clinical case was analysed by different media, clinical, neuro physiological and by neuroimages. By this<br />
approaches were defined and evaluated the surgical outcomes and results.<br />
Clinical case: Male, 45 years old. Multiples tumours at plantar region. Tinel Sign with multiple palpable masses al retromaleolar<br />
sulcus and plantar region, plantar schwannoma operated on previously.<br />
RMN: multinodular configuration at level of medial plantar nerve, with intermediate contrast reinforcement.<br />
An extended approach was performed, from retromaleolar sulcus to medial aspect of the foot, and finishing inside the digitalplantar<br />
sulcus. Complete resection was performed, multiples nodulos were found, the bigger had a plexiform configuration, was<br />
imposible the preservation of the nerve trunk and the, the interposition of sural nerve was realized. With good evolution<br />
Conclusions: For this very rare entities, the bigger frequency was reported et limbs.<br />
The most frequent locations was at medial nerve, second place occupied by the ulnar nerve, we didn’t find on international<br />
literature a plexiform tumour inside the medial plantar nerve.<br />
On the other hand, we think that the complete resection for this tumours when are nodular, the complete resection with<br />
preservation of the main trunk, is feasible. Ehen the tumour has a plexiform pattern; complete resection is only feasible with<br />
trunk nerve resection and interposition of nerve graft.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Luis Mariano Cuello]]></dcterms:creator>
    <dcterms:creator><![CDATA[Leonardo Guidobono]]></dcterms:creator>
    <dcterms:creator><![CDATA[Betiana Arnaudin]]></dcterms:creator>
    <dcterms:creator><![CDATA[Carlos Llerena]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Diciembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Agosto 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Agosto 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:references><![CDATA[1. Angelini A1, Bevoni R, Biz C, Cerchiaro MC, Girolami M, Ruggieri<br />
P.Schwannoma of the foot: report of four cases and literature review.<br />
Acta Biomed. 2019 Jan 10;90(1-S):214-220. doi: 10.23750/abm.<br />
v90i1-S.8079.<br />
2. Li XN, Cui JL, Christopasak SP, Kumar A, Peng ZG.Multiple<br />
plexiform schwannomas in the plantar aspect of the foot: case<br />
report and literature review.BMC MusculoskeletDisord. 2014 Oct<br />
11;15:342. doi: 10.1186/1471-2474-15-342.<br />
3. Gosk J, Gutkowska O, Urban M, Wnukiewicz W, Reichert P,<br />
Ziółkowski P.Results of surgical treatment of schwannomas<br />
arising from extremities.Biomed Res Int. 2015;2015:547926. doi:<br />
10.1155/2015/547926. Epub 2015 Feb 22.<br />
4. MarkosIoannou, 1 Ioannis Papanastassiou,1 Ioanna<br />
Iakowidou,2 Stamatios Kottakis,1 and NikolaosDemertzis.<br />
Plexiformschwannoma of the posterior tibial nerve: a case report.<br />
Published online 2009 Aug 17. doi: 10.4076/1757-1626-2-8392.<br />
5. Touteréférence à cet article doit porter la mention :Valeyrie-Allanore<br />
L., Wolkenstein P. Neurofibromatose 1 et formesvariantes. EMC<br />
(ElsevierMassonSAS,Paris), Neurologie, 17-170-A-65, 2009.<br />
6. Nafiseh Mortazavi, Kambiz Novin Farahnaz Bidari Zerehpoosh,<br />
Managol Sadatsafavi. Plexiform Schwannoma of the Finger: A<br />
Case Report and Literature Review.Departments of Pathology and<br />
Clinical Oncology, Shahid Beheshti University of Medical Sciences,<br />
Tehran, Iran. July 4, 2019, IP: 181.167.224.166.]]></dcterms:references>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1290">
    <dcterms:title><![CDATA[Cirugía de oberlin en parálisis braquial obstétrica.<br />
Nota técnica<br />
Premio Junior. XV Jornadas Argentinas de Neurocirugía 2019]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Trabajos Premiados]]></dcterms:description>
    <dcterms:abstract><![CDATA[Introducción: La parálisis braquial obstétrica (PBO) constituye una complicación poco frecuente del parto. La mayoría de<br />
los pacientes recuperan espontáneamente, sin embargo en algunos casos debe realizarse una neurocirugía para reinervar<br />
músculos y restablecer funciones. Las ramas mayoritariamente afectadas son C5-C6. Oberlin describió por primavera vez un<br />
tipo de trasferencia nerviosa en 4 pacientes adultos, utilizando fascículos del nervio ulnar para reanimar el músculo bíceps. El<br />
objetivo de este trabajo consiste en realizar una nota técnica sobre la cirugía de Oberlin, en el contexto de una PBO. Esta nota<br />
técnica surge del análisis de 4 cirugías pediátricas y de las disecciones de 14 miembros superiores fetales.<br />
Descripción técnica: Paciente en decúbito dorsal, con el brazo afectado extendido, en supinación y abducción de 90°. Se<br />
incide piel 4cm de extensión en cara interna del brazo, hasta identificar la fascia braquial. Posteriormente se diseca la rama<br />
motora del bíceps y fascículos del ulnar. Mediante magnificación se aproximan los cabos y se realiza la neurorrafia.<br />
Discusión: Existen múltiples técnicas descriptas de transferencia nerviosa, escasa es la bibliografía en pacientes pediátricos.<br />
La cirugía de Oberlin puede ser realizada en pediatría.<br />
Conclusión: Presentamos los pasos de la cirugía de transferencia nerviosa descripta por Oberlin, la misma es reproducible<br />
en pacientes lactantes en contexto de PBO, quedando expuestos los detalles técnicos y los reparos anatómicos para su<br />
realización.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Introduction: Obstetrical brachial plexus palsy (OBPP) is a rare complication of labor. Most patients recover spontaneously,<br />
however, in some cases neurosurgery must be perform to re innervate muscles and restore functions. The most frequent<br />
affected roots are C5-C6. Oberlin first described a type of nervous transfer in 4 adult patients, using fascicles of the ulnar nerve<br />
to reanimate the biceps muscle. The objective of this paper is to make a technical note about Oberlin&#039;s surgery regarding<br />
OBPP. This technical note emerges from the analysis of 4 pediatric surgeries and 14 fetal upper limbs dissections.<br />
Technical description: Patient was place in dorsal decubitus, with the compromised upper limb extended in supination and<br />
90 ° abduction. Skin incision of 4 cm long is made along the medial aspect of the arm, until the brachial fascia is identified.<br />
Subsequently, the motor branch of the biceps muscle and fascicles of the ulnar nerve are dissect. Under microscopic<br />
magnification, both nerves are approached and the neurorrhaphy is performed.<br />
Discussion: There are multiple nerve transfer techniques described; but bibliography in pediatric patients is limited. Oberlin<br />
surgery can be performed in pediatrics.<br />
Conclusion: The steps of the nerve transfer surgery described by Oberlin presented can be applied in the case of obstetrical<br />
brachial plexus palsy, the technical details and the anatomical repairs for its realization are outlined.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Luciano Grisotto]]></dcterms:creator>
    <dcterms:creator><![CDATA[Jorge Luis Bustamante]]></dcterms:creator>
    <dcterms:creator><![CDATA[Gonzalo Colombo]]></dcterms:creator>
    <dcterms:creator><![CDATA[ Carolina Maldonado<br />
]]></dcterms:creator>
    <dcterms:creator><![CDATA[Nicolas Tello]]></dcterms:creator>
    <dcterms:creator><![CDATA[Fernando Torres]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Diciembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Agosto 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Agosto 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
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CIRUGÍA DE OBERLIN EN PARÁLISIS BRAQUIAL OBSTÉTRICA. NOTA TÉCNICA<br />
Luciano Grisotto, Jorge Luis Bustamante, Gonzalo Colombo, Carolina Maldonado, Nicolas Tello, Fernando Torres<br />
REV ARGENT NEUROC. | 2019 TRABAJO PREMIADO<br />
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AS. Non-Sedated Rapid Volumetric Proton Density MRI Predicts<br />
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    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1289">
    <dcterms:title><![CDATA[¿Cómo entrenar para el uso del exoscopio?<br />
Utilización de un novedoso simulador de exoscopía<br />
de bajo costo por residentes de neurocirugía<br />
Premio Beca AANC-FLANC. XV Jornadas de Neurocirugía 2019 de AANC]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Trabajos Premiados]]></dcterms:description>
    <dcterms:abstract><![CDATA[Introducción: Analizar el impacto del entrenamiento en una estación de simulación en exoscopía (ESA) de bajo costo, utilizado<br />
por un grupo de residentes de neurocirugía.<br />
Materiales y métodos: Se reclutaron 6 residentes de neurocirugía, todos ellos sin experiencia previa en exoscopía. Se<br />
desarrolló una estación de simulación en exoscopía compuesta por una computadora, una webcam y una fuente de luz.<br />
Todos los participantes realizaron un tutorial introductorio, un ejercicio inicial de 5 suturas (cada sutura fue clasificada en forma<br />
binaria como correcta e incorrecta), evaluando el tiempo necesario para completar dicho ejercicio y la eficacia (definida como<br />
la relación entre suturas correctas y el total). Posteriormente se realizaron 3 sesiones de entrenamiento semanal de 1 hora<br />
cada una y una evaluación final con las mismas características que la inicial. Ambas evaluaciones fueron estudiadas por un<br />
neurocirujano senior que realizó un análisis, así como la puntuación de cada ejercicio de los participantes.<br />
Resultados: El tiempo promedio de realización del ejercicio inicial fue de 31 minutos con 59 segundos, con una eficacia<br />
promedio del 70%. Luego del entrenamiento el promedio de tiempo fue 18 minutos y 12 segundos, con una eficacia del 80%.<br />
Conclusión: El entrenamiento en este simulador demostró una notable mejoría en los tiempos y la calidad de la técnica<br />
exoscópica si se compara el principio del entrenamiento con su final. Por los beneficios obtenidos y su bajo costo creemos<br />
que será útil su implementación para acercar dicha técnica a todos los neurocirujanos que se encuentren interesados en ella.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Introduction: To analyze the impact of training in a low-cost simulation station of exoscopy, used by residents of neurosurgery.<br />
Materials and methods: Six residents of neurosurgery were recruited, all of them having no previous experience in the use<br />
of the exoscope. An exoscopy simulation station, including a computer, a webcam and a light source, was developed. All<br />
the participants performed an introductory tutorial, an initial exercise of 5 sutures (each suture was classified as correct and<br />
incorrect), evaluating the time to complete this exercise and the efficacy (defined as the relation between correct sutures and<br />
the total). Posteriorly, 3 training sessions of 1 hour and a final evaluation with the same characteristics as the initial one were<br />
performed by all the participants. Both evaluations were studied by a senior neurosurgeon who gave individualized punctuation<br />
and feedback to the participant.<br />
Results: The average time of the initial exercise was 31 minutes 59 seconds, with an average efficiency of 70%. After training,<br />
the average time was 18 minutes, 12 seconds, with an efficiency of 80%.<br />
Conclusion: The simulator training demonstrated the improvement of the exoscopic technique of the evaluated residents.<br />
Because of the benefits that were observed, and also its low cost, we believe that the implementation of this device will be<br />
useful to all neurosurgeons interested in this technique.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Ezequiel Yasuda]]></dcterms:creator>
    <dcterms:creator><![CDATA[ Federico Minghinelli]]></dcterms:creator>
    <dcterms:creator><![CDATA[Daniela Renedo]]></dcterms:creator>
    <dcterms:creator><![CDATA[Pablo Devoto]]></dcterms:creator>
    <dcterms:creator><![CDATA[ Lucas Pina]]></dcterms:creator>
    <dcterms:creator><![CDATA[Ana Lovaglio]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Diciembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Agosto 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Agosto 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:references><![CDATA[1. Birch K, Drazin D, Black KL, Williams J, Berci G, Mamelak AN.<br />
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Infratentorial supracerebellar resection of a pineal tumor using a<br />
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nephrectomy: initial clinical experience. Urology 2009;73:302–5.<br />
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wing infusion model. Surgical Neurology 2009;72(6), 695–9.<br />
doi:10.1016/j.surneu.2008.12.008.<br />
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A, Malheiros JA, Nakaji P. Human Placenta Aneurysm Model for<br />
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16. Parihar V, Yadav YR, Kher Y, Ratre S, Sethi A, Sharma D. Learning<br />
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17. Ricciardi L, Chaichana KL, Cardia A, Stifano V, Rossini Z, Olivi A,<br />
Sturiale CL. The exoscope in neurosurgery: an innovative “point of<br />
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present, and future. Neurosurgical Focus 2009; 27(3), E4.doi:10.31<br />
71/2009.6.focus09120.]]></dcterms:references>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1288">
    <dcterms:title><![CDATA[RODEXKE. Infiltración con ropivacaína,<br />
dexmedetomidina y ketorolac en cirugía espinal:<br />
Una estrategia para disminuir el consumo de opioides<br />
2do Premio Beca Asociación Argentina de Neurocirugía.<br />
XV Jornadas de Neurocirugía 2019]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Trabajos Premiados]]></dcterms:description>
    <dcterms:abstract><![CDATA[Objetivos: Evaluar la efectividad de la infiltración del sitio quirúrgico, con ropivacaína, dexmedetomidina y ketorolac, en<br />
pacientes sometidos a instrumentación transpedicular dorsolumbar con técnica mini invasiva, en cuanto al consumo de<br />
opioides durante la internación.<br />
Materiales y métodos: Se recolectaron en forma retrospectiva los datos prospectivos de las historias clínicas de pacientes<br />
con una instrumentación con tornillos transpediculares percutáneos operados entre Junio del 2016 y Diciembre del 2018. 32<br />
pacientes cumplieron con los criterios de selección. Se infiltró en el momento del cierre quirúrgico con una solución preparada<br />
con 150 mg de ropivacaína, 0,7 mcg/kg de dexmedetomidina y 60 mg de ketorolac, disuelto en solución fisiológica estéril para<br />
completar 40ml (Grupo M) y se la comparó con pacientes en los cuales solo se infiltró con 150mg de ropivacaína (Grupo E).<br />
Resultados: El consumo de equivalentes de morfina durante las primeras 72hs postoperatorias presentó en el grupo M una<br />
mediana de 0mg, y el grupo E, una mediana de 9,5mg (RIQ de 13,35), con una p&lt;0,000. Por el contrario el consumo de<br />
morfina en la sala de recuperación presentó una mediana de 0mg (RIQ de 2) para el grupo M, y de 2mg (RIQ de 5) para el<br />
grupo E, sin encontrarse una diferencia significativa, p=0,132.<br />
Conclusión: Los resultados obtenidos en la comparación del consumo de opioides durante las primeras 72hs de la<br />
internación permite inferir que esta combinación de fármacos es superior respecto a la infiltración estándar con ropivacaína,<br />
independientemente de la estrategia analgésica utilizada durante el tiempo quirúrgico.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Objectives: To assess the effectiveness of a surgical site infiltration with ropivacaine, dexmedetomidine and ketorolac,<br />
in reducing opioid consumption in patients with a transpedicular dorsolumbar instrumentation using a minimally invasive<br />
technique.<br />
Materials y methods: We retrospectively collected data from patient’s charts from June of 2016 to December of 2018. 32<br />
patients with minimally invasive transpedicular dorsolumbar instrumentation, who met all criteria, were included in the analysis.<br />
During wound closure a mixture of 150mg of ropivacaine, 0,7mcg/kg of dexmedetomidine and 60mg of ketorolac, diluted in<br />
normal saline to achieve 40ml was injected (Group M). We compared them with patients in whom only 150mg of ropivacaine<br />
and saline where injected in the surgical site (Group E).<br />
Results: Morphine equivalents use during the first 72 hours postoperative had a median of 0mg for group M, and of 9,5mg (IQR<br />
of 13.35), with a p&lt;0,000. On the contrary, morphine use during post anesthesia care unit stance had a median of 0mg (IQR of<br />
2) for group M and of 2mg (IQR of 5) for group E, without a statistically significant difference, p=0,132.<br />
Conclusion: The result of the analysis of opioid consumption during the first 72 hours postoperative allows concluding that<br />
the infiltration of these 3 drugs together its superior to the standard infiltration with ropivacaine, independently of the analgesic<br />
strategy used during the surgery]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Sebastián Kornfeld]]></dcterms:creator>
    <dcterms:creator><![CDATA[Hernan Bovery]]></dcterms:creator>
    <dcterms:creator><![CDATA[Jorge Rasmussen]]></dcterms:creator>
    <dcterms:creator><![CDATA[Federico Landriel]]></dcterms:creator>
    <dcterms:creator><![CDATA[Santiago Hem]]></dcterms:creator>
    <dcterms:creator><![CDATA[ Claudio Yampolsky]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Diciembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Agosto 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Agosto 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
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28. Perkins FM KH. Chronic Pain as an Outcome of Surgery A Review<br />
of Predictive Factors. Anesthesiology 2000; 93(4): 1123–33.<br />
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SJ, et al. Morbidity and mortality of major adult spinal surgery. A<br />
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2012; 12(1): 22–34.<br />
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Pharmacokinetics of Dexmedetomidine. Anesth Analg<br />
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lumbar fusion. Br. J. Neurosurg. 2017; 31(2): 167–71.<br />
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Miyawaki T. Dexmedetomidine enhances the local anesthetic action<br />
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96–101.<br />
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ropivacaine and levobupivacaine. Curr. Opin. Anaesthesiol. 2008;<br />
21(5): 645–50.]]></dcterms:references>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1287">
    <dcterms:title><![CDATA[Experiencia con la “técnica de Xiao” para reinervación<br />
de la vejiga, en pacientes con mielomeningocele y vejiga<br />
neurogénica, 8 años de seguimiento, en adultos<br />
Premio Senior. XV Jornadas Argentinas de Neurocirugía de AANC]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Trabajos Premiados]]></dcterms:description>
    <dcterms:abstract><![CDATA[Objetivo: Restaurar función de vaciado vesical en pacientes con vejiga neurogénica por medio de la reinervación de la vejiga a<br />
través de la creación de reflejo sómato-visceral. Registrar complicaciones neuroquirúrgicas, urológicas y ortopédicas.<br />
Evaluar dificultades técnico-quirúrgicas y los resultados de 5 casos realizados en Argentina.<br />
Introducción: La vejiga neurogénica es una complicación secundaria al daño neurológico en los pacientes con<br />
mielomeningocele (MMC). Para lograr vaciar la vejiga deben realizar cateterismo intermitente. La técnica Xiao se basa en<br />
permitir la generación de un arco reflejo somato visceral por medio de una anastomosis entre una raíz eferente donante y la<br />
raíz motora S2 S3 que permita el vaciado vesical sin cateterismo.<br />
Material y métodos: Por medio de un estudio descriptivo retrospectivo, se analizan los<br />
resultados obtenidos luego de realizar la técnica Xiao, en el año 2010, en 5 pacientes con MMC y vejiga neurogénica. Los<br />
pacientes fueron operados en el Instituto de Rehabilitación (IREP). Fueron evaluados en forma multidisciplinaria tanto pre<br />
como en el postoperatorio por neurocirujanos, neurólogos, urólogos, clínicos y kinesiólogos.<br />
Resultados: Los pacientes que presentaron mejores resultados fueron los más jóvenes y los que no presentaban daño<br />
estructural de la vejiga al momento de la cirugía, lo que coincide con los resultados compartidos por los demás centros donde<br />
fue realizada esta técnica.<br />
Conclusiones: La técnica de Xiao puede considerarse una opción para el tratamiento de la vejiga neurogénica. Aunque nuestra<br />
serie es muy pequeña para dar conclusiones, los resultados globales de todas las series muestran resultados alentadores.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Objective: To restore bladder function in patients with neurogenic bladder through the reinnervation through restauration<br />
of somatic-visceral reflex. Record neurosurgical, urological and orthopedic complications. To evaluate technical-surgical<br />
difficulties and the results of 5 cases performed in Argentina.<br />
Introduction: Neurogenic bladder is a complication secondary to neurological damage in patients with myelomeningocele<br />
(MMC). To achieve emptying of the bladder, intermittent catheterization must be performed. The “Xiao technique” is based on<br />
allowing the generation of a visceral somatic-reflex arc by means of an anastomosis between a donor efferent root and the<br />
motor root S2-S3 that allows bladder emptying without catheterization.<br />
Material and methods: Through a retrospective descriptive study, the results obtained after performing the “Xiao technique”<br />
in 5 patients with MMC and neurogenic bladder were analyzed. The patients were operated at the Rehabilitation Institute<br />
(IREP). They were evaluated with a multidisciplinary team, both pre and post-surgery. The team was formed by neurosurgeons,<br />
neurologists, urologists, clinicians and kinesiologists.<br />
Results: The patients who presented the best results were the youngest and those who did not present structural damage of<br />
the bladder at the time of surgery, which match the results shared by the other centers where this technique was performed.<br />
Conclusions: “Xiao&#039;s technique” can be considered an option for the treatment of neurogenic bladder. Although our series is<br />
too small to make conclusions, the overall results of all the series show encouraging results.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Beatriz Mantese]]></dcterms:creator>
    <dcterms:creator><![CDATA[ Romina Argañaraz]]></dcterms:creator>
    <dcterms:creator><![CDATA[Enrique Turina]]></dcterms:creator>
    <dcterms:creator><![CDATA[Cristian Sager]]></dcterms:creator>
    <dcterms:creator><![CDATA[Martin Segura]]></dcterms:creator>
    <dcterms:creator><![CDATA[Fernando Ford]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Diciembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Agosto 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Agosto 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:references><![CDATA[1. Amarenco G, Sheikh Ismaël S, Chesnel C, Charlanes A, LE Breton<br />
F. Diagnosis and clinical evaluation of neurogenic bladder. Eur J<br />
Phys Rehabil Med. 2017 Dec;53(6):975- 980.<br />
2. Bodner DR. How electrical stimulatio improves micturion.<br />
Contemporary Urol 1990;3:39- 45.<br />
3. Borgstedt-Bakke JH, Fenger-Grøn M, Rasmussen MM. Correlation<br />
of mortality with lesion level in patients with myelomeningocele: a<br />
population-based study. J Neurosurg Pediatr. 2017 Feb;19(2):227-<br />
231.<br />
4. Brindley G S, Polkey C E, Rushton D N. Sacral anterior root<br />
stimulator for bladder control in paraplegia: the first 50 cases. J<br />
Neurol Neurosurg Psychiatry.1986;49: 1004–1011.<br />
5. Carr MC. Neuropathic bladder in the neonate. Clin Perinatol. 2014<br />
Sep;41(3):725-33.<br />
6. Hald T, Agrawal G, Kantrowitz A. Studies in stimulation of the<br />
bladder and its motor nerves. Surg. 1966;60:848-56.<br />
7. Hold T, Agrawal G, Kantrowitz A. Studies in stimulation of the<br />
bladder and its motor nerves. Surg. 1966;60: 848–853.<br />
8. Jonas U, Henie JP, Tanagho EA. Studies on the feasibility of urinary<br />
bladder evacuation by direct spinal cord stimulation. Parameters of<br />
must effective stimulation. Invest Urol 1975;13:142-5.<br />
9. Kenneth Peters, Feber KM, Bennett RC. Sacral versus pudendal<br />
nerve stimulation for voiding dysfunction: a prospective, singleblinded,<br />
randomized, crossover trial. Neurourol Urodyn.<br />
2005;24(7):643-7.<br />
10. Kenneth Peters, Holly Gilmer, Kevin Feber. Us Pilot study of<br />
Lumbar to Sacral Nerve Rerouting to Restore Voiding and Bowel<br />
Function in Spina Bifida. Adv Urol. 2014;2014:863209.<br />
11. Vorstam B, Schlossberg S M, Kass L, Devince J. Urinary bladder<br />
reinnervation. J Urol.1986;136: 964–969.<br />
12. Vorstam B, Schlossberg S M, Kass L. Investigation on urinary<br />
bladder reinnervation: historical perspective and review. Urol.<br />
1987;30: 89–96.<br />
13. Xiao CG, de Groat WC, Godec CJ, Dai C, Xiao Q. “Skin-CNSbladder”<br />
reflex pathway for micturition after spinal cord injury and<br />
its underlying mechanisms. J Urol 1999;162:936- 42.<br />
14. Xiao CG, et al. An artificial somatic-autonomic reflex pathway<br />
procedure for bladder control in children with spina bifida. J Urol<br />
2005; 173:2112-6.<br />
15. Xiao CG, Schlossberg SM, Morgan CW, Kodama R. A posible new<br />
reflex pathway for micturition after spinal cord injury. J urol 1990;<br />
143:356.<br />
16. Xiao, CG., Du, M.-X., Dai, C., Li, B., Nitti, V.W. and de Groat,<br />
W. C.: An artifcial somatic- central nerous system-autonomic<br />
reflex pathway for controllable micturion after spinal cord injury:<br />
preliminary results in 15 patients. J Urol. 2003; 170: 1237.]]></dcterms:references>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1286">
    <dcterms:title><![CDATA[Parte I: Anatomía microquirúrgica tridimensional de la ínsula]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Artículo Original]]></dcterms:description>
    <dcterms:abstract><![CDATA[Introducción: El lóbulo de la ínsula, o ínsula, se encuentra oculto en la superficie lateral del cerebro. La ínsula está localizada<br />
profundamente en el surco lateral o cisura silviana, recubierta por los opérculos frontal, parietal y temporal.<br />
Objetivo: Estudiar la compleja anatomía del lóbulo de la ínsula, una de las regiones de mayor complejidad quirúrgica del<br />
cerebro humano, y su correlación anatómica con casos quirúrgicos.<br />
Material y Métodos: En la primera parte de este estudio presentamos los resultados de nuestras disecciones microquirúrgicas<br />
en fotografías 2 D y 3D; en la segunda parte de nuestro trabajo, la correlación anatómica con una serie de 44 cirugías en<br />
pacientes con tumores de la ínsula, principalmente gliomas, operados entre 2007 y 2014.<br />
Resultados: Extenso conjunto de fibras subcorticales, incluyendo el fascículo uncinado, fronto-occipital inferior y el fascículo<br />
arcuato, conectan la ínsula a las regiones vecinas. Varias estructuras anatómicas responsables por déficits neurológicos<br />
severos están íntimamente relacionadas con la cirugía de la ínsula, tales como lesiones de la arteria cerebral media, cápsula<br />
interna, áreas del lenguaje en el hemisferio dominante y arterias lenticuloestriadas.<br />
Conclusión: El entrenamiento en laboratorio de neuroanatomía, estudio de material impreso en 3D, el conocimiento sobre<br />
neurofisiología intra-operatoria y el uso de armamento neuroquirúrgico moderno son factores que influencian en los resultados<br />
quirúrgicos.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Introduction: The insular lobe, or insula, is the cerebral lobe sitting deep in the sylvian fissure and hidden by the lateral surface<br />
of the brain. It is covered by the frontal, parietal and temporal operculum.<br />
Objectives: To study the anatomy of the insular lobe, one of the most complex parts of the human brain, and to correlate this<br />
anatomy with intraoperative findings.<br />
Materials and Methods: In the first part of this article we show the results of our dissections, documented in 2D and 3D, and<br />
focus on microsurgical anatomy. In the second part we correlate the anatomical structures with intraoperative findings from 44<br />
insular tumor surgeries, mainly gliomas, of patients operated on from 2007 to 2014.<br />
Results: Huge bundles of subcortical fibers, like uncinate, inferior fronto-occipital and arcuate fascicles, connect the insula<br />
to the neighboring structures. Several anatomical structures related to neurological disabilities are closely related to insular<br />
surgery, like the middle cerebral artery, internal capsule, lenticulostriate arteries and cortical and subcortical language circuits.<br />
Conclusions: Microsurgical laboratory training, 3D documentation, knowledge of brain mapping and modern neurosurgical<br />
armamentarium are important factors in achieving good results with insular glioma tumors.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Gustavo Rassier Isolan]]></dcterms:creator>
    <dcterms:creator><![CDATA[Alvaro Campero]]></dcterms:creator>
    <dcterms:creator><![CDATA[Pablo Ajler]]></dcterms:creator>
    <dcterms:creator><![CDATA[Edgar Manuel Garcete Farina]]></dcterms:creator>
    <dcterms:creator><![CDATA[Thomas M Frigeri]]></dcterms:creator>
    <dcterms:creator><![CDATA[Leandro Infantini Dini]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Diciembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Octubre 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Junio 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
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    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1285">
    <dcterms:title><![CDATA[Volumen 33 Número 4]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1284">
    <dcterms:title><![CDATA[Utilización de las zonas de entrada seguras para el abordaje<br />
de lesiones intrínsecas de tronco cerebral en adultos]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Artículo Original]]></dcterms:description>
    <dcterms:abstract><![CDATA[Introducción: Las “zonas de entrada seguras” (ZES) al tronco cerebral describen accesos destinados a preservar estructuras<br />
críticas. La mayoría de las publicaciones son descripciones anatómicas; existiendo pocas sobre su aplicación. En este<br />
escenario, nuestro trabajo puede sumar información para el manejo quirúrgico en casos seleccionados.<br />
Material y Métodos: De una serie de 13 pacientes, se presentan 9 que no eran candidatos para biopsia estereotáctica y<br />
recibieron microcirugía. Las localizaciones fueron: mesencéfalo (3), tectum (1), protuberancia (2) y bulbo (3). Cinco pacientes<br />
tuvieron KPS =&gt; 70; y 4, KPS &lt;70. Diferentes ZES fueron utilizadas según la topografía lesional. El grado de resección se basó<br />
en la biopsia intraoperatoria y el monitoreo neurofisiológico.<br />
Resultados: Los hallazgos patológicos fueron: astrocitoma pilocítico (1), glioma de bajo grado (1), hemangioblastoma (1),<br />
subependimoma (1), disgerminoma (1), y lesiones pseudotumorales (3 cavernomas y 1 pseudotumor inflamatorio). El grado de<br />
resección fue completo (4), subtotal (3), y biopsia fue considerada suficiente en (2). Un paciente falleció en el postoperatorio.<br />
Discusión: Las lesiones del tronco cerebral son infrecuentes en adultos. Las controversias surgen cuando se balancean los<br />
beneficios de obtener diagnóstico histopatológico y los riesgos potenciales de procedimientos invasivos. La amplia variedad<br />
de hallazgos en esta localización exige una precisa definición histopatológica, que no solamente determinará la terapéutica<br />
adecuada, sino que advierte sobre las consecuencias potencialmente catastróficas de los tratamientos empíricos. Las ZES<br />
ofrecen un acceso posible y seguro, aunque es más realista considerarlas como áreas para abordar lesiones intrínsecas con<br />
baja morbilidad más que como zonas completamente seguras.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Introduction: The “safe entry zones” (SEZ) to the brainstem are special entrances described to preserve critical structures.<br />
Most publications correspond to anatomic research; few papers report their application in surgery. In this scenario, our report<br />
could add information to the surgical management in selected cases.<br />
Material and Methods: Out of a series of 13 patients, 9 were non-candidates for stereotactic biopsy and received<br />
microsurgery. Localizations of the lesions were: mesencephalus (3), tectal plate (1), pons (2) and medulla oblongata (3). Five<br />
patients had KPS =&gt; 70; 4, KPS &lt;70. Different SEZ were used according to lesional topography. The extent of resection were<br />
based on the frozen pathology findings and neurophysiological monitoring.<br />
Results: A variety of pathological findings were found: low-grade glioma (1); pilocytic astrocytoma (1); hemangioblastoma<br />
(1); subependimoma (1); disgerminoma (1); pseudotumoral lesions (cavernomas 3 and inflammatory pseudotumor 1). The<br />
extent of resection was complete (4), subtotal (3), and biopsy was considered sufficient in 2 cases. One patient died 96-hourspostoperative<br />
due to brainstem edema.<br />
Discussion: Brainstem structural lesions are uncommon in adults. Controversies arise regarding the need of histologic<br />
diagnosis, weighing benefits of a reliable diagnosis and the potential disadvantages of the invasive procedures. The accurate<br />
histopathological definition could not only determine an adequate therapy, but also can prevent the disastrous consequences<br />
of empiric treatments. The SEZ provides a feasible and safe access, although it is more realistic to consider them as areas to<br />
approach intrinsec lesions with less morbidity than to consider them as completely safe entrances.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Alejandra T. Rabadán]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Diciembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Agosto 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Julio 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
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8. Kyoshima K, Sakai K, Goto T, Tanabe A, Sato A, Nagashima H,<br />
Nakayama J. Gross total surgical removal of malignant glioma from<br />
the medulla oblongata: report of two adult cases with reference to<br />
surgical anatomy. Journal of Clinical Neuroscience 2004; 11:1, 75-80.<br />
9. Massager N, Davi P, Goldman S. Combined magnetic resonance<br />
imaging and positron emission tomography-guided stereotactic<br />
biopsy in brainstem mass lesions: diagnostic yield in a series of 30<br />
patients. J Neurosurg 2000; 93: 951-957.<br />
10. Morota N, Deletis V. The importance of brainstem mapping<br />
in brainstem surgical anatomy before the fourth ventricle and<br />
implication for intraoperative neurophysiological mapping. Acta<br />
Neurochir (Wien) 2006; 148: 499-509.<br />
11. Mursch K, Halatsch ME, Markakis E et al. Intrinsec brain stem<br />
tumors in adults: results of microneurosurgical treatment of 16<br />
consecutive patients. Br J Neurosurg 2005; 19 (2): 128-36.<br />
12. Rabadán AT, Campero A, Hernández D. Surgical application of the<br />
suboccipital subtonsillar approach to reach the inferior half of medulla<br />
oblongata tumors in adult patients. Front Surg. 2016 13, 2: 72.<br />
13. Rabadán AT, Hernández D. Importancia del diagnóstico<br />
histopatológico en el tratamiento de las lesiones del tronco cerebral<br />
en adultos. MEDICINA (Buenos Aires) 2018; 78: 305-310.<br />
14. Rachinger W, Grau S, Holtmannspotter M, Herms J, Tonn JC,<br />
Kreth FW. Serial stereotactic biopsy of brainstem lesions in adults<br />
impacting diagnostic accuracy compared with MRI only. J Neurol<br />
Neurosurg Psychiatry 2009; 80: 1134-9.<br />
15. Recalde R, Figueiredo EG, de Oliveira E. Microsurgical anatomy of<br />
the safe entry zones on the anterolateral brainstem related to surgical<br />
approaches to cavernous malformations. Neurosurgery 2008;<br />
62:509-517.<br />
16. Rhoton A. The Rothon’s Collection. http://www.rothon.ineurodb.org.<br />
17. Sala F. A spotlight on intraoperative neurophysiological monitoring<br />
of the lower brainstem. Clinical Neurophysiology 2017; 128 (2017)<br />
1369–1371 .<br />
18. Salmaggi A, Fariselli L, Milanesi I, Lamperti E, Silvani A, Bizzi<br />
A, et al. Natural history and management of brainstem gliomas in<br />
adults. A retrospective Italian study. J Neurol 2008; 255: 171-177.<br />
19. Schumacher M, Schulte-Monting J, Stoeter P, Warmuth-Metz<br />
M, Solymosi L (2007) Magnetic resonance imaging compared<br />
with biopsy in the diagnosis of brainstem diseases of childhood: a<br />
multicenter review. J Neurosurg 106: 111-119.<br />
20. Ziyal IM, Sehkar LN, Salas E, Subtonsillar-transcerebellomedullary<br />
approach to lesions involving the fourth ventricle, the<br />
cerebellomedullary fissure and the lateral brainstem. Br J Neurosurg<br />
1999 Jun;13(3):276-84.]]></dcterms:references>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1283">
    <dcterms:title><![CDATA[Clasificación del tubérculo suprameatal y análisis<br />
morfométrico con enfoque quirúrgico del hueso temporal]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Artículo Original]]></dcterms:description>
    <dcterms:abstract><![CDATA[Introducción: El hueso temporal es una estructura valiosa en el abordaje de patologías intracraneales a la fosa media y posterior,<br />
requiriendo en ocasiones la realización de petrosectomías anteriores, posteriores o abordajes combinados para la resección de<br />
tumores en dichas regiones. El propósito del presente estudio es realizar análisis morfométrico con enfoque quirúrgico del hueso<br />
temporal, en cráneos adultos, con énfasis en el tubérculo suprameatal (TSM) teniendo en consideración sus relaciones anatómicas.<br />
Material y métodos: El presente estudio se realizó en las instalaciones de la Facultad de Medicina de la Universidad Nacional<br />
Autónoma de México (UNAM). Se analizaron 200 huesos temporales de 100 cráneos humanos adultos. Se dio énfasis al TSM de<br />
acuerdo a su ubicación y tamaño, clasificándolo en: anterior medio o posterior y en tipo I (0-1 mm), tipo II (2-3 mm) y tipo III (&gt;3 mm).<br />
Además, se realizaron mediciones con enfoque quirúrgico de la porción petrosa del hueso temporal y de la cresta supramastoidea.<br />
Resultados: El TSM se observó en 171 especímenes estudiados (85.5%). Entre ellos, la posición posterior fue la más frecuente<br />
85 de 171 (49.70%), seguida de la posición media 43 (25.14%) y por último la posición anterior 43 (25.14%). En cuanto al<br />
tamaño, se encontró con mayor frecuencia el tipo II en 99 de los especímenes (49.5%), el tipo I en 82 especímenes (41%)<br />
y tipo III en 19 (9.5%). El asterion se reflejó dentro de la impresión de los senos en la mayoría 48.5%, la unión de la cresta<br />
supramastoidea con sutura escamosa se reflejaba en 98.5% de los casos a la fosa media.<br />
Discusión: En nuestra búsqueda de información no se cuenta con datos para realizar comparación con la obtenida en<br />
este estudio del tubérculo suprameatal, el hallazgo encontrado parece indicar que se encuentra una relación directa con la<br />
presencia de la impresión del surco del seno petroso superior. La distribución de acuerdo a su posición reviste importancia<br />
cuando se encuentra en grado III puesto que plantea una dificultad técnica, en abordajes como en petrosectomías, o bien, al<br />
cavum de Meckel desde un abordaje retrosigmoideo.<br />
Conclusión: La observación anatómica y clasificación que realizamos del tubérculo suprameatal, una estructura muy poco<br />
evaluada, nos da una consideración preoperatoria y transoperatoria cuando realizamos abordaje que involucra la cara<br />
posterior de la porción petrosa del hueso temporal]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Introduction: The temporal bone is a valuable structure in the approach of intracranial pathologies to the middle and posterior<br />
fossa. Sometimes requiring the performance of petrosectomies or combined approaches for the resection of tumors in these<br />
regions. The purpose of this study is to perform morphometric analysis in adult skulls with a surgical approach to the temporal<br />
bone, with emphasis on the suprameatal tubercle (SMT) taking into account their anatomical relationships.<br />
Material and methods: The present study was carried out in the facilities of the Faculty of Medicine of the National Autonomous<br />
University of Mexico (UNAM). 200 temporal bones from 100 adult human skulls were analyzed. The SMT was emphasized according to<br />
its location and size, classifying it as: anterior, middle, or posterior and type I (0-1 mm), type II (2-3 mm) and type III (&gt; 3mm). In addition,<br />
measurements were made with a surgical approach of the petrosal portion of the temporal bone and the supramastoid crest.<br />
Results: The SMT was observed in 171 specimens studied (85.5%). Among them, the posterior position was the most frequent<br />
85 of 171 (49.70%), followed by the middle position in 43 (25.14%) and finally the anterior position in 43 (25.14%). In terms of<br />
size, type II was more frequently found in 99 of the specimens (49.5%), type I in 82 specimens (41%) and type III were found in<br />
19 (9.5%). The asterion was reflected within the impression of the sinuses in the majority 48.5%, the union of the supramastoid<br />
crest with squamous suture was reflected in 98.5% of the cases to the middle fossa.<br />
Discussion: In our search for information, there is no data to make a comparison with that obtained in this study of the<br />
suprameatal tubercle. The findings seems to indicate that there is a direct relationship with the presence of the impression of<br />
the groove of the upper petrosal sinus. The distribution according to its position is important when it is in grade III since it poses<br />
a technical difficulty, in approaches such as petrosectomies, or approach to Meckel’s cave from a retrosigmoid approach.<br />
Conclusion: The anatomical observation and classification that we perform of the suprameatal tubercle, a very poorly evaluated<br />
structure, gives us a preoperative and transoperative consideration when we perform an approach that involves the posterior<br />
aspect of the petrosal portion of the temporal bone.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Humberto Reyna Méndez]]></dcterms:creator>
    <dcterms:creator><![CDATA[Enrique López Berumen]]></dcterms:creator>
    <dcterms:creator><![CDATA[ José Alfredo Espinosa Mora]]></dcterms:creator>
    <dcterms:creator><![CDATA[Alberto Manuel Angeles Castellanos]]></dcterms:creator>
    <dcterms:creator><![CDATA[Laura Matilde Ubaldo Reyes]]></dcterms:creator>
    <dcterms:creator><![CDATA[Ignacio Mora Magaña]]></dcterms:creator>
    <dcterms:creator><![CDATA[Diego Méndez Rosito]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Diciembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Septiembre 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Julio 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:references><![CDATA[BIBLIOGRAFÍA<br />
1. Blaser SI, Padfield N, Chitayat D, Forrest CR. Skull base<br />
development and craniosynostosis. 2015;45. doi:10.1007/s00247-<br />
015-3320-1.<br />
2. Bayraktar B, Polat G, Gurel I. Surgical Anatomy of the Temporal<br />
Bone and Measurements of the Skull Base for Transpetrosal<br />
Approaches. 1998;75(1):33-39.<br />
3. Rhoton AL. The Temporal Bone and Transtemporal Approaches.<br />
2000;47(3).<br />
4. Muren C. THE INTERNAL ACOUSTIC MEATUS Anatomic<br />
variations and relations to other temporal bone structures.<br />
1986;27(January):505-512.<br />
5. Peris-celda M, Perry A, Carlstrom P, Graffeo CS. Intraoperative<br />
Management of an Enlarged Suprameatal Tubercle During<br />
Microvascular Decompression of the Trigeminal Nerve , Surgical<br />
and Anatomical Description : 2-Dimensional. 2019;0(0):2019.<br />
doi:10.1093/ons/opz027.<br />
6. Day, J. Diaz, M.D.; Kellogg, Jordi X. MS., Fukushima, Takanori,<br />
M.D., D.M.Sc.; Giannotta, Steven L. MD, Department.<br />
Microsurgical Anatomy of the Inner Surface of the Petrous Bone:<br />
Neuroradiological and Morphometric Analysis as an Adjunct to<br />
the Retrosigmoid Transmeatal Approach Surgical Anatomy and<br />
Technique AUTHOR(S): 1994;34(6).<br />
BIBLIOGRAFÍA<br />
1. Seclen D, Salas E,Nuñez M, Mural M .Región petroclival. En: Campero A, Ajler P ed.Neuroanatomía Quirúrgica. Buenos Aires, Editorial<br />
Journal; 2019, 215-225.<br />
7. Adams Pérez J, Rassier Isolan G, Pires De Aguiar PH, Antunes AM.<br />
Volumetry and analysis of anatomical variants of the anterior portion<br />
of the petrous apex outlined by the Kawase triangle using computed<br />
tomography. J Neurol Surgery, Part B Skull Base. 2014;75(3):147-<br />
151. doi:10.1055/s-0033-1356491<br />
8. Fournier H-D, Mercier P, Roche P-H. Surgical anatomy<br />
of the petrous apex and petroclival region. 2008;32:91-146.<br />
doi:10.1007/978-3-211-47423-5_5.<br />
9. Altieri R, Sameshima T, Pacca P, et al. Detailed anatomy knowledge :<br />
first step to approach petroclival meningiomas through the petrous<br />
apex . Anatomy lab experience and surgical series. Neurosurg Rev.<br />
2016. doi:10.1007/s10143-016-0754-3.<br />
10. Peris-Celda M, Perry A, Carlstrom LP, Graffeo CS, Driscoll<br />
CLW, Link MJ. Key anatomical landmarks for middle fossa<br />
surgery: a surgical anatomy study. J Neurosurg. 2018:1-10.<br />
doi:10.3171/2018.5.jns1841.<br />
11. R. Chopra, N. Fergie, D. Mehta LL. The middle cranial fossa<br />
approach : an anatomical study. Surg Radiol Anat. 2003;(2002):348-<br />
351. doi:10.1007/s00276-002-0076-8.<br />
12. Pareschi R, Danesi G, Stefini R, Bivona R, Valera CI. The<br />
Transpetrosal Approaches System in Posterior Fossa Meningiomas<br />
Surgery : Rationale and Results. 2019.]]></dcterms:references>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1282">
    <dcterms:title><![CDATA[Cavernomas múltiples: abordaje microquirúrgico al área peritrigeminal y endoscópico transtentorial <br />
al área temporomesial<br />
Premio Video. XV Jornadas de Neurocirugía 2019]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Video]]></dcterms:description>
    <dcterms:abstract><![CDATA[Introducción: Los cavernomas cerebrales de localización en el tronco encefálico representan un desafío dentro de la neurocirugía por la nobleza de esta estructura. A su vez, el sangrado en esta localización se relaciona con elevada morbilidad y mortalidad. El síndrome de cavernomatosis múltiple familiar es un trastorno autosómico dominante que se caracteriza por la presencia de 5 o más cavernomas cerebrales en 2 o más miembros de una familia. El tratamiento quirúrgico de esta enfermedad se limita a aquellos cavernomas sintomáticos. Objetivo: Presentar la exéresis múltiple de tres cavernomas ipsilaterales supra e infratentoriales mediante técnica combinada microquirúrgica y endoscópica.<br />
Materiales y métodos: Paciente femenina de 49 años que presenta hematoma protuberancial con hemiparesia izquierda. Tiene antecedentes de cavernomas cerebrales en familiares de primer grado. En Resonancia Magnética con secuencias de susceptibilidad magnética (SWI) se evidencian malformaciones cavernosas múltiples en protuberancia, cerebelo, región temporomesial derecha y lóbulo frontal derecho. Se plantea la exéresis microquirúrgica de la lesión protuberancial y cerebelosa combinado con resección transtentorial endoscópica del cavernoma temporomesial.<br />
Resultados: Mediante abordaje supracerebeloso infratentorial se logró la exéresis del cavernoma cerebeloso y protuberacial. Se utilizó el área peritrigeminal derecha como área de acceso seguro al tronco. Con el uso de endoscopio rígido se realizó apertura del tentorio a nivel del conducto auditivo interno con posterior resección endoscópica del cavernoma temporomesial. La paciente curso el postoperatorio sin secuelas neurológicas.<br />
Conclusión: La precisión del microscopio y la versatilidad del endoscopio nos permiten realizar resecciones de múltiples lesiones en distintas áreas.<br />
<br />
]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Background: Brain stem cavernous malformations represent a challenge for neurosurgeons due to the strong functionality role of this anatomic structure. At the same time, the bleeding in this area is associated with high morbidity and mortality. Familial multiple cavernomatosis syndrome is an autosomal dominant disorder defined as the presence of five or more brain cavernous malformation in two or more members of a family. In this disease, the surgical treatment is limited to the symptomatic cavernomas.<br />
Objective: Present the surgical treatment of three ipsilateral cavernomas using a combined microsurgical and endoscopic technique. Methods: 49-years-old female patient attended to the emergency department with acute left hemiparesis and a pons bleeding. She had family history of cerebral cavernous malformation. Magnetic resonance with susceptibility weight imaging (SWI) shows multiple cavernous malformation in pons, cerebellum, right parahippocampal region and right frontal lobe. The surgical planning consisted of microsurgical excision of the cerebellar and pons lesions combined with a transtentorial endoscopic approach to the right parahippocampal cavernoma. <br />
Results: We made a supracerebellar and infratentorial approach with satisfactory excision of cerebellar and pons cavernomas. We use the peritrigeminal zone as a safety entry to the pons. With a rigid skull base endoscope, we opened the tentorium just above the internal auditory meatus. Also, we achieved an endoscopic exeresis of the parahippocampal cavernoma. The patient did not have neurological deficits after surgery.<br />
Conclusion: The precision of the microscope and the versatility of the endoscope let us attempt excision of multiple lesions in distant areas.<br />
<br />
]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Franco Rubino]]></dcterms:creator>
    <dcterms:creator><![CDATA[Juan Iaconis Campbell]]></dcterms:creator>
    <dcterms:creator><![CDATA[German Degano]]></dcterms:creator>
    <dcterms:creator><![CDATA[Miguel Mural]]></dcterms:creator>
    <dcterms:creator><![CDATA[Maximiliano Núñez]]></dcterms:creator>
    <dcterms:creator><![CDATA[Eduardo Salas]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Diciembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Agosto 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Agosto 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1281">
    <dcterms:title><![CDATA[Drenaje ventricular al exterior de tunelización larga: un<br />
método costo-efectivo para reducir las complicaciones<br />
Premio Beca Asociación Argentina de Neurocirugía. XV Jornadas Argentinas<br />
de Neurocirugía 2019]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Artículo Original]]></dcterms:description>
    <dcterms:abstract><![CDATA[Introducción: La colocación de drenajes ventriculares al exterior (DVE) es uno de los procedimientos más frecuentes de<br />
la neurocirugía, tanto en pediatría como en adultos, sin embargo, no se encuentra exento de complicaciones. La tasa de<br />
infección asociada al drenaje puede serdel 25%. En nuestro Hospital encontramos una incidencia del 22% anual.<br />
Al ser sistemas que no cuentan con una regulación de la salida del líquido, el paciente debe permanecer en decúbito dorsal<br />
estricto todo el tratamiento.<br />
Nuestro objetivo es diseñar un nuevo sistema de drenaje ventricular al exterior de tunelización larga (DVET) que lidie con estos<br />
problemas al mismo tiempo que reduzca los costos hospitalarios.<br />
Material y métodos: Se realizó un ensayo clínico prospectivo en el que se colocaron 25 DVETL entre el 1/9/2018 al 1/5/2019<br />
que se compararon con el sistema tradicional de DVE.<br />
Resultados: La presencia de fístula se asoció más frecuentemente a los DVE en comparación con los DVETL, esta diferencia<br />
fue estadísticamente significativa (30% vs 8% p=0,029). La presencia de infección asociada al drenaje fue significativamente<br />
mayor en los DVE en comparación con los DVETL, esta diferencia fue estadísticamente significativa (22% vs 0% p=0,009). Los<br />
pacientes con DVE tradicional utilizaron el doble de recursos y generaron el doble de costos que los pacientes con DVETL.<br />
Conclusión: Se realizó una presentación detallada del nuevo sistema de DVETL que presenta una disminución en la incidencia<br />
de fístula de LCR e infección asociada al drenaje. A su vez aparenta ser costo-efectiva en comparación con el sistema<br />
tradicional de DVE.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Introduction: External ventricular drain (EVD) placement is one of the most frequent procedures in neurosurgery, both in<br />
pediatrics and in adults. The global rate of ventriculostomy-associated infections could rich 25%. In our Hospital, we found an<br />
annual incidence of 22%.<br />
In addition, since it does not have a regulation of cerebral spinal fluid (CSF) flow, the patient must remain in strict dorsal<br />
decubitus throughout the entire treatment.<br />
Our goal is to design a new long-tunneled external ventricular drain (LTEVD) that deals with these problems while reducing<br />
hospital costs.<br />
Material and method: A prospective clinical trial was conducted in which 25 LTEVD were placed between 1/9/2018 and<br />
1/5/2019 that were compared with the traditional EVD system.<br />
Results: The presence of CSF fistula was associated more frequently with EVD compared to LTEVD; this difference was<br />
statistically significant (30% vs. 8% p = 0.029). The presence of associated infection was significantly higher in EVD compared<br />
to LTEVD, and this difference was statistically significant (22% vs. 0% p = 0.009). Patients with traditional EVD used twice as<br />
many resources and generated twice the cost as patients with DVETL.<br />
Conclusion: A detailed presentation was made of the new LTEVD system that presents a decrease in the incidence of CSF<br />
fistula and associated infection. At the same time, it appears to be cost-effective in comparison with the traditional DVE system.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Amparo Sáenz]]></dcterms:creator>
    <dcterms:creator><![CDATA[Romina Argañaraz]]></dcterms:creator>
    <dcterms:creator><![CDATA[Beatriz Mantese]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Diciembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Agosto 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Agosto 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:references><![CDATA[1. Arabi Y, Memish ZA, Balkhy HH, et al. Ventriculostomy-associated<br />
infections: Incidence and risk factors. Am J Infect Control.<br />
2005;33(3):137-143. doi:10.1016/j.ajic.2004.11.008.<br />
2. Attenello FJ, Garces-Ambrossi GL, Zaidi HA, Sciubba DM,<br />
Jallo GI. Hospital Costs Associated With Shunt Infections in<br />
Patients Receiving Antibiotic-Impregnated Shunt Catheters<br />
Versus Standard Shunt Catheters. Neurosurg. 2010;66(2):284-289.<br />
doi:10.1227/01.NEU.0000363405.12584.4D.<br />
3. Bota DP, Lefranc F, Vilallobos HR, Brimioulle S, Vincent J-L.<br />
Ventriculostomy-related infections in critically ill patients: a 6-year<br />
experience. J Neurosurg. 2005;103(3):468-472. doi:10.3171/<br />
jns.2005.103.3.0468.<br />
4. Camacho EF, Boszczowski Í, Basso M, et al. Infection rate and risk<br />
factors associated with infections related to external ventricular<br />
drain. Infect. 2011;39(1):47-51. doi:10.1007/s15010-010-0073-5.<br />
5. Cinibulak Z, Aschoff A, Apedjinou A, Kaminsky J, Trost HA,<br />
Krauss JK. Current practice of external ventricular drainage: a survey<br />
among neurosurgical departments in Germany. Acta Neurochir.<br />
2016;158(5):847-853. doi:10.1007/s00701-016-2747-y.<br />
6. Collins CDE, Hartley JC, Chakraborty A, Thompson DNP. Long<br />
subcutaneous tunnelling reduces infection rates in paediatric<br />
external ventricular drains. Childs Nerv Syst. 2014;30(10):1671-<br />
1678. doi:10.1007/s00381-014-2523-3.<br />
7. Edwards NC, Engelhart L, Casamento EMH, McGirt MJ. Costconsequence<br />
analysis of antibiotic-impregnated shunts and external<br />
ventricular drains in hydrocephalus. J Neurosurg. 2015;122(1):139-<br />
147. doi:10.3171/2014.9.JNS131277.<br />
8. González S, Carbonaro M, Fedullo AG, et al. Cerebrospinal<br />
fluid shunt-associated infections in pediatrics: Analysis of the<br />
epidemiology and mortality risk factors. Arch Argent Pediatr.<br />
2018;116(3):198-203. doi:10.5546/aap.2018.eng.198.<br />
9. Hader WJ, Steinbok P. The value of routine cultures of the<br />
cerebrospinal fluid in patients with external ventricular drains.<br />
Neurosurg. 2000;46(5):1149–53–discussion1153–5.<br />
10. Holloway KL, Barnes T, Choi S, et al. Ventriculostomy infections:<br />
the effect of monitoring duration and catheter exchange in<br />
584 patients. J Neurosurg. 1996;85(3):419-424. doi:10.3171/<br />
jns.1996.85.3.0419.<br />
11. Kanik A, Sirin S, Kose E, Eliacik K, Anil M, Helvaci M. Clinical<br />
and economic results of ventriculoperitoneal shunt infections in<br />
children. Turk Neurosurg. 2015;25(1):58-62. doi:10.5137/1019-<br />
5149.JTN.8540-13.2.<br />
12. Khanna RK, Rosenblum ML, Rock JP, Malik GM. Prolonged<br />
external ventricular drainage with percutaneous long-tunnel<br />
ventriculostomies. J Neurosurg. 1995;83:791-794. doi:10.3171/<br />
jns.1995.83.5.0791.<br />
13. Klipin M, Mare I, Hazelhurst S, Kramer B. The process of installing<br />
REDCap, a web based database supporting biomedical research: the<br />
first year. Appl Clin Inform. 2014;5(4):916-929. doi:10.4338/ACI-<br />
2014-06-CR-0054.<br />
14. Korinek AM. Risk factors for neurosurgical site infections after<br />
craniotomy: a prospective multicenter study of 2944 patients. The<br />
French Study Group of Neurosurgical Infections, the SEHP, and the<br />
C-CLIN Paris-Nord. Service Epidémiologie Hygiène et Prévention.<br />
Neurosurg. 1997;41(5):1073–9–discussion1079–81.<br />
15. Lam SK, Srinivasan VM, Luerssen TG, Pan I-W. Cerebrospinal<br />
fluid shunt placement in the pediatric population: a model<br />
of hospitalization cost. Neurosurg Focus. 2014;37(5):E5.<br />
doi:10.3171/2014.8.FOCUS14454.<br />
16. Lewin S, Low SW. External ventricular drain infections; successful<br />
implementation of strategies to reduce infection rate. Singap Med J.<br />
April 2012:1-5.<br />
17. Mayhall CG, Archer NH, Lamb VA, et al. Ventriculostomy-related<br />
infections. A prospective epidemiologic study. N Engl J Med.<br />
1984;310(9):553-559. doi:10.1056/NEJM198403013100903.<br />
18. Meirovitch J, Kitai-Cohen Y, Keren G, Fiendler G, Rubinstein E.<br />
Cerebrospinal fluid shunt infections in children. Pediatr Infect Dis J.<br />
1987;6(10):921-924.<br />
19. Mullan E, Lucas C, Mackie S, Carachi R. Audit of<br />
ventriculoperitoneal shunt infections in paediatric<br />
patients, 2006–2013. Scott Med J. 2014;59(4):198-203.<br />
doi:10.1177/0036933014548665.<br />
20. Muralidharan R. External ventricular drains: Management and<br />
complications. Surg Neurol Int. 2015;6(Suppl 6):S271-S274.<br />
doi:10.4103/2152-7806.157620.<br />
21. O&#039;Neill BR, Velez DA, Braxton EE, Whiting D, Oh MY. A survey<br />
of ventriculostomy and intracranial pressure monitor placement<br />
practices. World Neurosurg. 2008;70(3):268-273. doi:10.1016/j.<br />
surneu.2007.05.007.<br />
22. Paramore CG, Turner DA. Relative risks of ventriculostomy<br />
infection and morbidity. Acta Neurochir. 1994;127(1-2):79-84.<br />
23. Park J, Choi Y-J, Ohk B, Chang H-H. Cerebrospinal Fluid Leak<br />
at Percutaneous Exit of Ventricular Catheter as a Crucial Risk<br />
Factor for External Ventricular Drainage-Related Infection in<br />
Adult Neurosurgical Patients. World Neurosurg. 2017;109:1-6.<br />
doi:10.1016/j.wneu.2017.09.190.<br />
24. Sandalcioglu IE, Stolke D. Failure of regular external ventricular<br />
drain exchange to reduce CSF infection. J Neurol Neurosurg<br />
Psychiatr. 2003;74(11):1598–9–authorreply1599. doi:10.1136/<br />
jnnp.74.11.1598-a.<br />
25. Simon TD, Riva-Cambrin J, Srivastava R, et al. Hospital care<br />
for children with hydrocephalus in the United States: utilization,<br />
charges, comorbidities, and deaths. J Neurosurg Pediatr.<br />
2008;1(2):131-137. doi:10.3171/PED/2008/1/2/131.<br />
26. Simpkins CJ. Ventriculoperitoneal shunt infections in patients with<br />
hydrocephalus. Pediatr Nurs. 2005;31(6):457-462.<br />
27. Smith RW, Alksne JF. Infections complicating the use of external<br />
ventriculostomy. J Neurosurg. 1976;44(5):567-570. doi:10.3171/<br />
jns.1976.44.5.0567.<br />
28. Tunkel AR, Hasbun R, Bhimraj A, et al. 2017 Infectious Diseases<br />
Society of America’s Clinical Practice Guidelines for Healthcare-<br />
Associated Ventriculitis and Meningitis. Clin Infect Dis.<br />
2017;64(6):e34-e65. doi:10.1093/cid/ciw861.<br />
29. Tunthanathip T, Kanjanapradit K, Sae-Heng S, Oearsakul T,<br />
Sakarunchai I. Predictive factors of the outcome and intraventricular<br />
rupture of brain abscess. J Med Assoc Thai. 2015;98(2):170-180.<br />
30. Vinchon M, Dhellemmes P. Cerebrospinal fluid shunt infection: risk<br />
factors and long-term follow-up. Childs Nerv Syst. 2006;22(7):692-<br />
697. doi:10.1007/s00381-005-0037-8.<br />
31. Wong GKC, Poon WS, Wai S, Yu LM, Lyon D, Lam JMK. Failure<br />
of regular external ventricular drain exchange to reduce cerebrospinal<br />
fluid infection: result of a randomised controlled trial. J Neurol<br />
Neurosurg Psychiatr. 2002;73(6):759-761.]]></dcterms:references>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1280">
    <dcterms:title><![CDATA[Neurocitoma central: a propósito de un caso]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Reporte de Caso]]></dcterms:description>
    <dcterms:abstract><![CDATA[Introducción: El neurocitoma central fue descripto por primera vez en 1982 por Hassoun et al. Se trata de una neoplasia rara,<br />
bien diferenciada del sistema nervioso central de origen neuroectodermico, ubicado más comúnmente a nivel del sistema<br />
ventricular, típicamente adyacente al foramen de Monro. Cursa generalmente con síntomas de hipertensión intracraneal<br />
secundaria a hidrocefalia no comunicante. Afecta generalmente a adultos jóvenes, con edad de presentación media de 29<br />
años en las mayores series descriptas.<br />
Objetivos: Describir y presentar un caso de tumor cerebral específico, cuya importancia se da debido a su baja prevalencia y<br />
escasa casuística relatada en la literatura.<br />
Descripción del caso: En el presente artículo describimos un caso de una paciente de 35 años diagnosticada incidentalmente con<br />
una lesión ocupante de espacio a nivel del ventrículo lateral izquierdo redondeada, heterogénea, de bordes netos con dimensiones<br />
de 40x30x30 mm. La paciente fue intervenida quirúrgicamente para su resección. Se realizó abordaje interhemisférico transcalloso<br />
homolateral. Sin intercurrencias post-quirúrgicas fue dada de alta 4 días luego de la cirugía. El informe anatomo-patológico<br />
demostró tratarse de un Neurocitoma Central. Se comparó nuestro caso con lo descripto en la literatura.<br />
Conclusión: El neurocitoma central a pesar de no ser una patología prevalente, debe ser conocido en profundidad por los<br />
neurocirujanos, ya que su correcto manejo afecta directamente al pronóstico de los pacientes.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Introduction: The central neurocytoma was first described in 1982 by Hassoun et al. It is a rare, well-differentiated neoplasm<br />
of the central nervous system of neuroectodermal origin, located most commonly at the level of the ventricular system,<br />
typically adjacent to the foramen of Monro. It usually presents with symptoms of intracranial hypertension secondary to noncommunicating<br />
hydrocephalus. It generally affects young adults, with an average age of presentation of 29 years in the largest<br />
series described.<br />
Objetives: Describe and present one case of specific brain tumor, which is important due to its your low prevalence and scarce<br />
casuistic in the literature.<br />
Case presentation: In the present article, we describe a case of a female 35-year-old patient diagnosed incidentally with<br />
a heterogeneus rounded space-occupying lesion at the level of the left lateral ventricle, with net edges and dimensions of<br />
40x30x30mm. The patient was surgically intervened for tumoral resection. We opteded to use a homolateral transcallosal<br />
interhemisferic approach. Without post-surgical complications, she was discharged 4 days after surgery. The anatomopathological<br />
report proved to be a Central Neurocytoma. We compared our case with the existing publications.<br />
Conclusion: Despite being an uncommon tumor, Central Neurocytoma must be well understood by every neurosurgeon,<br />
considering that its adequated management influences the patient´s prognosis directly.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Wellerson Sabat Rodrigues]]></dcterms:creator>
    <dcterms:creator><![CDATA[Matias Baldoncini]]></dcterms:creator>
    <dcterms:creator><![CDATA[Maria V. Montero]]></dcterms:creator>
    <dcterms:creator><![CDATA[Maximiliano Zarco]]></dcterms:creator>
    <dcterms:creator><![CDATA[Luciana Perren]]></dcterms:creator>
    <dcterms:creator><![CDATA[ Agustin Conde]]></dcterms:creator>
    <dcterms:creator><![CDATA[ Santiago Giusta]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Diciembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Julio 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Mayo 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:references><![CDATA[1. Baldoncini Matias et al. Anatomia microquirúrgica y abordajes al central<br />
core cerebral. REV ARGENT NEUROC 2019 VOL. 33, N° 1: 1-13.<br />
2. Figarella-Branger D, Söylemezoglu F, Kleihues P, Hassoun J. Cantral<br />
neurocytoma. In Kleihues P, Cavenee WK. (ed). Pathology and genetics of<br />
tumours of the nervous system. Lyon: IARCPress, 2000:107-109.<br />
3. Hanel, Ricardo Alexandre et al. Neurocitoma central com apresentação<br />
incomum por hemorragia intraventricular: relato de caso. Arq. Neuro-<br />
Psiquiatr. [online]. 2001, vol.59, n.3ª.<br />
4. Hassoun J, Gambarelli D, Grisoli F, Pellet W, Salamon G, Pelliser JF, Toga<br />
M. Central neurocytoma. An electron-microscopic study of two cases. Acta<br />
Neuropathol 1982;56:151-156.<br />
5. Hassoun J, Söylemezoglu F, Gambarelli D, Figarella Branger D, von<br />
Ammon K, Kleihues P. Central neurocytoma: a synopsis of clinical and<br />
histological features. Brain Patholology 1993;3:297-306.<br />
6. Katati MJ, Vílchez R, Ros B, Horcajadas A, Arráez MA, Arjona V. Central<br />
neurocytoma: analysis of three cases and review of the literature. Rev Neurol<br />
1999;28:713-717.<br />
7. Koeller KK, Sandberg GD. From the archives of the AFIP. Cerebral<br />
intraventricular neoplasms: radiologic-pathologic correlation.<br />
Radiographics. 22 (6): 1473-505.<br />
8. Louis DN, Ohgaki H, Wiestler OD, Cavenee WK &quot;WHO Classification<br />
of Tumours of the Central Nervous System. 4th Edition Revised&quot; ISBN:<br />
9789283244929.<br />
9. Mackenzie IR. Central Neurocytoma: histologic atypia, proliferation<br />
potential, and clinical outcome. Cancer. 1999 Apr 1;85(7):1606-10.<br />
10. Nishio S, Morioka T, Suzuki S, Fukui M. Tumours around the foramen of<br />
Monro: clinical and neuroimaging features and their differential diagnosis. J<br />
Clin Neurosci 2002; 9:137-141.<br />
11. Rades D, Fehlauer F. Treatment options for central neurocytoma.<br />
Neurology 2002;59:1268-1270.<br />
12. Robbins P, SegalA, Narula S, et al. Central neurocytoma: a<br />
clinicopathological, immunohistochemical and ultrastructural study of 7<br />
cases. Pathol Res Pract 1995;191:100-111.<br />
13. Smith A, Smirniotopoulos J, Horkanyne-Szakaly I. From the Radiologic<br />
Pathology Archives: Intraventricular Neoplasms: Radiologic-Pathologic<br />
Correlation. Radiographics. 2013;33 (1): 21-43.<br />
14. Schild SE, Scheithauer BW, Haddock MG, Schiff D, Burger PC, Wong<br />
WW, Lyons MK. Central neurocytomas. Cancer 1997;79:790-795.<br />
15. Zhang B, Luo B, Zhang Z, Sun G, Wen J. Central neurocytoma:<br />
a clinicopathological and neuroradiological study.Neuroradiology<br />
2004;46:888-895.]]></dcterms:references>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1279">
    <dcterms:title><![CDATA[Seguridad del tratamiento quirúrgico en aneurismas<br />
cerebrales no rotos, en la región de Coquimbo, Chile]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Artículo Original]]></dcterms:description>
    <dcterms:abstract><![CDATA[Introducción: El tratamiento microquirúrgico de los aneurismas cerebrales no rotos, ha demostrado ser seguro en distintas<br />
series, la indicación quirúrgica en estos casos es discutible y generalmente esta en relación a su riesgo de sangrado por<br />
características morfológicas y ubicación del aneurisma. Este trabajo tiene como objetivo, determinar si en nuestra región,<br />
el tratamiento microquirúrgico de los aneurismas cerebrales no rotos es seguro y así poder dar una recomendación de<br />
tratamiento a nuestros pacientes.<br />
Materiales y métodos: Treinta y un pacientes, 33 aneurismas cerebrales no rotos fueron tratados, En clínica Elqui y Hospital<br />
San Pablo de la Región de Coquimbo, entre mayo del 2017 y marzo del 2019, se hizo un seguimiento al total de los pacientes<br />
y se evaluó su resultado neurológico según la escala de Rankin modificado.<br />
Resultado: 97% de los pacientes obtuvieron un resultado neurológico favorable (Rankin &lt; 3), solo un 3% de los pacientes, un<br />
caso, obtuvo un resultado desfavorable (Rankin &gt; 2).<br />
Conclusión: El tratamiento microquirúrgico de los aneurismas cerebrales no rotos en nuestra región es seguro, obteniendo una<br />
muy baja morbilidad y 0% de mortalidad.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Introduction: The microsurgical treatment of unruptured cerebral aneurysms has been shown to be safe in different series,<br />
the surgical indication in these cases is debatable and is generally related to the risk of bleeding due to morphological<br />
characteristics and location of the aneurysm. The objective of this work is to determine if in our region the microsurgical<br />
treatment of unruptured cerebral aneurysms is safe and thus be able to give a recommendation of treatment to our patients.<br />
Materials and methods: 31 patients, 33 unruptured cerebral aneurysms were treated. At the Elqui clinic and San Pablo<br />
Hospital in the Coquimbo Region, between may 2017 and March 2019, the total number of patients was monitored and their<br />
Neurological outcome according to the modified Rankin scale.<br />
Result: 97% of the patients obtained a favorable neurological outcome (Rankin &lt;3), only 3% of the patients, one case, obtained<br />
an unfavorable outcome (Rankin&gt; 2).<br />
Conclusion: The microsurgical treatment of unruptured cerebral aneurysms in our region is safe, obtaining a very low morbidity<br />
and 0% mortality.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[José Tomas Hortal]]></dcterms:creator>
    <dcterms:creator><![CDATA[Jesús Garcia]]></dcterms:creator>
    <dcterms:creator><![CDATA[Iván Perales]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Diciembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Agosto 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Mayo 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:references><![CDATA[1. Ajiboye, Norman, Nohra, Starke, Unruptured Cerebral Aneurysms:<br />
Evaluation and Management. Scientific World Journal. 2015.<br />
954954.<br />
2. Britz GW, Salem L, Newell DW, Eskridge J, Flum DR. Impact of<br />
surgical clipping on survival in unruptured and ruptured cerebral<br />
aneurysms: a population-based study. Stroke. 2004. 35: 1399-1403.<br />
3. Brown R. D, Broderick J. P. Unruptured intracranial aneurysms:<br />
Epidemiology, natural history, management options, and familial<br />
screening. Lancet Neurology. 2014. 1: 393-404.<br />
4. Kotowski M, Naggara O, Darsaut TE, Nolet S, Gevry G,<br />
Kouznetsov E. Safety and occlusion rates of surgical treatment of<br />
unruptured intracranial aneurysms: a systematic review and meta<br />
- analysis of the literature from 1990 to 2011. Journal Neurology<br />
Neurosurgery Psychiatry. 2013. 84: 42-48.<br />
5. Morgan MK, Wiedmann M, Assaad NN, Heller GZ. Complicationeffectiveness<br />
analysis for unruptured intracranial aneurysm surgery:<br />
a prospective cohort study. Neurosurgery. 2016. 78: 648-659.<br />
6. Naggara ON, White PM, Guilbert F, Roy D, Weill A, Raymond<br />
J. Endovascular treatment of intracranial unruptured aneurysms:<br />
systematic review and meta-analysis of the literature on safety and<br />
efficacy. Radiology. 2010. 256: 887-897.<br />
7. Pandey A. S, Gemmete J. J, Wilson T. J, Chaudhary N, Thompson B.<br />
G, Morgenstern L. B, Burke J. F. High Subarachnoid Hemorrhage<br />
Patient Volume Associated with Lower Mortality and Better<br />
Outcomes. Neurosurgery. 2015. 77(3): 462–470.<br />
8. Raaymakers TW, Rinkel GJ, Limburg M, Algra A. Mortality and<br />
morbidity of surgery for unruptured intracranial aneurysms: a metaanalysis.<br />
Stroke. 1998. 29: 1531-1538.<br />
9. Ruan C, Long H, Sun H, He M, Yang K, Zhang H. Endovascular<br />
coiling vs. surgical clipping for unruptured intracranial aneurysm: a<br />
meta-analysis. British Journal Neurosurgery. 2015. 29: 485-492.<br />
10. Spetzler R, McDougall C, Zabramski JM, Albuquerque F, Hills<br />
N, Russin J. The Barrow Ruptured Aneurysm Trial: 6-year results.<br />
Journal Neurosurgery. 2015. 123: 609-617.<br />
11. Thines L, Bourgeois P, Lejeune JP. Surgery for unruptured<br />
intracranial aneurysms in the ISAT and ISUIA era. Canadian<br />
Journal Neurological Sciences. 2012. 39:174-179.<br />
12. Whisnant J, Forbes G. International Study of Unruptured<br />
Intracranial Aneurysms Investigators. Unruptured intracranial<br />
aneurysms risk of rupture and risks of surgical intervention. New<br />
England Journal of Medicine. 1998. 339:1725-1733.<br />
13. Wiebers D. O, Whisnant J. P, Huston J. Unruptured intracranial<br />
aneurysms: natural history, clinical outcome, and risks of surgical<br />
and endovascular treatment. The Lancet. 2003. 362: 103-110.<br />
14. Williams L. N, Brown R. D, Management of unruptured intracranial<br />
aneurysms. Neurology: Clinical Practice. 2013. 3: 99–108.<br />
15. Zheng J, Xu R, Guo Z, Sun X. Small ruptured intracranial<br />
aneurysms: the risk of massive bleeding and rebleeding. Neurological<br />
Research. 2019. 41: 1-7.]]></dcterms:references>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1278">
    <dcterms:title><![CDATA[Cirugía mínimamente invasiva en el tratamiento de<br />
fracturas tóracolumbares]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Artículo Original]]></dcterms:description>
    <dcterms:abstract><![CDATA[Objetivo: Analizar y describir una serie de fracturas tóraco-lumbares traumáticas tratadas con cirugía mínimamente invasiva.<br />
Material y métodos: Analizamos una serie de 26 pacientes con fracturas traumáticas tóraco-lumbosacras entre 2010-2017.<br />
Las imágenes pre-operatorias fueron clasificadas usando la clasificación AO. Analizamos en forma pre y post operatoria:<br />
escala visual analógica, volumen de pérdida sanguínea, duración de la hospitalización, complicaciones, cirugías asociadas en<br />
otros órganos, extracción de implantes en el largo plazo, estado neurológico pre y post quirúrgico y mortalidad.<br />
Los pacientes con historias clínicas completas, TAC pre-operatoria y un seguimiento mínimo de 12 meses fueron incluidos (18<br />
hombres y 8 mujeres). La edad promedio fue de 28.7 años (21-84 años); seguimiento promedio de 28 meses (13-86 meses).<br />
Dieciocho pacientes fueron manejados con instrumentaciones percutáneas, 8 recibieron vertebroplastias, y en 5 casos se<br />
realizó además algún gesto de artrodesis.<br />
Resultados: La EVA mejoró 7 puntos promedio respecto al pre-operatorio; el promedio de sangrado fue de 40 mL, no<br />
observamos ningún caso de empeoramiento neurológico. La duración promedio de la hospitalización fue de 3.9 días. Cuatro<br />
enfermos necesitaron alguna cirugía en otro órgano producto de sus politraumatismos.<br />
Los tornillos percutáneos fueron removidos en 9 casos luego de la consolidación. Como complicaciones tuvimos: 1 hematoma<br />
retroperitoneal autolimitado, una fractura pedicular y una cánula de cementación rota adentro de un pedículo.<br />
Conclusión: La cirugía mínimamente invasiva en trauma espinal es una alternativa válida que permite estabilización,<br />
movilización precoz y logra buenos resultados en términos de control del dolor con baja tasa de complicaciones]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Objective: To analyze and describe a series of trauma-related thoraco-lumbo-sacral vertebral fractures managed with minimally<br />
invasive surgery.<br />
Methods: We retrospectively review the charts and images of 26 patients with thoracolumbar spine fractures between 2010-2017.<br />
Pre-op images were assessed and fractures were classified according to the thoraco-lumbar trauma AO Spine classification. We<br />
analyzed pre and post-surgical visual analog scale (VAS), blood loss during surgery, hospital length of stay, complications, associated<br />
surgical procedures, long term post-op implant removal, pre and post neurological status and mortality.<br />
Patients with a complete case record, pre-op CT scans and minimum 12-month follow up were included (18 males and 8 females).<br />
Mean age was 28.7 years (21-84 years); mean post-op follow up was 28 month (13-86 months). Eighteen patients were managed<br />
with percutaneous instrumentation, 8 patients also received percutaneous vertebroplasty, and 5 patients underwent also some<br />
arthrodesis procedure.<br />
Results: VAS improved 7 points as compared to the pre-op score; mean blood loss was 40 mL, we did not observed any<br />
neurological deficit worsening. Mean hospital length of stay was 3.9 days. Four patients needed surgical procedures involving other<br />
organs due to politrauma.<br />
Percutaneous screws were removed in 9 cases after fracture consolidation. Complications were: one case of self-limiting<br />
retroperitoneal hematoma, one case of pedicle screw fracture and one cement broken cannula into the pedicle.<br />
Conclusion: Minimally invasive surgery in spine trauma is a valid option allowing stabilization, early mobilization, and leading to good<br />
outcomes in terms of pain control and a lower complication rate.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Alfredo Guiroy]]></dcterms:creator>
    <dcterms:creator><![CDATA[ Federico Landriel]]></dcterms:creator>
    <dcterms:creator><![CDATA[Alejandro Morales Ciancio]]></dcterms:creator>
    <dcterms:creator><![CDATA[Santiago Hem]]></dcterms:creator>
    <dcterms:creator><![CDATA[Alfredo Sícoli<br />
]]></dcterms:creator>
    <dcterms:creator><![CDATA[Nicolás Gonzalez Masanés]]></dcterms:creator>
    <dcterms:creator><![CDATA[ Martín Gagliardi]]></dcterms:creator>
    <dcterms:creator><![CDATA[Claudio Yampolsky]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Diciembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Junio 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Junio 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:references><![CDATA[1. Alander D, Cui S. Percutaneous pedicle screw stabilization: surgical<br />
technique, fracture reduction, and review of current spine trauma<br />
applications. J Am Acad Orthop Surg 2018; 0:1-10.<br />
2. Bakhsheshian J, Dahdaleh N, Fakurnejad S, Scheer J, Smith Z. Evidencebased<br />
management of traumatic thoracolumbar burst fractures: a systematic<br />
review of nonoperative management. Neurosurg Focus 2014; 37 (1):E1.<br />
3. Bose D, Tejwani NC. Evolving trends in the care of polytrauma patients.<br />
Injury, Int. J. Care Injured 2006; 37, 20-28.<br />
4. Denis F. The three column spine and its significance in the classification of<br />
acute thoracolumbar spinal injuries. Spine (Phila Pa 1976) 1983;8:817–831.<br />
5. Hitchon P, Abode-Iyamah K, Dahdaleh N, Shaffrey C, Noeller J, He<br />
W, Moritani T. Nonoperative management in neurologically intact<br />
thoracolumbar burst fractures: clinical and radiographic outcomes. Spine<br />
2016;41:483–489.<br />
6. Laghmouche N, Prost S, Farah K, Graillon T, Blondel B, Fuentes S.<br />
Minimally invasive treatment of thoracolumbar flexion-distraction fracture.<br />
Orthop Traumatol Surg Res. 2019 Apr;105(2):347-350.<br />
7. Landi A, Marotta N, Mancarella C, Meluzio M, Pietrantonio A, Delfini R.<br />
Percutaneous short fixation vs conservative treatment: comparative analysis<br />
of clinical and radiological outcome for A.3 burst fractures of thoracolumbar<br />
junction and lumbar spine. Eur Spine J 2014; 23 (Suppl 6):S671–<br />
S676.<br />
8. Pape HC, Giannoudis P, Krettek C. The timing of fracture treatment in<br />
polytrauma patients: relevance of damage control orthopedic surgery. The<br />
American Journal of Surgery 183. 2002; 622–629.<br />
9. Pape H et al. The poly-traumatized patient with fractures: a multidisciplinary<br />
approach. 2016. Springer-Verlag Berlin Heidelberg. DOI<br />
10.1007/978-3-662-47212-5_14.<br />
10. Resnik DK, Weller SJ, Benzel EC. Biomechanics of the thoracolumbar<br />
spine. Neurosurg Clin North Am 8:455-469, 1997.<br />
11. Rodríguez Boto G, Vaquero Crespo J. Traumatismo raquimedular. Pág 1-2.<br />
ISBN 978-84-7978-905-3.<br />
12. Scalea TM, Boswell SA, Scott JD, et al. External fixation as a bridge to<br />
intramedullary nailing for patients with multiple injuries and with femur<br />
fractures: damage control orthopaedics. J Trauma 2000;48: 613–23.<br />
13. Stahel P, VanderHeiden T, Flierl M, Matava B, Gerhardt D, Bolles G,<br />
Beauchamp K, Burlew C, Johnson J, Moore E. The impact of a standardized<br />
‘‘spine damage-control’’ protocol for unstable thoracic and lumbar spine<br />
fractures in severely injured patients: A prospective cohort study. J Trauma<br />
Acute Care Surg 590 Volume 74, Number 2.<br />
14. Tian F, Tu LY, Gu WF, Zhang EF, Wang ZB, Chu G, Ka H, Zhao J.<br />
Percutaneous versus open pedicle screw instrumentation in treatment of<br />
thoracic and lumbar spine fractures, a systematic review and metaanalysis.<br />
Medicine (Baltimore). 2018 Oct; 97(41):e12535.<br />
15. Vaccaro A, Oner C, Kepler C, Dvorak M, Schnake K et al. AOSpine<br />
Thoracolumbar Spine Injury Classification System. Spine 2013;38:2028–<br />
2037.<br />
16. Wang X, Liu Y, Wang X, Chen H, Cao P, Tian Y, Wu X, Chen Y, Yuan<br />
W. Beneficial effects of percutaneous minimally invasive surgery for patients<br />
with fractures in the thoracic spine. Exp Ther Med. 2018 Dec;16(6):5394-<br />
5399.<br />
17. Yaszemski MJ, White AA, Panjabi MM. Biomechanics of the spine. En:<br />
Fardon DF, Garfin SR, Abitbol J-J, Boden SD, Herkowitz HN, Mayer TG<br />
(Eds.), Orthopaedic Knowledge Update: Spine 2, American Academy of<br />
Orthopaedic Surgeons, Illinois, 2002, pp. 15-23, Cap. 3.]]></dcterms:references>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1277">
    <dcterms:title><![CDATA[Tumor de plexo braquial con extensión cervico torácica<br />
en paciente pediátrico]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Reporte de Caso]]></dcterms:description>
    <dcterms:abstract><![CDATA[Introducción: Los tumores de plexo braquial constituyen una entidad infrecuente. Cuando la lesión cumple con criterios<br />
quirúrgicos, el tratamiento ideal es la exéresis completa.<br />
Descripción del caso: Paciente pediátrica con antecedentes de neurofibromatosis que consulta por dolor leve y parestesias<br />
episódicas. Presenta masa palpable en región supraclavicular izquierda de consistencia duro elástica con signo de Tinel<br />
negativo. Se realiza una exéresis completa del neurofibroma mediante una cervicotomía anterior.<br />
Discusión: La indicación quirúrgica fue realizada en base al crecimiento tumoral y su efecto de masa sobre estructuras<br />
contiguas, los trastornos sensitivos y su antecedente de NF1, que predispone a variantes malignas. La clavícula suele ser el<br />
elemento anatómico que define las principales vías de abordaje al plexo braquial.<br />
Conclusión: Dejamos reportado un caso de neurofibroma de plexo braquial en una paciente pediátrica con neurofibromatosis.<br />
Describimos como la cervicotomía anterior fue una excelente vía a una masa extensión cervico torácica.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Introduction: Brachial plexus tumors are an infrequent entity. When the lesion meets surgical criteria, the ideal treatment is its<br />
complete removal.<br />
Case report: A pediatric patient with a history of neurofibromatosis consults for mild pain and episodic paresthesias. The patient<br />
presented to the hospital for an elastic palpable mass in the left supraclavicular region testing negative for Tinel&#039;s sign. Complete<br />
removal of the neurofibroma was performed through an anterior cervicotomy.<br />
Discussion: The surgical indication was made based on the growth of the tumor and its mass effect on contiguous structures, the<br />
patient’s sensory disorders and her neurofibromatosis history, which predisposes to malignant variants. The clavicle is usually the<br />
anatomical element defining the main approaches to the brachial plexus.<br />
Conclusion: The purpose of this article was to present a case of a of brachial plexus neurofibroma in a pediatric patient with<br />
neurofibromatosis. The anterior cervicotomy it would seem to be an excellent approach to a cervical thoracic extension mass.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Jorge Luis Bustamante]]></dcterms:creator>
    <dcterms:creator><![CDATA[Nicolas Tello]]></dcterms:creator>
    <dcterms:creator><![CDATA[Lucas Hinojosa]]></dcterms:creator>
    <dcterms:creator><![CDATA[Ariel Perelló]]></dcterms:creator>
    <dcterms:creator><![CDATA[Marcelo D’Agustini]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Diciembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Agosto 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Marzo 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:references><![CDATA[1. Bandiera A, Negri G, Melloni G, Mandelli C, Gerevini S, Carretta A, et<br />
al. Management of Intrathoracic Benign Schwannomas of the Brachial<br />
Plexus. Case Rep Surg. 2014;2014:1-3.<br />
2. Courvoisier LG. Die Neurome eine Klinische Monographie. Basel,<br />
Switzerland: B Schwode; 1886.<br />
3. Das S, Ganju A, Tiel RI, Kline DG. Tumors of the brachial plexus.<br />
Neurosurg Focus 2007;22(6):1-6.<br />
4. Hirbe AC, Gutmann DH. Neurofibromatosis type 1: a multidisciplinary<br />
approach to care. Lancet Neurol 2014; 13: 834–43.<br />
5. Jia X, Yang J, Chen L, Yu C, Kondo T. Primary Brachial Plexus Tumors:<br />
Clinical Experiences of 143 Cases. Clin Neurol Neurosurg. 2016;148:91-5.<br />
6. Lee HJ, Kim JH, Rhee SH, Gong HS, Baek GH. Is surgery for brachial<br />
plexus schwannomas safe and effective?. Clin Orthop Relat Res.<br />
2014;472:1893-8.<br />
7. Lwu S, Midha R. Clinical examination of brachial and pelvic plexus tumors.<br />
Neurosurg Focus. 2007;22(6):1-5.<br />
8. Millan G, Casal D. Brachial plexus tumors in a tertiary referral center: a case<br />
series and literature review. Acta Reumatol Port. 2015;40:372-7.<br />
9. Oré Acevedo JF, La Torre Caballero M, Urteaga Quiroga R. Neurofibroma<br />
cervical pediátrico. Reporte de caso. An Fac med. 2016;77(3):287-9.<br />
10. Tschoe C, Holsapple JW, Binello E. Resection of primary brachial<br />
plexus tumor via a modified supraclavicular approach. J Neurol Surg Rep<br />
2014;75:133-5.]]></dcterms:references>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1276">
    <dcterms:title><![CDATA[Volumen 33 Número 3]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1275">
    <dcterms:title><![CDATA[MI AMIGO, EL COMANDANTE RENZI]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Editorial]]></dcterms:description>
    <dcterms:creator><![CDATA[Remberto Burgos de la Espriella]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1274">
    <dcterms:title><![CDATA[EDITORIAL]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Editorial]]></dcterms:description>
    <dcterms:creator><![CDATA[Álvaro Campero]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Septiembre 2019]]></dcterms:date>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1273">
    <dcterms:title><![CDATA[Otomastoiditis crónica supurada complicada con absceso<br />
extradural y colecciónsupurada subcutánea (Absceso de<br />
Bezold), asociada a hematoma subdural crónico]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Reporte de Caso]]></dcterms:description>
    <dcterms:abstract><![CDATA[Introducción: Las complicaciones intracraneanas de la otomastoiditis crónica supurada (OMCS) se ven cada vez con menor<br />
frecuencia gracias al diagnóstico precoz, acceso a imagenología y uso de antibióticos. La asociación de una OMCS con<br />
empiema extradural y hematoma subdural crónico es extremadamente infrecuente y y reportar un caso clinico es el objetivo de<br />
este reporte.<br />
Caso clínico: Paciente de 28 años, con historia de trauma craneano dos meses antes del ingreso. Consultó por otorrea fétida<br />
derecha de 45 días de evolución. Un mes previo a la consulta instala tumoración fluctuante en planos superficiales de región<br />
temporoparietal derecha que aumenta de tamaño y se hace dolorosa. Examen neurológico normal.<br />
Se realiza tomografía de cráneo que evidencia colección extradural y subdural, asociada a otomastoiditis. Se intervino<br />
en conjunto con ORL para evacuación del proceso supurado intracraneano y mastoidectomía, encontrándose en el<br />
intraoperatorio que la colección subdural no era infecciosa (empiema), sino que era un hematoma subdural crónico. La<br />
evolución fue buena siendo dado de alta asintomático.<br />
Reportamos esta asociación lesional muy poco frecuente, cuyo diagnóstico preoperatorio hubiera hecho variar la táctica<br />
neuroquirúrgica. Se discuten los hechos clínicos e imagenológicos que podrían haber llevado al diagnóstico correcto.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Introduction: Intracranial complications of chronic suppurative otomastoiditis (OMCS) are seen less and less frequently seen<br />
thanks to early diagnosis, access to imaging and access to antibiotics. The association of an OMCS with extradural empyema<br />
and chronic subdural hematoma is extremely infrequent. We report a clincal case of OMCS associated with a chronic subdural<br />
haematoma.<br />
Clinical case: A 28-year-old patient with a history of cranial trauma two months before admission, who consulted for a 46-<br />
day history of fetid otorrhea. One month prior to the consultation, he detected a fluctuating tumor in superficial planes of the<br />
right temporoparietal region that increased and became painful. He has a normal neurological examination. We performed a<br />
cranial CT and we detected an extradural and subdural collection, associated with otomastoiditis. A surgical intervention with<br />
a combined team was performed (Othologist and neurosurgeons). The aim of the surgery to evacuate the intracranial process<br />
and mastoidectomy. In the intraoperative period, we discovered that the subdural collection was not infectious but a chronic<br />
subdural hematoma. The evolution was good being discharged asymptomatic.<br />
We report a very rare association (OMCS with chronic subdural haematoma), whose preoperative diagnosis would have<br />
changed the neurosurgical tactic. Clinical and imaging facts that could have led to the correct diagnosis are discussed.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Gabriel Charlone Granucci]]></dcterms:creator>
    <dcterms:creator><![CDATA[Gonzalo Bertullo]]></dcterms:creator>
    <dcterms:creator><![CDATA[Fernando Martínez]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Septiembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Agosto 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Abril 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
    <dcterms:bibliographicCitation><![CDATA[1. Artenstein AW, Kim JH, Schmidek HH. Suppurative intracranial<br />
infections. In: Schmidek HH, Sweet H.(Eds). Operative neurosurgical<br />
techniques. Fourth edition. WB Saunders. Philadelphia 2000:1685-1693.<br />
2. Bernaldez PC, Morales G, Quantin LG, Hernández C, Litterio M. Otitis<br />
media crónica supurada en niños. Arch Argent Pediatr 2004;102(3):174-179.<br />
3. Burakgazi G, Bayaroğullari H, Öztürk F, et al. Radiological imaging of<br />
rare intracranial complications secondary to otitis media and mastoiditis. J<br />
Craniofac Surg. 2017;28(3):620-624.<br />
4. Compean Aguilar A, Gutierrez Butando J, Azuano Pliego E, Reyes<br />
Miranda R. Complicaciones de otitis media en el niño. Experiencia del<br />
OTOMASTOIDITIS CRÓNICA SUPURADA COMPLICADA CON ABSCESO EXTRADURAL Y COLECCIÓNSUPURADA SUBCUTÁNEA (ABSCESO DE BEZOLD),<br />
ASOCIADA A HEMATOMA SUBDURAL CRÓNICO<br />
Gabriel Charlone Granucci, Gonzalo Bertullo, Fernando Martínez<br />
REV ARGENT NEUROC. VOL. 33, N° 3: 175-179 | 2019 REPORTE DE CASO<br />
179<br />
Instituto Nacional de Pediatría. Acta Ped Mex 1997;18(1):28-33.<br />
5. Coutinho G, Júlio S, Matos R, Santos M, Spratley J. Otogenic cerebral<br />
venous thrombosis in children: A review of 16 consecutive cases. Int J<br />
Pediatr Otorhinolaryngol 2018;113:177-181.<br />
6. Chen JCT, Levy ML. Causes, epidemiology, and risk factors of chronic<br />
subdural hematoma. Neurosurg Clin NA 2000;11(3):399-406.<br />
7. Fogelholm R, Heiskanen O, Waltimo O. Chronic subdural hematoma<br />
in adults. Influence of patient´s age on symptoms, signs and thickness of<br />
hematoma. J Neurosurg 1975;42:43-46.<br />
8. Hafidh MA, Keogh I, Mc Nonn Walsh R, Walsh M, Rawluk D. Otogenic<br />
intracranial complications. A 7-years retrospective review. Am J Otolaringol<br />
2006;27:390-395.<br />
9. Jain A, Arora N, Meher R, Passey JC, Bansal R. Intracranial complications<br />
of CSOM in pediatric patients: A persisting problem in developing<br />
countries. Int J Pediatr Otorhinolaryngol. 2017;100:128-131.<br />
10. Martínez F. Presentación clínica del hematoma subdural crónico en adultos:<br />
el gran simulador. Rev Med Uruguay 2007;23:92-98.<br />
11. Martínez F, Mañana G, Panuncio A, Laza S. Revisión anatomo-clínica de<br />
las meninges y espacios intracraneanos con especial referencia al hematoma<br />
subdural crónico. Rev Mex Neurocien 2008;9(1):47-60.<br />
12. Schneider S, Kapelushnik J, Kraus M, El Saied S, Levi I, Kaplan DM. The<br />
association between otogenic lateral sinus thrombosis and thrombophilia -<br />
A long-term follow-up. Am J Otolaryngol. 2018;39(3):299-302.<br />
13. Van der Poel NA, van Spronsen E, Dietz de Loos DA, Ebbens FA. Early<br />
signs and symptoms of intracranial complications of otitis media in pediatric<br />
and adult patients: A different presentation? Int J Pediatr Otorhinolaryngol.<br />
2017;102:56-60.]]></dcterms:bibliographicCitation>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1272">
    <dcterms:title><![CDATA[Resección microquirúrgica de meningioma<br />
de la región pineal]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Video]]></dcterms:description>
    <dcterms:abstract><![CDATA[Introducción: Los meningiomas de la región pineal son lesiones poco frecuentes, representando el 2 al 8% de los tumores<br />
localizados en esta área. Estos tumores son lesiones con comportamiento biológicamente benigno y potencialmente curables<br />
con la resección quirúrgica radical. A su vez representan un desafío quirúrgico debido a su profunda localización y la cercanía<br />
de estructuras anatómicas vitales. El abordaje supracerebeloso infratentorial, en posición semisentado (cuando las condiciones<br />
generales del paciente lo permiten), provee un corredor natural a la región pineal mediante la retracción cerebelosa gravitatoria.<br />
Objetivo: Presentación de la exéresis microquirúrgica completa de un meningioma de la región pineal.<br />
Descripción del caso: Paciente de 52 años que consulta por inestabilidad de la marcha y diplopía de 2 semanas de evolución.<br />
La resonancia magnética cerebral mostró una lesión expansiva, que realza con contraste, de 43 x 30 mm en la región<br />
pineal, con hidrocefalia obstructiva acompañante. Se realiza la exéresis microquirúrgica mediante abordaje supracerebeloso<br />
infratentorial con el paciente en posición semisentado.<br />
Resultado: Se realizó la exéresis completa de la lesión. La paciente cursó el primer día postoperatorio en Unidad de Terapia<br />
Intensiva y luego pasó a sala de internación general. Fue dada de alta al tercer día, sin déficit neurológico. La anatomía<br />
patológica de la lesión informó meningioma transicional (OMS grado I). El control imagenológico postquirúrgico mostró la<br />
resección de la lesión sin remanente tumoral.<br />
Conclusión: Los meningiomas de la región pineal presentan un desafío quirúrgico debido a la relación con estructuras<br />
anatómicas vitales. El abordaje supracerebeloso infratentorial ofrece un corredor anatómico natural mediante la retracción<br />
cerebelosa por la gravedad.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[Background: Meningiomas of the pineal region are rare lesions representing 2 to 8% of the tumors located in this area. These tumors are<br />
lesions with biologically benign behavior and potentially curable by radical surgical resection. As well, they are a surgical challenge due to<br />
their deep location and the proximity to vital anatomical structures. The supracerebellar infratentorial approach, in a semisitting position<br />
(when the patient’s general conditions allow it), provides a natural corridor to the pineal region through gravitational cerebellar retraction.<br />
Objetive: Presentation of a complete microsurgical resection of a meningioma of the pineal region.<br />
Case description: A 52-year-old patient who consulted due to gait instability and diplopia of 2 weeks of evolution. Brain magnetic<br />
resonance showed an expansive lesion, with contrast enhancement, 43 x 30 mm in the pineal region, with obstructive hydrocephalus.<br />
The microsurgical resection was performed by supracerebellar infratentorial approach with the patient in a semisitting position.<br />
Result: The complete microsurgical resection was achieved. The patient spent the first postoperative day in Intensive Care Unit,<br />
and then went to general room. He was discharged on the third postoperative day, without neurological deficit. The histopathology<br />
assessment of the lesion reported transitional meningioma (WHO grade I). Post-surgical imaging showed the resection of the lesion<br />
without remaining tumor.<br />
Conclusion: Meningiomas of the pineal region present a surgical challenge due to the relationship with vital anatomical structures.<br />
The supracerebellar infratentorial approach offers a natural anatomical corridor through cerebellar retraction by gravity.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Pablo Ajler]]></dcterms:creator>
    <dcterms:creator><![CDATA[Jorge Rasmussen]]></dcterms:creator>
    <dcterms:creator><![CDATA[Pedro Plou]]></dcterms:creator>
    <dcterms:creator><![CDATA[Álvaro Campero]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Septiembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Agosto 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Julio 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:references><![CDATA[1. Inoue A, Ohnishi T, Kohno S, Ohtsuka Y, Nakamura Y, Mizuno Y,<br />
Kitazawa R, Ohue S. Two cases of pineal-region meningiomas derived from<br />
arachnoid membrane over the vein of Galen without dural attachment.<br />
World J Surg Oncol. 2015 Jul 25;13:226.<br />
2. Konovalov AN, Spallone A, Pitzkhelauri DI. Meningioma of the pineal<br />
region: a surgical series of 10 cases. J Neurosurg. 1996 Oct;85(4):586-90.<br />
3. Otani N, Mori K, Wada K, Tomiyama A, Toyooka T, Takeuchi S.<br />
Multistaged, multidirectional strategy for safe removal of large meningiomas<br />
in the pineal region. Neurosurg Focus. 2018 Apr;44(4):E13.<br />
4. Goto T, Ohata K, Morino M, Takami T, Tsuyuguchi N, Nishio A, Hara M.<br />
Falcotentorial meningioma: surgical outcome in 14 patients. J Neurosurg.<br />
2006 Jan;104(1):47-53.]]></dcterms:references>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1271">
    <dcterms:title><![CDATA[Modelo de neuroendoscopia ventricular “INARUS”]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Nota Técnica]]></dcterms:description>
    <dcterms:abstract><![CDATA[Introducción: La simulación es una herramienta de educación indispensable para un entrenamiento progresivo en un ámbito<br />
seguro, no solo para el paciente sino para el educando. La misma fue incorporada en la curricula de nuestras especialidades<br />
quirúrgicas a partir del 2013. Las habilidades neuroquirúrgicas requieren de un experticio que implica un periodo prolongado<br />
de tiempo de práctica. En la actualidad, dicho periodo, se tiende a disminuir con la enseñanza de ensayo y error, repetición de<br />
los procedimientos y automatización de maniobras que la simulación facilita con el agregado de la posibilidad de un feedback<br />
de retroalimentación entre el profesional en formación y el educador en un ambiente seguro.<br />
Objetivo: Describir un modelo de simulador físico sintético de bajo costo como herramienta inicial para mejorar la curva de<br />
aprendizaje de las técnicas de neuroendoscopia intraventricular.<br />
Descripción del simulador: es un modelo físico sintético realizado a través de técnicas de mordería con gel autoportante. El<br />
simulador ofrece la posibilidad de practicar técnicas básicas neuroendoscópicas intraventriculares, ofreciendo la particularidad<br />
de poder repetir las maniobras y gestos quirúrgicas con un coste beneficio muy elevado debido al muy bajo precio de<br />
realización del simulador. A su vez, se trata de un modelo de simulación que se puede fabricar de forma casera en cualquier<br />
centro de simulación.<br />
Discusión: Presentamos un modelo inédito de bajo costo y alta fidelidad para simulación neuroendoscópica. Consta de<br />
un cerebro sintético físico que permite replicar ejercicios de navegación intraventricular con maniobras endoscópicas,<br />
toma de biopsia de lesiones quísticas o sólidas, sección de tabiques, lavado ventricular y desobstrucción de catéteres<br />
intraventriculares. Lo consideramos una herramienta básica y de amplia ayuda para profesionales que decidan iniciar su curva<br />
de aprendizaje en la neuroendoscopia intraventricular. Planeamos su validación en futuros congresos de neurocirugía.]]></dcterms:abstract>
    <dcterms:creator><![CDATA[Juan Manuel Liñares]]></dcterms:creator>
    <dcterms:creator><![CDATA[Romina Argañaraz]]></dcterms:creator>
    <dcterms:creator><![CDATA[Amparo Sáenz]]></dcterms:creator>
    <dcterms:creator><![CDATA[Patricia Martinez]]></dcterms:creator>
    <dcterms:creator><![CDATA[Marcela Bailez]]></dcterms:creator>
    <dcterms:creator><![CDATA[Beatriz Mantese]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Septiembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Introduction: Simulation is an indispensable educational tool for progressive training in a safe environment, for both patients and<br />
learning neurosurgeons. It was incorporated into the curricula of our surgical specialties as of 2013. Neurosurgical skills require an<br />
expertise that involves a prolonged period of practice time. Currently, this period tends to decrease with the teaching of trial and error,<br />
repetition of procedures and automation of maneuvers that the simulation facilitates with the addition of the possibility of feedback<br />
between the professional in training and the educator, all doing in a safe environment.<br />
Objective: To describe a low cost synthetic physical simulator model as an initial tool to improve the learning curve of intraventricular<br />
neuroendoscopy techniques.<br />
Description of the simulator: it is a synthetic physical model realized through self-supporting gel biting techniques. The simulator<br />
offers the possibility of practicing intraventricular neuroendoscopic basic techniques, offering the peculiarity of being able to repeat<br />
maneuvers and surgical gestures with a very high benefit-cost due to a very low price of its creation. At the same time, it is a<br />
simulation model that can be manufactured at home in any simulation center.<br />
Discussion: We present an unprecedented model of low cost and high fidelity for neuroendoscopic simulation. It consists of a<br />
physical synthetic brain that allows the replication of intraventricular navigation exercises with endoscopic maneuvers, a biopsy<br />
of solid or cystic lesions, the section of the ventricular septum, ventricular lavage and unblocking of intraventricular catheters. We<br />
consider this simulator as a basic tool of wide assistance for professionals who decide to start their learning curve in intraventricular<br />
neuroendoscopy. We’re planning its validation in a future neurosurgery congress.]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Julio 2019]]></dcterms:dateSubmitted>
    <dcterms:issued><![CDATA[Agosto 2019]]></dcterms:issued>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:references><![CDATA[1. Breimer Gerben E., Vivek Bodani, Thomas Looi, and James M.<br />
Drake. Design and evaluation of a new synthetic brain simulator for<br />
endoscopic third ventriculostomy. J Neurosurg Pediatr 15:82–88, 2015.<br />
PMID:25360853.<br />
2. Breimer Gerben E., Simulation-based Education for Endoscopic Third<br />
Ventriculostomy: A Comparison Between Virtual and Physical Training<br />
Models. Operative neurosurgery volume13, number 1, february2017.<br />
PMID:28931258.<br />
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Clinical Experience with Ventricular Lesions. Zentralbl Neurochir 2006;<br />
67: 129–136. PMID: 16958010.<br />
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simulator for pediatric neuroendoscopic practice. Childs Nerv Syst (2015)<br />
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6. Coelho G., Warf B., Lyra M., Zanon N. Anatomical pediatric model for<br />
craniosynostosis surgical training. Childs Nerv Syst (2014) 30:2009–2014.<br />
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7. Craven C., Martyn Cooke, Clare Rangeley, Samuel J. M. M. Alberti, and<br />
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Inform 150:811–815. PMID: 19745425.<br />
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microsurgical training. Journal of Oral and Maxillofacial Surgery, 44(10),<br />
833–836. doi:10.1016/0278-2391(86)90167-9. PMID: 3463717.<br />
10. Filho FV, Coelho G, Cavalheiro S, Lyra M, Zymberg ST (2011) Quality<br />
assessment of a new surgical simulator for neuroendoscopic training.<br />
Neurosurg Focus 30:E17. PMID: 21456928.<br />
11. Jaimovich S. Neurosurgical training with simulators: a novel<br />
neuroendoscopy model. Childs Nerv Syst (2015). PMID: 26493056.<br />
12. Satava RM (2007) The future of surgical simulation and surgical robotics.Bull Am Coll Surg 92(3):13–9. PMID: 17419163.<br />
13. Weber, D., Moser, N., &amp; Rösslein, R. (1997). A Synthetic Model for<br />
Microsurgical Training: A Surgical Contribution to Reduce the Number<br />
of Animal Experiments. European Journal of Pediatric Surgery, 7(04), 204–<br />
206. doi:10.1055/s-2008-1071093. PMID: 9297513.<br />
14. Zymberg, S., Vaz-Guimarães Filho, F., &amp; Lyra, M. (2010). Neuroendoscopic<br />
Training: Presentation of a New Real Simulator. Min - Minimally Invasive<br />
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20376746.<br />
15. Curso Básico de Neuroendoscopia – CeSim – Hospital de Pediatría<br />
Garrahan. Diciembre 2018.]]></dcterms:references>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1270">
    <dcterms:title><![CDATA[“Educar” en cirugía de columna II: evolución en la<br />
neurocirugía nacional frente al cambio permanente y su<br />
relación con la certificación]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Artículos Varios]]></dcterms:description>
    <dcterms:creator><![CDATA[Juan José María Mezzadri]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Septiembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Julio 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Junio 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:references><![CDATA[1. Anand N, Kong C, Fessler RG. A staged protocol for circumferential<br />
minimally invasive surgical correction of adult spinal deformity.<br />
Neurosurgery 2017; 81:733-9.<br />
2. Bateman AH, Larouche J, Goldstein CL, Sciubba DM, Choma TJ,<br />
Lawrence B et al. The importance of determining trainee perspectives on<br />
procedural competencies during spine surgery clinical fellowship. Global<br />
Spine J 2019; 9:18-24.<br />
3. Bauman Z. Vida líquida. Buenos Aires: Paidós, 2006.<br />
4. Boszcyk BM, Mooij JJ, Schmitt N, Di Rocco C, Fakouri BB, Lindsay<br />
KW. Spine surgery training and competence of European Neurosurgical<br />
Trainees. Acta Neurochir 2009; 151:619-28.<br />
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nlmcatalog/journals, 2014.<br />
6. Cómo aprende el cerebro: Neuroeducación y factores del aprendizaje.<br />
https://blog.cognifit.com/es/como-aprende-el-cerebro-neuroeducacion/<br />
abril 30, 2017.<br />
7. Conley C. Liderazgo joven. En el ámbito del trabajo, los 30 son los nuevos 50.<br />
https://www.lanacion.com.ar/economia/liderazgo-joven-en-el-ambito-deltrabajo-<br />
los-30-son-los-nuevos-50-nid2250235, La Nación, mayo 22, 2019.<br />
8. Dvorak MF, Collins JB, Murnaghan L, Hurlbert RJ, Fehlings M, Fox<br />
R et al. Confidence in spine training among senior neurosurgical and<br />
orthopaedic residents. Spine 2006; 31:831-7.<br />
9. Fernández CF, Suárez R. Solidarios y escépticos, el denominador común de<br />
la región. https://www.lanacion.com.ar/sociedad/solidarios-y-escepticos-eldenominador-<br />
comun-de-la-region-nid2244545, La Nación, mayo 5, 2019.<br />
10. Guiroy A, Morales Ciancio A, Fernández Molina F, Jalón P, Gagliardi M,<br />
Mezzadri JJ. Microendoscopic decompression (MED) of the lumbar spine.<br />
Initial experience including 30 cases. MOJ Orthop Rheumatol 6(3):00220,<br />
2016.<br />
11. Herkowitz HN, Weinstein JN, Callaghan JJ, Derosa GP. Spine fellowship<br />
education and its association with the part-II oral certification examination.<br />
J Bone Joint Surg 2006; 88:668-70.<br />
12. Iaies G, Ruibal J. El desafío de entender a la “generación Y”. http://www.<br />
lanacion.com.ar/1661962-el-desafio-de-entender-a-la-generacion-y, La<br />
Nación, febrero 7, 2014.<br />
13. Infante VS. O Perfil da Universidade para o próximo milenio. Educ Policy<br />
Anal Arch 1999; 7:1-13.<br />
14. Karpinski J, Ajjawi R, Moreua K. Fellowship tarining: a qualitative study<br />
of scope and purpose across one department of medicine. BMC Medical<br />
Education 2017; 17:223.<br />
15. Konczalik W, Elsayed S, Boszcyk B. Experience of a fellowship in spinal<br />
surgery: a quantitative analysis. Eur Spine J 2014; 23(Suppl I):S40-S54.<br />
16. Landriel F, Hem S, Rasmussen J, Vecchi E, Yampolsky C. Fusión<br />
intersomática lumbar extraforaminal mínimamente invasiva (MIS-ELIF).<br />
Rev Argent Neuroc 2017; 31:82-9.<br />
17. Larouche J, Yee AJM, Wadey V, Ahn H, Hedden DM, Hall H et al.<br />
Development of a competence-based spine surgery fellowship curriculum<br />
set of learning objectives in Canada. Spine 2016; 41:530-7.<br />
18. Makhni MC, Caldwell JM, Saifi C, Fischer CR, Lehman RA, Lenke<br />
LG et al. Tissue engineering advances in spine surgery. Regen Med. 2016;<br />
11:211-22. Epub 2016 Feb 15. Review.<br />
19. Mariscal E. El espíritu del león. Cuentos sobre el liderazgo en la selva de losnegocios. Buenos Aires: Aguilar, 2004.<br />
20. Mascó A. Entre generaciones. Buenos Aires: Temas Grupo Editorial SRL,<br />
2012.<br />
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Argent Neuroc 2006; 20:147-9.<br />
22. Mezzadri JJ, Gardella JL. Cirugía de columna: ¿con una nueva identidad?<br />
Rev Argent Neuroc 2003; 17:39-42.<br />
23. Mezzadri JJ. “Educar” en cirugía de columna. Rev Argent Neuroc 2007;<br />
21:79-84.<br />
24. Mezzadri JJ. El liderazgo hoy: nuevos desafíos y competencias. Rev Argent<br />
Neuroc 2014; 28:162-5.<br />
25. Mezzadri JJ. Proyecto para un título de especialista: “neurocirujano<br />
especializado en cirugía de columna”. Rev Argent Neuroc 2010; 24:217-22.<br />
26. Ohaegbulam C, Trost GR, Lieberman IH, Eichler ME. Education<br />
and knowledge-base acquisition and retention. En EC Benzel, editor.<br />
Spine surgery: techniques, complication avoidance, and management.<br />
Philadelphia: Elsevier, Inc., 2005, Chapter 20, pp. 252-5.<br />
27. Prieto Gil A. La pirámide del aprendizaje. www.ucm.es/BUCM/revcul/elearning-<br />
innova/27/art1263.pdf.<br />
28. Smith JS, Shaffrey CI, Bess S, Shamji MF, Brodke D, Lenke LG et al.<br />
Recent and emerging advances in spinal deformity. Neurosurgery 2017;<br />
80:S70-S85.<br />
29. Terrile S. Sello generacional. Generar pequeños cambios, la meta de los<br />
jóvenes del país. https://www.lanacion.com.ar/sociedad/sello-generacionalgenerar-<br />
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30. Van Isseldyk F, Nicola T, Pastore J, Frucella G, Rojas H. Discectomía<br />
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Nanotechnology in spine surgery: a current update and critical review of the<br />
literature. World Neurosurg 2019; 123:142-55.]]></dcterms:references>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description><rdf:Description rdf:about="https://aanc.org.ar/ranc/items/show/1269">
    <dcterms:title><![CDATA[Definiendo los alcances de la neuroética]]></dcterms:title>
    <dcterms:subject><![CDATA[Neurocirugía]]></dcterms:subject>
    <dcterms:description><![CDATA[Artículos Varios]]></dcterms:description>
    <dcterms:abstract><![CDATA[El término neuroética define al campo de bioética que se ocupa de los dilemas originados en el desarrollo de las<br />
neurociencias. ¿Por qué nos resulta tan sensible reflexionar sobre la neuroética? Porque se ocupa del cerebro, órgano<br />
responsable de nuestras percepciones, de nuestros pensamientos y de nuestra conciencia, y el conocimiento y/o su<br />
manipulación involucran a lo más genuino e intransferible del ser humano. Desde 2002, la neuroética ha sido considerada<br />
como nueva disciplina que ofrece un campo de reflexión para el conocimiento y las acciones neurocientíficas en lo que atañe a<br />
las personas como individuos y a la sociedad como organización.<br />
Dentro de este marco podemos distinguir dos ramas: la neuroética fundamental y la neuroética aplicada. La neuroética exige<br />
estar alertas y ofrecer ámbitos de encuentros interdisciplinarios donde participe la sociedad, propender a las reflexiones<br />
éticas e inclusive trabajar con anticipación los dilemas que están emergiendo. La ciencia no se detiene ni retrocede y su<br />
desarrollo ha adquirido un ritmo acelerado; por lo que no ha habido suficiente tiempo para debatir estos procesos. Estamos<br />
convencidos que la Neuroética será al siglo XXI, lo que la Genética fue al siglo XX.]]></dcterms:abstract>
    <dcterms:tableOfContents><![CDATA[The term neuroethics defines the bioethics field that deals with the dilemmas arising from the development of the neurosciences.<br />
Why are we so sensitive to ponder on neuroethics? Because it involves the brain, the organ responsible for our perceptions, our<br />
thoughts and our conscience; and its knowledge and/or manipulation entail the most genuine and nontransferable aspects of the<br />
human being.<br />
Since 2002, neuroethics has been recognized as a new discipline that offers an area of consideration for neuroscientific knowledge<br />
and the actions regarding human beings as individuals, and the society as an organization. Whitin its framework, we can distinguish<br />
two branches: fundamental neuroethics and applied neuroethics.<br />
Neuroethics demands that we are on alert, and we offer the possibility of interdisciplinary exchange programs, encouraging society<br />
to participate, promoting the ethical opinions, and even working with anticipation on the dilemmas that are already emerging. Science<br />
does not stop, and its development has acquired such an accelerated pace that there has not been enough time to discuss its<br />
processes.<br />
We are convinced that neuroethics will be for the 21st century, what genetics was for the 20th century.]]></dcterms:tableOfContents>
    <dcterms:creator><![CDATA[Alejandra T. Rabadán]]></dcterms:creator>
    <dcterms:publisher><![CDATA[Álvaro Campero]]></dcterms:publisher>
    <dcterms:date><![CDATA[Septiembre 2019]]></dcterms:date>
    <dcterms:dateAccepted><![CDATA[Junio 2019]]></dcterms:dateAccepted>
    <dcterms:dateSubmitted><![CDATA[Junio 2019]]></dcterms:dateSubmitted>
    <dcterms:rights><![CDATA[Asociación Argentina de Neurocirugía]]></dcterms:rights>
    <dcterms:references><![CDATA[1. Cabrera LY, Evans EL, Hamilton RH. Ethics of the Electrified Mind:<br />
Defining Issues and Perspectives on the Principled Use of Brain Stimulation<br />
in Medical Research and Clinical Care. Brain Topogr. 2014; 27(1):33-45.<br />
2. Cabrera LY. How does enhancing cognition affect human values? How<br />
does this translate into social responsibility? Curr Top Behav Neurosci.<br />
2015;19:223-41.<br />
3. Canavero S. HEAVEN: The head anastomosis venture Project outline for<br />
the first human head transplantation with spinal linkage (GEMINI). Surg<br />
Neurol Int 2013; 4:S335-42. Available FREE in open access from: http://<br />
surgicalneurologyint.com/text.asp?2013/4/2/335/1113444.<br />
4. Gorga M. Implicaciones éticas del conocimiento acerca del cerebro. Una<br />
aproximación a la neuroética. Revista Colombiana de Bioética, 2012; 7:1,<br />
123-139.<br />
5. Hayempour BJ. Psychosurgery: Treating Neurobiological Disorders with<br />
Neurosurgical Intervention. J Neurol Disord. 2013; 19;1(1).<br />
6. Iuculano T, Cohen Kadosh R. The mental cost of cognitive enhancement. J<br />
Neurosci. 2013; 6;33(10):4482-6.<br />
7. Northoff G. What is neuroethics? Empirical and theoretical neuroethics.<br />
Curr Opin Psychiatry. 2009; 22(6):565-9.<br />
8. Olesen J, Gustavsson A, Svensson M, Wittchen HU, Jönsson B;<br />
CDBE2010 study group; European Brain Council. The economic cost of<br />
brain disorders in Europe. Eur J Neurol. 2012 ; 19(1):155-62.<br />
9. Rabadán AT. Neuroética y Salud Pública. Trabajo Final para el Programa<br />
de Educación Permanente en Bioética. Introducción a la Bioética Clínica y<br />
Social. Red Bioética UNESCO. 2009 .<br />
10. Rabadán AT. http://ppct.caicyt.gov.ar/index.php/bcaeem/.<br />
11. Shaw D. Neuroenhancing public health. J Med Ethics. 2013; 21.<br />
12. The Dana Foundation. Neuroethics: Mapping the Field. Cerebrum. http://<br />
dana.org/Cerebrum/2002/Neuroethics__Mapping_the_Field/.<br />
13. Wardrope A. Authenticity and autonomy in deep-brain stimulation. J Med<br />
Ethics. 2014; 40(8):563-6.<br />
14. Rabadán AT. Neuroethics scope at a glance. Surg Neurol Int 2015; 6: 183.<br />
doi:10.4103/2152-7806.171249.]]></dcterms:references>
    <dcterms:language><![CDATA[Español]]></dcterms:language>
</rdf:Description></rdf:RDF>
