Tumores cerebrales en el programa de cirugía de la epilepsia del Centro Internacional de Restauración Neurológica (La Habana) / Brain tumors in the epilepsy surgery program of International Center for Neurological Restoration (La Habana)

Objetivo: Determinar la asociación de los tumores cerebrales con otras lesiones en los pacientes sometidos a cirugía de epilepsia en el Centro Internacional de Restauración Neurológica (CIREN La Habana,Cuba), así como el impacto en la evolución clínica posterior a la resección guiada por electrocorticografía (ECoG).Métodos: De los 47 pacientes con epilepsia farmacorresistente operados en el CIREN, se realizó un estudio descriptivo de aquellos con diagnóstico confirmado de tumor cerebral. Se efectuaron resecciones guiadas por ECoG y el diagnóstico histopatológico se realizó según la clasificación de la Organización Mundial de la Salud. Para el diagnóstico microscópico de displasia cortical focal se utilizó el sistemapropuesto por la Liga Internacional contra la Epilepsia. La escala de Engel modificada fue aplicada para el seguimiento postquirúrgico.Resultados: El promedio de edad previo a la cirugía fue de 32,8 años (5-19 años) y la duración promedio de la epilepsia fue de 21,5 años (2-42 años). El análisis histológico confirmó la presencia de tumor en 6 pacientes (3 gangliogliomas, 2 astrocitomas pilocíticos y 1 tumor neuroepitelial disembrioplásico); 4 correspondieron al lóbulo temporal y 2 extratemporales y de ellos, 3 estuvieron asociados a displasia cortical focal. La evolución postquirúrgica fue satisfactoria, estando libres de crisis en su última evaluación, 5 pacientes (rango de 7 y 9 años, estadios Ia, Ib y Ic). La paciente restante logró una reducción considerable de las crisis (5 años y medio de operada con un estadio IIIa).Conclusiones: La resección del tumor guiada por ECoG permite diagnosticar otras lesiones no identificadas en las resonancias magnéticas en el 50 Por ciento de los casos y cuya epileptogenicidad ha sido demostrada. La evolución clínica favorable en la mayoría de los pacientes sugiere la utilidad de la ECoG intraoperatoria para la adecuada resección de la zona epileptogénica(AU)

OBJECTIVE: To determine the association of brain tumors with other lesions in patients undergoing epilepsy surgery at the International Center for Neurological Restoration (CIREN –Havana, Cuba), as well as the impact on clinical evolution following the resection guided by electrocorticography (ECoG).METHODS: Of the 47 patients with epilepsy operated in the CIREN, a descriptive study was conducted of those with confirmed diagnosisof brain tumor. Resections guided by ECoG were carried out and the histopathological diagnosis was carried out according to the classification of the World Health Organization. The system proposed by the International League against Epilepsy was used for themicroscopic diagnosis of focal cortical dysplasia. The modified Engel scale was applied for post-surgical follow-up.RESULTS: The average age prior to surgery was 32.8 years (5-19 years) and the mean duration of epilepsy was 21.5 years (2-42 years).Histological analysis confirmed the presence of tumor in 6 patients (3 Gangliogliomas, 2 pilocytic astrocytomas and 1 dysembryoplasticneuroepithelial tumor); 4 corresponded to the temporal lobe and 2 extratemporals and of them, 3 were associated with focal cortical dysplasia. The postsurgical evolution was satisfactory, being free of seizures in its last evaluation, 5 patients (range of 7 and 9 years, grades Ia, Ib and Ic). The remaining patient achieved a considerable reduction in seizures (5 and half years of surgery with a grade IIIa).CONCLUSIONS: The resection of the tumor guided by ECoG allows diagnosing other unidentified lesions in the magnetic resonances in 50 Per cent of the cases and whose epileptogenicity has been demonstrated. Favorable clinical evolution in most patients suggests the usefulness of intraoperative ECoG for the adequate resection of the epileptogenic zone(AU)

Cuerpos amiláceos en la neocorteza de pacientes con epilepsia del lóbulo temporal y displasia cortical focal / Corpora amylacea in the neocortex in patients with temporal lobe epilepsy and focal cortical dysplasia

Introducción: Los cuerpos amiláceos (CoA) se presentan en aproximadamente el 60% de los hipocampos atróficos resecados de pacientes con epilepsia del lóbulo temporal farmacorresistente (ELTFR). Su presencia en la neocorteza temporal lateral ha sido observada con menor frecuencia. Objetivo: El objetivo es evaluar la presencia, la distribución y la densidad de CoA en el lóbulo temporal lateral de pacientes con ELTFR y displasia cortical focal (DCF) y la relación de su densidad con variables demográficas y clínicas. Métodos: Analizamos histológicamente el tejido resecado de 35 pacientes con ELTFR. La densidad de los CoA fue evaluada con una escala semicuantitativa según los criterios de Cherian et al. Resultados: La presencia de CoA en la neocorteza de 9 pacientes estuvo asociada a esclerosis hipocampal (DCF tipo IIIa, 7 casos), tumor neuroepitelial disembrioplásico (DCF tipo IIIb, un caso) y angioma cavernoso (DCF tipo IIIc, un caso). Todos los pacientes tuvieron afectación de la superficie meníngea (SM) y en 8 casos se localizaron en el parénquima cerebral (sustancia blanca) y alrededor de los vasos sanguíneos. La densidad de los CoA en SM tuvo una correlación negativa con la edad de inicio de las crisis (r = -0,828, p < 0,05) y positiva con la duración de la enfermedad (r = 0,678, p < 0,05) pero no con la evolución clínica postquirúrgica. Conclusiones: En pacientes con ELTFR con lesión principal (EH, tumor, malformación vascular) asociada a DCF ligeras se constata la acumulación de CoA en la neocorteza. No se encontró una asociación entre la presencia de CoA y la evolución clínica al año de la cirugía

Introduction: Corpora amylacea (CoA) are present in about 60% of atrophic hippocampi resected from patients with drug resistant temporal lobe epilepsy (DRTLE). They have also been described in the lateral temporal neocortex, although less frequently. Objective: The objective is to measure the presence, distribution and density of CoA in the lateral temporal lobes of patients with DRTLE and focal cortical dysplasia (FCD), also examining how CoA density may be linked to demographic and clinical traits. Methods: Resected tissue from 35 patients was analysed. CoA density was assessed with a semi-quantitative scale according to the criteria established by Cherian et al. Results: Presence of CoA in the neocortex of 9 patients was associated with hippocampal sclerosis (FCD type IIIa, 7 cases), disembryoplastic neuroepithelial tumour (FCD type IIIb, 1 case), and cavernous angioma (FCD type IIIc, 1 case). The meningeal surface (MS) was involved in all cases, and 8 cases displayed CoA in the cerebral parenchyma (white matter) and around blood vessels. CoA density on the MS showed a negative correlation with age at seizure onset (r = -0.828, P < .05) and a positive correlation with disease duration (r = 0.678, P < .05) but not with postoperative clinical outcome. Conclusions: Patients with DRTLE and a primary lesion (hippocampal sclerosis, tumour, vascular malformation) associated with mild FCD were shown to have CoA deposits in the neocortex. No association was found between presence of CoA and clinical outcome one year after surgery

Corpora amylacea in the neocortex in patients with temporal lobe epilepsy and focal cortical dysplasia.

INTRODUCTION: Corpora amylacea (CoA) are present in about 60% of atrophic hippocampi resected from patients with drug resistant temporal lobe epilepsy (DRTLE). They have also been described in the lateral temporal neocortex, although less frequently. OBJECTIVE: The objective is to measure the presence, distribution and density of CoA in the lateral temporal lobes of patients with DRTLE and focal cortical dysplasia (FCD), also examining how CoA density may be linked to demographic and clinical traits. METHODS: Resected tissue from 35 patients was analysed. CoA density was assessed with a semi-quantitative scale according to the criteria established by Cherian et al. RESULTS: Presence of CoA in the neocortex of 9 patients was associated with hippocampal sclerosis (FCD type iiia, 7 cases), disembryoplastic neuroepithelial tumour (FCD type iiib, 1 case), and cavernous angioma (FCD type iiic, 1 case). The meningeal surface (MS) was involved in all cases, and 8 cases displayed CoA in the cerebral parenchyma (white matter) and around blood vessels. CoA density on the MS showed a negative correlation with age at seizure onset (r = -0.828, P<.05) and a positive correlation with disease duration (r = 0.678, P<.05) but not with postoperative clinical outcome. CONCLUSIONS: Patients with DRTLE and a primary lesion (hippocampal sclerosis, tumour, vascular malformation) associated with mild FCD were shown to have CoA deposits in the neocortex. No association was found between presence of CoA and clinical outcome one year after surgery.

Microscopic mild focal cortical dysplasia in temporal lobe dual pathology: an electrocorticography study.

BACKGROUND: Associations between electrophysiological and histological findings might provide an insight into the epileptogenicity of mild focal cortical dysplasia (FCD) in patients with temporal lobe epilepsy (TLE) and a dual pathology. SUBJECTS AND METHODS: A total of 22 patients with pharmacoresistant TLE were included in the study, 16 of them with histologically confirmed hippocampal sclerosis (HS) associated with neocortical temporal mild Palmini Type-I FCD subtypes and 6 with HS. Intraoperative electrocorticography (ECoG) recordings were analysed for epileptiform discharge frequency and morphology. Associations between histological, and electrocorticography pattern findings in these patients were analysed. Electroclinical outcomes in these patients were also evaluated. RESULTS: Neocortical areas with mild Palmini Type-I FCD showed a significantly higher spike frequency (SF) recorded in the inferior temporal gyrus than those neocortical areas in patients with HS. There was a tendency to higher spike frequency and lower amplitude in neocortical areas with histopathologic subtype IB FCD in relation with IA during intraoperative ECoG. Post-SF excision and amplitude were significantly lower during neocortical post-excision intraoperative ECoG than during neocortical pre-excision recording. There was no difference found in the clinical outcome between patients with and without FCD. CONCLUSIONS: Intraoperative electrocorticographic interictal spike frequency recorded in the neocortical inferior temporal gyrus may help to characterize the histopathologic subtypes of mild Palmini Type-I FCD in patients with temporal lobe epilepsy (TLE) and a dual pathology. Our data support the epileptogenicity of neocortical mild FCD in TLE and assessments of ECoG patterns are relevant to determine the extent of the resection in these patients which can influence the electroclinical outcome.

Muerte neuronal en la neocorteza de pacientes con epilepsia del lóbulo temporal resistente a fármacos / Neuronal death in the neocortex of drug resistant temporal lobe epilepsy patients

Introducción. La participación de mecanismos de muerteapoptótica en la epilepsia del lóbulo temporal resistente afármacos (ELTRF) es un aspecto muy discutido en la actualidad.Investigamos si existe pérdida neuronal y la inmunodeteccióna diferentes marcadores de muerte en tejido neocorticalen ocho pacientes con ELTRF y como tejido controlse evaluaron cinco neocortezas de sujetos fallecidos porcausas no neurológicas, pareados en edad y sexo.Métodos. La evaluación de la pérdida neuronal se realizópor medio de un estudio estereológico y por técnica inmunohistoquímicacon el marcador sinaptofisina. Se evaluóla inmunopositividad a diferentes marcadores apoptóticos(anexina V, caspasa 3 y 8, bcl-2 y p53), así como la detecciónde fragmentación del ácido desoxirribonucleico (ADN) (TUNEL),y se realizó en todos los casos un doble marcaje con sinaptofisina.Los resultados fueron evaluados por microscopiaconfocal y analizados por el programa Zeiss LSM 5 ImageBrowser, 2.80.1113 (Alemania).Resultados. Se observó una disminución estadísticamentesignificativa del número total de células (p<0,05), asícomo de las células sinaptofisina+ (p<0,01) en la neocorteza(capa IV) de los pacientes con ELTRF al ser comparadoscon el tejido control. No mostraron diferencias significativaslos marcadores apoptóticos bcl-2, p53, caspasa 3 y 8 paraninguna de las capas de neocorteza, mientras que sí resultóestadísticamente aumentado el número de células TUNEL+(p<0,05) y anexina V+ (p<0,05) en la capa IV neocortical delos pacientes.Conclusiones. Este grupo de evidencias hablan a favorde la existencia en la capa IV de neocorteza de una afectaciónen el número neuronal que se puede asociar a un procesode muerte apoptótica por una vía no dependiente de caspasas,sin que pueda ser descartada la muerte por necrosis (AU)

Introduction. Participation of apoptotic death mechanisms in drug resistant temporal lobe epilepsy (DRTLE) is currently under great debate. We have investigated if there is neuronal loss and the immunodetection to differentmarkers in neocortical tissue death in eigth patients with DRTLE. The neocortexes of five patients deceased due to non-neurological causes, paired in age and gender were evaluated as control tissue. Methods. The evaluation of neuronal loss was made by means of a stereological study and with immunohisto chemical techniques with the synaptophysin marker. Immunopositivity to different apoptotic markers (annexin V, caspase 3 and 8, bcl-2 and p53) and detection of deoxyribonucleic acid (DNA) fragmentation (TUNEL) wereanalyzed and double labeling with synaptophysin was performed in every case. The results were evaluated with confocal microscope and analyzed with the Zeiss LSM 5 Image Browser Program, 2.80.1113 (Germany). Results. A statistically significant decrease in the total number of cells (p < 0.05) and the synaptophysin cells+ (p<0.01) in the neocortex (layer IV) of the patients with DRTLE when compared with the control tissue was found. No significant differences were found in the apoptotic markers bcl-2, p53, caspase 3 and 8 for any of the neocortex layers while there was a statistically significantincrease in the number of TUNEL cells+ (p<0.05) and annexin V+ (p<0.05) in the neocortical layer IV of the patients. Conclusions. This group of evidence speaks in favor of the existence of an effect on the neuronal number in the neocortex layer IV that may be associated with non caspase dependent apoptotic death process, without beingable to rule out death by necrosis

[Pathological neocortical findings in patients with medication-resistant medial temporal lobe epilepsy submitted to surgery]. / Hallazgos patológicos neocorticales en pacientes con epilepsia del lóbulo temporal medial farmacorresistente sometidos a cirugía.

INTRODUCTION: The dual pathology consisting of hippocampal sclerosis plus focal cortical dysplasia (FCD) is often reported in patients with medication-resistant medial temporal lobe epilepsy (MTLE). AIMS: To determine the histopathological changes that take place in the neocortex of patients with medication-resistant MTLE submitted to surgery and to evaluate the relation between the histopathological changes, pathological background and the clinical course of patients who had received surgical treatment. MATERIALS AND METHODS: Tissue obtained by en bloc resection from the neocortex of 18 patients with MTLE refractory to medical treatment was processed histologically and a tailored temporal lobectomy was performed with electrocorticography. RESULTS: Dual pathology was diagnosed in 13 patients (72.2%). Imaging studies confirmed the existence of mesial sclerosis of the temporal in 100% of cases and there was no evidence of neocortical lesions. Histologically, 46.15% and 38.46% of the patients were diagnosed as belonging to FCD type 1a and FCD type 1b, respectively. Only one patient presented FCD type 2a. A statistically significant relation was found between the presence of dual pathology and the existence of an early precipitating injury (p = 0.04). One year after surgery, 72.7% (8/11) patients with dual pathology were classified as belonging to Engel class I. CONCLUSIONS: In patients with MTLE there are microscopic FCD-type alterations in the neocortex. There is an association between these alterations and the existence of an initial precipitating injury. Complete resection of the epileptogenic area, which is guaranteed by the lobectomy tailored by electrocorticography, allows patients to enjoy a favourable post-surgical progression one year after surgery.

[Neuronal death in the neocortex of drug resistant temporal lobe epilepsy patients]. / Muerte neuronal en la neocorteza de pacientes con epilepsia del lóbulo temporal resistente a fármacos.

Introduction. Participation of apoptotic death mechanisms in drug resistant temporal lobe epilepsy (DRTLE) is currently under great debate. We have investigated if there is neuronal loss and the immunodetection to different markers in neocortical tissue death in eigth patients with DRTLE. The neocortexes of five patients deceased due to non-neurological causes, paired in age and gender were evaluated as control tissue. Methods. The evaluation of neuronal loss was made by means of a stereological study and with immunohistochemical techniques with the synaptophysin marker. Immunopositivity to different apoptotic markers (annexin V, caspase 3 and 8, bcl-2 and p53) and detection of deoxyribonucleic acid (DNA) fragmentation (TUNEL) were analyzed and double labeling with synaptophysin was performed in every case. The results were evaluated with confocal microscope and analyzed with the Zeiss LSM 5 Image Browser Program, 2.80.1113 (Germany). Results. A statistically significant decrease in the total number of cells (p < 0.05) and the synaptophysin cells+ (p<0.01) in the neocortex (layer IV) of the patients with DRTLE when compared with the control tissue was found. No significant differences were found in the apoptotic markers bcl-2, p53, caspase 3 and 8 for any of the neocortex layers while there was a statistically significant increase in the number of TUNEL cells+ (p<0.05) and annexin V+ (p<0.05) in the neocortical layer IV of the patients. Conclusions. This group of evidence speaks in favor of the existence of an effect on the neuronal number in the neocortex layer IV that may be associated with noncaspase dependent apoptotic death process, without being able to rule out death by necrosis. Key words: Drug resistant temporal lobe epilepsy. Apoptosis. Necrosis. Neuronal loss. Neurología 2008;23(9):555-565.

Hallazgos patológicos neocorticales en pacientes con epilepsia del lóbulo temporal medial farmacorresistente sometidos a cirugía / Pathological neocortical findings in patients with medication-resistant medial temporal lobe epilepsy submitted to surgery

Introducción. La patología dual compuesta por esclerosis hipocampal y displasia cortical focal (DCF) se describecon frecuencia en pacientes con epilepsia del lóbulo temporal medial (ELTM) farmacorresistente. Objetivos. Determinar los cambios histopatológicos en la neocorteza de pacientes con ELTM farmacorresistente sometidos a cirugía y evaluar la relación entre los cambios histopatológicos, los antecedentes patológicos y la evolución clínica en los pacientes operados. Materialesy métodos. Se procesó histológicamente el tejido resecado en bloque (neocorteza) de 18 pacientes con ELTM refractaria a tratamiento médico, y se les realizó lobectomía temporal ajustada por electrocorticografía. Resultados. Se diagnóstico patología dual en 13 pacientes (72,2por ciento). Los estudios imagenológicos confirmaron en el 100por ciento de los casos la esclerosis mesial del temporal y no existieron evidencias de lesión neocortical. Histológicamente, el 46,15 por ciento y el 38,46 por ciento de los pacientesfueron diagnosticados como DCF tipo 1a y DCF tipo 1b, respectivamente. Sólo un paciente presentó DCF tipo 2a. Se demostró una relación estadísticamente significativa entre la presencia de patología dual y la existencia de una daño precipitante inicial (p = 0,04). El 72,7por ciento (8/11) de los pacientes con patología dual un año después de la cirugía se clasificó en la clase Ide Engel. Conclusiones. En los pacientes con ELTM existen alteraciones microscópicas en la neocorteza del tipo DCF. Estas alteraciones se asocian a la existencia de un daño precipitante inicial. La resección completa de la zona epileptogénica, garantizada por la lobectomía ajustada por electrocorticografía, permite una buena evolución posquirúrgica un año después de la cirugía(AU)

INTRODUCTION: The dual pathology consisting of hippocampal sclerosis plus focal cortical dysplasia (FCD) is often reported in patients with medication-resistant medial temporal lobe epilepsy (MTLE). AIMS: To determine the histopathological changes that take place in the neocortex of patients with medication-resistant MTLE submitted to surgery and to evaluate the relation between the histopathological changes, pathological background and the clinical course of patients who had received surgical treatment. MATERIALS AND METHODS: Tissue obtained by en bloc resection from the neocortex of 18 patients with MTLE refractory to medical treatment was processed histologically and a tailored temporal lobectomy was performed with electrocorticography. RESULTS: Dual pathology was diagnosed in 13 patients (72.2percent). Imaging studies confirmed the existence of mesial sclerosis of the temporal in 100 percent of cases and there was no evidence of neocortical lesions. Histologically, 46.15 percent and 38.46 percent of the patients were diagnosed as belonging to FCD type 1a and FCD type 1b, respectively. Only one patient presented FCD type 2a. A statistically significant relation was found between the presence of dual pathology and the existence of an early precipitating injury (p = 0.04). One year after surgery, 72.7percent (8/11) patients with dual pathology were classified as belonging to Engel class I. CONCLUSIONS: In patients with MTLE there are microscopic FCD-type alterations in the neocortex. There is an association between these alterations and the existence of an initial precipitating injury. Complete resection of the epileptogenic area, which is guaranteed by the lobectomy tailored by electrocorticography, allows patients to enjoy a favourable post-surgical progression one year after surgery(AU)

Hallazgos patológicos neocorticales en pacientes con epilepsia del lóbulo temporal medial farmacorresistente sometidos a cirugía / Pathological neocortical findings in patients with medication-resistant medial temporal lobe epilepsy submitted to surgery

La patología dual compuesta por esclerosis hipocampal y displasia cortical focal (DCF) se describecon frecuencia en pacientes con epilepsia del lóbulo temporal medial (ELTM) farmacorresistente. Objetivos. Determinar los cambios histopatológicos en la neocorteza de pacientes con ELTM farmacorresistente sometidos a cirugía y evaluar la relación entre los cambios histopatológicos, los antecedentes patológicos y la evolución clínica en los pacientes operados. Materialesy métodos. Se procesó histológicamente el tejido resecado en bloque (neocorteza) de 18 pacientes con ELTM refractaria a tratamiento médico, y se les realizó lobectomía temporal ajustada por electrocorticografía. Resultados. Se diagnóstico patología dual en 13 pacientes (72,2%). Los estudios imagenológicos confirmaron en el 100% de los casos la esclerosis mesialdel temporal y no existieron evidencias de lesión neocortical. Histológicamente, el 46,15% y el 38,46% de los pacientes fueron diagnosticados como DCF tipo 1a y DCF tipo 1b, respectivamente. Sólo un paciente presentó DCF tipo 2a. Se demostró una relación estadísticamente significativa entre la presencia de patología dual y la existencia de una daño precipitante inicial (p = 0,04). El 72,7% (8/11) de los pacientes con patología dual un año después de la cirugía se clasificó en la clase Ide Engel. Conclusiones. En los pacientes con ELTM existen alteraciones microscópicas en la neocorteza del tipo DCF. Estas alteraciones se asocian a la existencia de un daño precipitante inicial. La resección completa de la zona epileptogénica, garantizadapor la lobectomía ajustada por electrocorticografía, permite una buena evolución posquirúrgica un año después de la cirugía

The dual pathology consisting of hippocampal sclerosis plus focal cortical dysplasia (FCD) is oftenreported in patients with medication-resistant medial temporal lobe epilepsy (MTLE). Aims. To determine the histopathological changes that take place in the neocortex of patients with medication-resistant MTLE submitted to surgery and to evaluate the relation between the histopathological changes, pathological background and the clinical course of patients whohad received surgical treatment. Materials and methods. Tissue obtained by en bloc resection from the neocortex of 18 patients with MTLE refractory to medical treatment was processed histologically and a tailored temporal lobectomy was performed with electrocorticography. Results. Dual pathology was diagnosed in 13 patients (72.2%). Imaging studies confirmed the existenceof mesial sclerosis of the temporal in 100% of cases and there was no evidence of neocortical lesions. Histologically, 46.15% and 38.46% of the patients were diagnosed as belonging to FCD type 1a and FCD type 1b, respectively. Only one patient presented FCD type 2a. A statistically significant relation was found between the presence of dual pathology and the existenceof an early precipitating injury (p = 0.04). One year after surgery, 72.7% (8/11) patients with dual pathology were classified as belonging to Engel class I. Conclusions. In patients with MTLE there are microscopic FCD-type alterations in the neocortex.There is an association between these alterations and the existence of an initial precipitating injury. Complete resection of the epileptogenic area, which is guaranteed by the lobectomy tailored by electrocorticography, allows patients to enjoy a favourable post-surgical progression one year after surgery

[Video-EEG evaluation complemented by spectral and EEG source analysis in patients with medication-resistant medial temporal lobe epilepsy]. / Evaluación videoelectroencefalográfica complementada con análisis espectral y de las fuentes generadoras del electroencefalograma en pacientes con epilepsia del lóbulo temporal medial resistente a los fármacos.

AIM: To evaluate the value of prolonged video-electroencephalographic (video-EEG) monitoring complemented with spectral and EEG source analysis in identifying the epileptogenic area in patients with medial temporal lobe epilepsy who are candidates for non-lesional resective surgery. PATIENTS AND METHODS: The electrographic patterns during the onset of seizures were evaluated in over 667 seizures from 41 patients with a clinical diagnosis of medication-resistant partial epilepsy. Analyses were performed using Harmonie software and variable resolution electrical tomography (VARETA). RESULTS: Video-EEG was used to determine that 53.6% of the patients evaluated suffered complex partial seizures of a temporal origin; these were characterised by having an average frequency of 5.56 +/- 1.56 Hz, while the non-temporal seizures displayed a frequency within the range 9.17 +/- 3.32 Hz. The topographic location of the dominant ictal frequency during the period of maximum spectral energy in patients with temporal lobe epilepsy enabled us to draw a distinction between a group of patients with mesial seizures and those with non-mesial seizures that exceeded the number that was determined by visual inspection of the EEG, that is, 78.9 versus 47.3%, respectively. There was a 100% coincidence between the area where the seizures began as defined by surface EEG complemented with spectral analysis, the generator of this activity as defined by VARETA and the epileptogenic region. CONCLUSIONS: The localising information provided by video-EEG complemented with spectral and EEG source analysis allows for non-invasive location of the epileptogenic region in patients with medial temporal lobe epilepsy even when structural imaging studies show an absence or bilaterality of abnormalities.

Evaluación videoelectroencefalográfica complementada con análisis espectral y de las fuentes generadoras del electroencefalograma en pacientes con epilepsia del lóbulo temporal medial resistente a los fármacos / Video-EEG evaluation complemented by spectral and EEG source analysis in patients with medication-resistant medial temporal lobe epilepsy

Objetivo. Evaluar la contribución de la monitorización prolongada videoelectroencefalográfica (video EEG) complementada con análisis espectral y de las fuentes generadoras del electroencefalograma (EEG) en la identificación de la zona epileptogénica de pacientes con epilepsia del lóbulo temporal medial candidatos a cirugía resectiva no lesional. Pacientesy métodos. Se evaluaron los patrones electrográficos del inicio ictal en más de 667 crisis correspondientes a 41 pacientes con diagnóstico clínico de epilepsia parcial resistente a fármacos. Para el análisis se utilizaron el software Harmonie y la tomografía eléctrica de resolución variable (VARETA). Resultados. Mediante video-EEG se determinó que el 53,6por ciento de lospacientes evaluados presentaba crisis parciales complejas de origen temporal; éstas se caracterizaron por una frecuencia media de 5,56 ± 1,56 Hz, mientras que las no temporales presentaron una frecuencia en el rango de 9,17 ± 3,32 Hz. La localizacióntopográfica de la frecuencia ictal dominante durante el período de energía espectral máxima en los pacientes conepilepsia del lóbulo temporal permitió distinguir a un grupo de pacientes con crisis mesiales y otros no mesiales que superaron el número determinado por la inspección visual del EEG: un 78,9 frente a un 47,3por ciento, respectivamente. Se evidenció unacoincidencia del 100por ciento entre la zona de inicio ictal definida por EEG de superficie complementada con análisis espectral, el generador de esta actividad definido por VARETA y la zona epileptogénica. Conclusiones. La información localizadora aportadapor el video-EEG complementada con el análisis espectral y de las fuentes del EEG permite localizar de forma no invasiva la zona epileptogénica en pacientes con epilepsia del lóbulo temporal medial aun cuando los estudios imaginológicos estructurales evidencian ausencia o bilateralidad de anomalías(AU)

Summary. Aim. To evaluate the value of prolonged video electroencephalographic (video-EEG) monitoring complemented with spectral and EEG source analysis in identifying the epileptogenic area in patients with medial temporal lobe epilepsy who are candidates for non-lesional resective surgery. Patients and methods. The electrographic patterns during the onset of seizures were evaluated in over 667 seizures from 41 patients with a clinical diagnosis of medication-resistant partial epilepsy. Analyses were performed using Harmonie software and variable resolution electrical tomography (VARETA). Results. Video- EEG was used to determine that 53.6percent of the patients evaluated suffered complex partial seizures of a temporal origin; these were characterised by having an average frequency of 5.56 ± 1.56 Hz, while the non-temporal seizures displayed a frequency within the range 9.17 ± 3.32 Hz. The topographic location of the dominant ictal frequency during the period of maximum spectral energy in patients with temporal lobe epilepsy enabled us to draw a distinction between a group of patients withmesial seizures and those with non-mesial seizures that exceeded the number that was determined by visual inspection of the EEG, that is, 78.9 versus 47.3percent, respectively. There was a 100percent coincidence between the area where the seizures began asdefined by surface EEG complemented with spectral analysis, the generator of this activity as defined by VARETA and the epileptogenic region. Conclusions. The localising information provided by video-EEG complemented with spectral and EEG source analysis allows for non-invasive location of the epileptogenic region in patients with medial temporal lobe epilepsy even when structural imaging studies show an absence or bilaterality of abnormalities(AU)

Evaluación videoelectroencefalográfica complementada con análisis espectral y de las fuentes generadoras del electroencefalograma en pacientes con epilepsia del lóbulo temporal medial resistente a los fármacos / Video-EEG evaluation complemented by spectral and EEG source analysis in patients with medication-resistant medal temporal lobe epilepsy

Objetivo. Evaluar la contribución de la monitorización prolongada videoelectroencefalográfica (video-EEG) complementada con análisis espectral y de las fuentes generadoras del electroencefalograma (EEG) en la identificación de la zona epileptogénica de pacientes con epilepsia del lóbulo temporal medial candidatos a cirugía resectiva no lesional. Pacientes y métodos. Se evaluaron los patrones electrográficos del inicio ictal en más de 667 crisis correspondientes a 41 pacientes con diagnóstico clínico de epilepsia parcial resistente a fármacos. Para el análisis se utilizaron el software Harmonie y la tomografía eléctrica de resolución variable (VARETA). Resultados. Mediante video-EEG se determinó que el 53,6% de los pacientes evaluados presentaba crisis parciales complejas de origen temporal; éstas se caracterizaron por una frecuencia media de 5,56 ± 1,56 Hz, mientras que las no temporales presentaron una frecuencia en el rango de 9,17 ± 3,32 Hz. La localización topográfica de la frecuencia ictal dominante durante el período de energía espectral máxima en los pacientes con epilepsia del lóbulo temporal permitió distinguir a un grupo de pacientes con crisis mesiales y otros no mesiales que superaron el número determinado por la inspección visual del EEG: un 78,9 frente a un 47,3%, respectivamente. Se evidenció una coincidencia del 100% entre la zona de inicio ictal definida por EEG de superficie complementada con análisis espectral, el generador de esta actividad definido por VARETA y la zona epileptogénica. Conclusiones. La información localizadora aportada por el video-EEG complementada con el análisis espectral y de las fuentes del EEG permite localizar de forma no invasiva la zona epileptogénica en pacientes con epilepsia del lóbulo temporal medial aun cuando los estudios imaginológicos estructurales evidencian ausencia o bilateralidad de anomalías

Aim. To evaluate the value of prolonged video-electroencephalographic (video-EEG) monitoring complemented with spectral and EEG source analysis in identifying the epileptogenic area in patients with medial temporal lobe epilepsy who are candidates for non-lesional resective surgery. Patients and methods. The electrographic patterns during the onset of seizures were evaluated in over 667 seizures from 41 patients with a clinical diagnosis of medication-resistant partial epilepsy. Analyses were performed using Harmonie software and variable resolution electrical tomography (VARETA). Results. Video- EEG was used to determine that 53.6% of the patients evaluated suffered complex partial seizures of a temporal origin; these were characterised by having an average frequency of 5.56 ± 1.56 Hz, while the non-temporal seizures displayed a frequency within the range 9.17 ± 3.32 Hz. The topographic location of the dominant ictal frequency during the period of maximum spectral energy in patients with temporal lobe epilepsy enabled us to draw a distinction between a group of patients with mesial seizures and those with non-mesial seizures that exceeded the number that was determined by visual inspection of the EEG, that is, 78.9 versus 47.3%, respectively. There was a 100% coincidence between the area where the seizures began as defined by surface EEG complemented with spectral analysis, the generator of this activity as defined by VARETA and the epileptogenic region. Conclusions. The localising information provided by video-EEG complemented with spectral and EEG source analysis allows for non-invasive location of the epileptogenic region in patients with medial temporal lobe epilepsy even when structural imaging studies show an absence or bilaterality of abnormalities

Paraganglioma de la cola de caballo: informe de un caso / Cauda equina paraganglioma: a case report

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[Penetrating head injury from harpoon. Case report]. / Trauma craneoencefálico perforante por arpón. Precentación de un caso y revisión de la literatura.

The harpoon presence as aggressor weapon is unusual in the neurosurgical practice. Most cases are associated with diving or sport activities as result of imprudence. A 31 year old patient who sustained a penetrating craniocerebral injury with a fishing harpoon is presented and complementary exams, neurosurgical procedure and postoperative evolution are detailed. We discuss the management of this unusual injury and review the current literature on craniocerebral injuries caused by similar objects.

[Presentation of distal saccular aneurysm as a subdural haematoma]. / Aneurisma sacular distal presentándose como hematoma subdural.

INTRODUCTION: Intracranial aneurysms are one of the most frequent vascular diseases. Nevertheless, saccular aneurysms that are not due to an inflammatory aetiology, which are located in the peripheral segment of the posterior circulation, are extremely rare. They are most frequently located in the thickest arterial branches within the region of the anterior brain circulation, as is the case of the complex made up of the anterior cerebral artery posterior communicating artery, middle cerebral artery and posterior communicating artery. No clinical manifestations are produced in many of these aneurysms, and their rupture and the subsequent development of a subarachnoid haemorrhage is the cause of the most intense neurological damage, which on occasions can lead to fatal consequences. CASE REPORT: We report the case of a patient who was a carrier of distal aneurysm, located in the posterior region of the brain circulation, and also the neuroradiological findings, the form of clinical presentation and surgical treatment carried out, which allowed us to identify and close the afferent vessel and the resection of the aneurysmatic sac. CONCLUSION: From the presentation of the symptoms of this patient in the form of a subarachnoid haemorrhage, accompanied by a subdural haematoma, it could be inferred that these clinical and imagenological findings point to the rupture of a distal aneurysm. Application of the stereotactic approach would be one of the first choice treatments for aneurysms in the distal region if we bear in mind the characteristics of the afferent vessel, the size of the neck and the morphology of the sac

Aneurisma sacular distal presentándosecomo hematoma subdural / Presentation of distal saccular aneurysm as a subdural haematoma

Introducción. Los aneurismas intracraneales constituyen una de las enfermedades vasculares, que se presentan con gran frecuencia. Sin embargo, aquellos aneurismas saculares que no son de una etiología inflamatoria, que se localizan en el segmento periférico de la circulación posterior, son extremadamente raros. Su localización más frecuente se encuentra en las ramas arteriales de mayor calibre en el territorio de la circulación cerebral anterior, como es el caso del complejo cerebral anterior-comunicante anterior, cerebral media y arteria comunicante posterior. Las manifestaciones clínicas en muchos de estos aneurismas no se producen, y su ruptura y en consecuencia el desarrollo de un cuadro de hemorragia subaracnoidea es la causa del daño neurológico más intenso, y llega en ocasiones a consecuencias fatales. Caso clínico. Informamos de un paciente portador de un aneurisma distal, situado en el territorio posterior de la circulación cerebral, así como los hallazgos neurorradiológicos, forma clínica de presentación y tratamiento quirúrgico realizado, con el cual se logró la identificación y cierre del vaso aferente y la resección del saco aneurismático. Conclusión. Por la presentación de los síntomas en esta paciente en forma de una hemorragia subaracnoidea, acompañada de un hematoma subdural, podría inferirse que estos hallazgos clínicos y radiológicos sugerirían la ruptura de un aneurisma distal. La aplicación del abordaje estereotáctico es uno de los tratamientos de elección para los aneurismas de territorio distal si se tienen en cuenta las características del vaso aferente, el tamaño del cuello y la morfología del saco (AU)

Trauma craneoencefálico perforante por arpón. Presentación de un caso y revisión de la literatura / Penetrating head injury from harpoon. Case report

La presencia de un arpón como agente agresor resulta poco común en la práctica neuroquirúrgica, no siendo reportados casos similares en amplias series. La mayoría de estos casos resultan de accidentes en el buceo o en actividades deportivas, en ambos casos como resultado de violaciones de las medidas de seguridad. Se presenta en este trabajo a un paciente de 31 años que accidentalmente sufre un trauma craneoencefálico perforante por un arpón, exponiéndose los exámenes complementarios realizados, detallándosela conducta neuroquirúrgica aplicada y su evolución postoperatoria. Se discute nuestra experiencia en el manejo de este inusual caso y se realiza un análisis y comparación con los casos reportados en la literatura (AU)

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