Improvement in hippocampal kindling analysis through computational processing data / Aprimorando a análise do modelo de kindling hipocampal com o auxílio de processamento computacional

The kindling phenomenon is classically investigated in epileptology research. The present study aims to provide further information about hippocampal kindling through computational processing data. Adult Wistar rats were implanted with dorsal hippocampal and frontal neocortical electrodes to perform the experiment. The processing data was obtained using the Spike2 and Matlab softwares. An inverse relationship between the number of "wet dog shakes" and the Racine's motor stages development was found. Moreover it was observed a significant increase in the afterdischarge (AD) duration and its frequency content. The highest frequencies were, however, only reached at the beginning of behavioral seizures. During the primary AD, fast transients (ripples) were registered in both hippocampi superimposed to slower waves. This experiment highlights the usefulness of computational processing applied to animal models of temporal lobe epilepsy and supports a relevant role of the high frequency discharges in temporal epileptogenesis.

O fenômeno de kindling é classicamente utilizado no campo da epileptologia experimental. Este trabalho objetiva aprofundar a análise do modelo kindling hipocampal através de processamento computacional. Ratos wistar adultos receberam eletrodos hipocampais dorsais e neocorticais frontais para a realização do experimento. O processamento dos dados encontrados foi realizado pelos softwares Matlab e Spike2. Encontrou-se uma relação inversa entre wet dog shakes e o desenvolvimento dos estágios motores de Racine. A duração e o conteúdo de freqüência das pós-descargas hipocampais aumentaram durante o processo, sendo observadas descargas de alta freqüência (ripples) em ambos os hipocampos durante as pós-descargas primárias, superimpostas a ondas lentas. As mais altas freqüências, entretanto, foram apenas atingidas com o início das crises epilépticas. A utilização de sistemas computacionais para a confecção e análise do modelo de epilepsia temporal é ressaltada e reforça-se a relevância do papel das altas freqüências na epileptogênese temporal.

Esclerose hipocampal unilateral com registro subdural de crises temporais contralaterais: relato de caso / Unilateral hippocampal sclerosis with subdural strips in seizures from the contralateral temporal lobe: case report

INTRODUÇÃO: Pacientes com epilepsia temporal e esclerose hipocampal unilateral tem, na sua grande maioria das vezes, as suas crises e as alterações eletroencefalográficas interictais originando-se do lado da lesão. Mesmo alguns pacientes nos quais os registros de escalpo mostram as crises originando-se da região temporal contralateral à atrofia do hipocampo, registros invasivos têm mostrado que a região de início das crises é, na realidade, ipsilateral à atrofia. No entanto isso talvez não seja verdadeiro para todos pacientes. OBJETIVO: Nesse artigo é relatado uma paciente com atrofia hipocampal unilateral, mas cujas crises, tanto no escalpo quando com registros subdurais, mostram vir da região temporal contralateral. RESULTADO: A paciente tem atrofia hipocampal à direita mas cujo EEG interictal mostrava predomínio de descargas à esquerda, bem como crises vindo daí. O registro com strips subdurais mostrou origem das crises à esquerda. CONCLUSÃO: Possivelmente alguns pacientes com epilepsia temporal têm as crises vindo do hipocampo menos atrófico.

INTRODUCTION: Most patients with temporal lobe epilepsy and hippocampal sclerosis have the seizures and the interictal electroencephalographic abnormalities coming from the side of atrophic hippocampus. Even some patients on whom the seizures seem to arise from the contralateral temporal lobe, invasive recordings have shown that the seizures actually come from that atrophic side. But this may not be always the case. OBJECTIVE: We report a patient with a unilateral hippocampal atrophy and the seizures, seen both on the scalp as well with subdural strips, come from the contralateral temporal lobe. A patient with right hippocampal atrophy had most of the interictal discharges coming from the left temporal lobe, as well her seizures. Invasive recordings with subdural strips also showed seizures arising from the left temporal lobe. CONCLUSION: There might be some patients with temporal lobe epilepsy whose seizures come from the less.

Multivariate Analysis of Influential Factors for Loss of Neuron in Ammonias by Detection of Proton Maganetic Resonance in Children with Temporal Epilepsy / 实用儿科临床杂志

2 years),seizure frequency(≥1 time/month),persistence time(≥60 s),gene-ralized seizure were all associated with the incidence of the loss of neuron in ammonias.Multivariate Logistic regression analysis showed that the independent influencital factors for the loss of neuron in ammonias in children with temporal epilepsy included seizure frequency,persis-tence time and tape of seizure. Conclusions The loss of neuron in ammonias though 1H-MRS can be detected.The results of multivariate analysis verify that the development of the loss of neuron in ammonias may be associated with many factors including age of onset,course of di-sease,seizure frequency,persistence time and generalized seizure.In order to lower the incidence of the loss of neuron,early intervening treatment is very important.

Surgery outcome of pediatric intractable temporal epilepsy / 医学研究生学报

Objective:To discuss the surgical outcome of pediatric intractable temporal epilepsy. Methods:This observation included 34 pediatric patients with intractable temporal epilepsy who were admitted to our hospital from 1990 to 2001.CT or MRI,EEG and neuropsychological examinations were taken to determine the situations of the patients.They all underwent improved anterior temporal lobectomy. Results:The patients have been followed up for 2-13 years.According to Engel's classification,the achieved outcomes were seizure-free in 22(65 %) patients,apparently improved in 3(9 %) patients,improved in 3(9 %) patients,no effect in 2(6 %) patients,and lost of follow-up in 4(12 %) patients,respectively. Conclusion:Surgical treatment to pediatric intractable temporal epilepsy is safe and effective.The most common pathological causes for pediatric epilepsy are tumor and hippocampus sclerosis.Early surgery of pediatric temporal epilepsy could improve the life qualities of patients.

Incidence and clinical profile of extra-medial-temporal epilepsy with hippocampal atrophy

We tried to investigate the incidence and the clinical profile of intractable epilepsy with hippocampal atrophy and ictal onset zones located in areas other than the hippocampus (extra-medial-temporal epilepsy; EMTE). We included patients who had hippocampal atrophy confirmed by MRI but with extra-medial-temporal ictal onset zones as verified by invasive intracranial electrodes or video-EEG monitoring. The case histories, interictal EEG, ictal semiology, other MRI findings in addition to hippocampal atrophy, and results of ictal SPECT and PET scans were evaluated. Results were compared with those of surgically proven medial temporal lobe epilepsy with hippocampal atrophy recruited during the same period. 8.5% of the intractable epilepsy patients with hippocampal atrophy had extra-medial temporal epileptogenic zones. A history of encephalitis and hemiconvulsion-hemiparesis were significantly common in the EMTE group. Most of the interictal EEGs of EMTE patients showed extratemporal irritative zones. MRI, ictal SPECT, and FDG-PET seemed to be helpful at localizing the true epileptogenic zones. The predominant EMTE seizure type was focal motor seizure with secondary generalization. Some portion of intractable epilepsy patients with hippocampal atrophy had extra-medial-temporal epileptogenic foci and careful analysis of semiology and neuroimagings could yield clues to correct diagnosis.