Epilepsies Associated With Hippocampal Sclerosis.


Autoria(s): Cendes, Fernando; Sakamoto, Americo C; Spreafico, Roberto; Bingaman, William; Becker, Albert J
Contribuinte(s)

UNIVERSIDADE DE ESTADUAL DE CAMPINAS

Data(s)

01/07/2014

27/11/2015

27/11/2015

Resumo

Hippocampal sclerosis (HS) is considered the most frequent neuropathological finding in patients with mesial temporal lobe epilepsy (MTLE). Hippocampal specimens of pharmacoresistant MTLE patients that underwent epilepsy surgery for seizure control reveal the characteristic pattern of segmental neuronal cell loss and concomitant astrogliosis. However, classification issues of hippocampal lesion patterns have been a matter of intense debate. International consensus classification has only recently provided significant progress for comparisons of neurosurgical and clinic-pathological series between different centers. The respective four-tiered classification system of the International League Against Epilepsy subdivides HS into three types and includes a term of gliosis only, no-HS. Future studies will be necessary to investigate whether each of these subtypes of HS may be related to different etiological factors or with postoperative memory and seizure outcome. Molecular studies have provided potential deeper insights into the pathogenesis of HS and MTLE on the basis of epilepsy-surgical hippocampal specimens and corresponding animal models. These include channelopathies, activation of NMDA receptors, and other conditions related to Ca(2+) influx into neurons, the imbalance of Ca(2+)-binding proteins, acquired channelopathies that increase neuronal excitability, paraneoplastic and non-paraneoplastic inflammatory events, and epigenetic regulation promoting or facilitating hippocampal epileptogenesis. Genetic predisposition for HS is clearly suggested by the high incidence of family history in patients with HS, and by familial MTLE with HS. So far, it is clear that HS is multifactorial and there is no individual pathogenic factor either necessary or sufficient to generate this intriguing histopathological condition. The obvious variety of pathogenetic combinations underlying HS may explain the multitude of clinical presentations, different responses to clinical and surgical treatment. We believe that the stratification of neuropathological patterns can help to characterize specific clinic-pathological entities and predict the postsurgical seizure control in an improved fashion.

128

21-37

Identificador

Acta Neuropathologica. v. 128, n. 1, p. 21-37, 2014-Jul.

1432-0533

10.1007/s00401-014-1292-0

http://www.ncbi.nlm.nih.gov/pubmed/24823761

http://repositorio.unicamp.br/jspui/handle/REPOSIP/201402

24823761

Idioma(s)

eng

Relação

Acta Neuropathologica

Acta Neuropathol.

Direitos

fechado

Fonte

PubMed

Palavras-Chave #Animals #Diagnosis, Differential #Epilepsy #Hippocampus #Humans #Tuberous Sclerosis
Tipo

Artigo de periódico