Clinic feature of the mesial temporal sclerosis in children
Autor(a) principal: | |
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Data de Publicação: | 2007 |
Outros Autores: | |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Journal of epilepsy and clinical neurophysiology (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-26492007000300005 |
Resumo: | INTRODUCTION: Mesial temporal sclerosis is not a frequent cause of refractory epilepsy in children, and the its start age is uncertain. OBJECTIVE: To understand the clinic feature of children with mesial temporal sclerosis diagnosis. MATERIAL AND METHODS: It was done a literature review about this pathology in children, and it has been found a group of 4 articles that allow a general view about mesial temporal sclerosis in children and other group of 7 articles (case reports or small series) in which mesial temporal sclerosis was diagnosed until five years old. RESULTS: It was evaluated in the first group, febrile seizure that was the most frequent antecedent followed by a status epilepticus and the semiology of the seizures was characterized by oroalimentary automatism, gestural automatism, stunted movement and motor phenomenon.The group of children with mesial temporal sclerosis until five years old stood out due to the high incidence of status epilepticus (84,6%), by the number of children with altered neuropsycomotor development (46%), and by lesion in most of bilateral cases (53,8%) , suggesting that the bilateral form of the mesial temporal sclerosis might be a distinct pathology, and not necessarily the progression of a unilateral beginning picture. Another important thing to stand out in this group is the documentation by MR in edema in hippocampus after a status epilepticus and posterior atrophy of this structure. CONCLUSION: mesial temporal sclerosis can to appear still in early life and in any cases can to present an evolutional character and dependent from a previous aggression to the hippocampus. |
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Clinic feature of the mesial temporal sclerosis in childrentemporal lobe epilepsychildadolescentsclerosishippocampusINTRODUCTION: Mesial temporal sclerosis is not a frequent cause of refractory epilepsy in children, and the its start age is uncertain. OBJECTIVE: To understand the clinic feature of children with mesial temporal sclerosis diagnosis. MATERIAL AND METHODS: It was done a literature review about this pathology in children, and it has been found a group of 4 articles that allow a general view about mesial temporal sclerosis in children and other group of 7 articles (case reports or small series) in which mesial temporal sclerosis was diagnosed until five years old. RESULTS: It was evaluated in the first group, febrile seizure that was the most frequent antecedent followed by a status epilepticus and the semiology of the seizures was characterized by oroalimentary automatism, gestural automatism, stunted movement and motor phenomenon.The group of children with mesial temporal sclerosis until five years old stood out due to the high incidence of status epilepticus (84,6%), by the number of children with altered neuropsycomotor development (46%), and by lesion in most of bilateral cases (53,8%) , suggesting that the bilateral form of the mesial temporal sclerosis might be a distinct pathology, and not necessarily the progression of a unilateral beginning picture. Another important thing to stand out in this group is the documentation by MR in edema in hippocampus after a status epilepticus and posterior atrophy of this structure. CONCLUSION: mesial temporal sclerosis can to appear still in early life and in any cases can to present an evolutional character and dependent from a previous aggression to the hippocampus.Liga Brasileira de Epilepsia (LBE)2007-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-26492007000300005Journal of Epilepsy and Clinical Neurophysiology v.13 n.3 2007reponame:Journal of epilepsy and clinical neurophysiology (Online)instname:Liga Brasileira de Epilepsia (LBE)instacron:LBE10.1590/S1676-26492007000300005info:eu-repo/semantics/openAccessBrandão,Eliana Maria DominguesManreza,Maria Luiza Giraldes deeng2007-12-07T00:00:00Zoai:scielo:S1676-26492007000300005Revistahttp://epilepsia.org.br/publicacoes/ONGhttps://old.scielo.br/oai/scielo-oai.php||jecnpoa@terra.com.br1980-53651676-2649opendoar:2007-12-07T00:00Journal of epilepsy and clinical neurophysiology (Online) - Liga Brasileira de Epilepsia (LBE)false |
dc.title.none.fl_str_mv |
Clinic feature of the mesial temporal sclerosis in children |
title |
Clinic feature of the mesial temporal sclerosis in children |
spellingShingle |
Clinic feature of the mesial temporal sclerosis in children Brandão,Eliana Maria Domingues temporal lobe epilepsy child adolescent sclerosis hippocampus |
title_short |
Clinic feature of the mesial temporal sclerosis in children |
title_full |
Clinic feature of the mesial temporal sclerosis in children |
title_fullStr |
Clinic feature of the mesial temporal sclerosis in children |
title_full_unstemmed |
Clinic feature of the mesial temporal sclerosis in children |
title_sort |
Clinic feature of the mesial temporal sclerosis in children |
author |
Brandão,Eliana Maria Domingues |
author_facet |
Brandão,Eliana Maria Domingues Manreza,Maria Luiza Giraldes de |
author_role |
author |
author2 |
Manreza,Maria Luiza Giraldes de |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Brandão,Eliana Maria Domingues Manreza,Maria Luiza Giraldes de |
dc.subject.por.fl_str_mv |
temporal lobe epilepsy child adolescent sclerosis hippocampus |
topic |
temporal lobe epilepsy child adolescent sclerosis hippocampus |
description |
INTRODUCTION: Mesial temporal sclerosis is not a frequent cause of refractory epilepsy in children, and the its start age is uncertain. OBJECTIVE: To understand the clinic feature of children with mesial temporal sclerosis diagnosis. MATERIAL AND METHODS: It was done a literature review about this pathology in children, and it has been found a group of 4 articles that allow a general view about mesial temporal sclerosis in children and other group of 7 articles (case reports or small series) in which mesial temporal sclerosis was diagnosed until five years old. RESULTS: It was evaluated in the first group, febrile seizure that was the most frequent antecedent followed by a status epilepticus and the semiology of the seizures was characterized by oroalimentary automatism, gestural automatism, stunted movement and motor phenomenon.The group of children with mesial temporal sclerosis until five years old stood out due to the high incidence of status epilepticus (84,6%), by the number of children with altered neuropsycomotor development (46%), and by lesion in most of bilateral cases (53,8%) , suggesting that the bilateral form of the mesial temporal sclerosis might be a distinct pathology, and not necessarily the progression of a unilateral beginning picture. Another important thing to stand out in this group is the documentation by MR in edema in hippocampus after a status epilepticus and posterior atrophy of this structure. CONCLUSION: mesial temporal sclerosis can to appear still in early life and in any cases can to present an evolutional character and dependent from a previous aggression to the hippocampus. |
publishDate |
2007 |
dc.date.none.fl_str_mv |
2007-09-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-26492007000300005 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-26492007000300005 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S1676-26492007000300005 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Liga Brasileira de Epilepsia (LBE) |
publisher.none.fl_str_mv |
Liga Brasileira de Epilepsia (LBE) |
dc.source.none.fl_str_mv |
Journal of Epilepsy and Clinical Neurophysiology v.13 n.3 2007 reponame:Journal of epilepsy and clinical neurophysiology (Online) instname:Liga Brasileira de Epilepsia (LBE) instacron:LBE |
instname_str |
Liga Brasileira de Epilepsia (LBE) |
instacron_str |
LBE |
institution |
LBE |
reponame_str |
Journal of epilepsy and clinical neurophysiology (Online) |
collection |
Journal of epilepsy and clinical neurophysiology (Online) |
repository.name.fl_str_mv |
Journal of epilepsy and clinical neurophysiology (Online) - Liga Brasileira de Epilepsia (LBE) |
repository.mail.fl_str_mv |
||jecnpoa@terra.com.br |
_version_ |
1754734659153952768 |