Hemimegalencephaly and epilepsy: an overview

Detalhes bibliográficos
Autor(a) principal: Terra-Bustamante,Vera C.
Data de Publicação: 2006
Outros Autores: Machado,Hélio R., Sakamoto,Américo C.
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=S1676-26492006000300010
Resumo: INTRODUCTION: Cerebral cortical development is a highly complex process influenced by environmental, genetic and functional abnormalities. Hemimegalencephaly (HME) is a rare brain malformation that involves overgrowth of one hemisphere. Clinically macrocephaly, mental retardation, contralateral hemiparesis, hemianopsia and intractable epilepsy may be present. Diagnosis is mainly done with image and clinical findings. MRI typically reveals an enlarged cerebrum involving at least one lobe, with a thickened cortex; broad gyres; abnormal gray-white matter differentiation with abnormal sign; neuronal heterotopia, ventricle asymmetry, and basal ganglia and internal capsule abnormalities. Electroencephalographic abnormalities usually involve the affected hemisphere, with an asymmetric amplitude of the normal, age-related rhythms; slow, rhythmic or fast activity and multifocal unilateral or bilateral high-amplitude spikes and spike-wave complexes. Histopathologic changes include abnormal gyrification, with loss of cortical lamination, neuronal heterotopia, gliosis, large bizarre neurons and balloon-cells. The presence of highly refractory seizures in patients with HME is an important factor to consider epilepsy surgery in these patients. METHODS: Multiple surgical techniques are actually being used for hemispheric disconnection. We discuss here the main surgical techniques that are used for hemispheric disconnection. CONCLUSIONS: Postsurgery outcome for HME may be not as good as that for focal lesions with approximately 40% of patients being seizure free, but the main indication for surgery in these patients may be preventing additional cognitive injury and developmental delay. Surgical complications are observed in most of the series of patients with HME submitted to hemispheric surgery. Minimal resections may contribute do diminish surgical complications.
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spelling Hemimegalencephaly and epilepsy: an overviewhemimegalencephlyepilepsysurgeryINTRODUCTION: Cerebral cortical development is a highly complex process influenced by environmental, genetic and functional abnormalities. Hemimegalencephaly (HME) is a rare brain malformation that involves overgrowth of one hemisphere. Clinically macrocephaly, mental retardation, contralateral hemiparesis, hemianopsia and intractable epilepsy may be present. Diagnosis is mainly done with image and clinical findings. MRI typically reveals an enlarged cerebrum involving at least one lobe, with a thickened cortex; broad gyres; abnormal gray-white matter differentiation with abnormal sign; neuronal heterotopia, ventricle asymmetry, and basal ganglia and internal capsule abnormalities. Electroencephalographic abnormalities usually involve the affected hemisphere, with an asymmetric amplitude of the normal, age-related rhythms; slow, rhythmic or fast activity and multifocal unilateral or bilateral high-amplitude spikes and spike-wave complexes. Histopathologic changes include abnormal gyrification, with loss of cortical lamination, neuronal heterotopia, gliosis, large bizarre neurons and balloon-cells. The presence of highly refractory seizures in patients with HME is an important factor to consider epilepsy surgery in these patients. METHODS: Multiple surgical techniques are actually being used for hemispheric disconnection. We discuss here the main surgical techniques that are used for hemispheric disconnection. CONCLUSIONS: Postsurgery outcome for HME may be not as good as that for focal lesions with approximately 40% of patients being seizure free, but the main indication for surgery in these patients may be preventing additional cognitive injury and developmental delay. Surgical complications are observed in most of the series of patients with HME submitted to hemispheric surgery. Minimal resections may contribute do diminish surgical complications.Liga Brasileira de Epilepsia (LBE)2006-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-26492006000300010Journal of Epilepsy and Clinical Neurophysiology v.12 n.2 2006reponame:Journal of epilepsy and clinical neurophysiology (Online)instname:Liga Brasileira de Epilepsia (LBE)instacron:LBE10.1590/S1676-26492006000300010info:eu-repo/semantics/openAccessTerra-Bustamante,Vera C.Machado,Hélio R.Sakamoto,Américo C.eng2007-05-21T00:00:00Zoai:scielo:S1676-26492006000300010Revistahttp://epilepsia.org.br/publicacoes/ONGhttps://old.scielo.br/oai/scielo-oai.php||jecnpoa@terra.com.br1980-53651676-2649opendoar:2007-05-21T00:00Journal of epilepsy and clinical neurophysiology (Online) - Liga Brasileira de Epilepsia (LBE)false
dc.title.none.fl_str_mv Hemimegalencephaly and epilepsy: an overview
title Hemimegalencephaly and epilepsy: an overview
spellingShingle Hemimegalencephaly and epilepsy: an overview
Terra-Bustamante,Vera C.
hemimegalencephly
epilepsy
surgery
title_short Hemimegalencephaly and epilepsy: an overview
title_full Hemimegalencephaly and epilepsy: an overview
title_fullStr Hemimegalencephaly and epilepsy: an overview
title_full_unstemmed Hemimegalencephaly and epilepsy: an overview
title_sort Hemimegalencephaly and epilepsy: an overview
author Terra-Bustamante,Vera C.
author_facet Terra-Bustamante,Vera C.
Machado,Hélio R.
Sakamoto,Américo C.
author_role author
author2 Machado,Hélio R.
Sakamoto,Américo C.
author2_role author
author
dc.contributor.author.fl_str_mv Terra-Bustamante,Vera C.
Machado,Hélio R.
Sakamoto,Américo C.
dc.subject.por.fl_str_mv hemimegalencephly
epilepsy
surgery
topic hemimegalencephly
epilepsy
surgery
description INTRODUCTION: Cerebral cortical development is a highly complex process influenced by environmental, genetic and functional abnormalities. Hemimegalencephaly (HME) is a rare brain malformation that involves overgrowth of one hemisphere. Clinically macrocephaly, mental retardation, contralateral hemiparesis, hemianopsia and intractable epilepsy may be present. Diagnosis is mainly done with image and clinical findings. MRI typically reveals an enlarged cerebrum involving at least one lobe, with a thickened cortex; broad gyres; abnormal gray-white matter differentiation with abnormal sign; neuronal heterotopia, ventricle asymmetry, and basal ganglia and internal capsule abnormalities. Electroencephalographic abnormalities usually involve the affected hemisphere, with an asymmetric amplitude of the normal, age-related rhythms; slow, rhythmic or fast activity and multifocal unilateral or bilateral high-amplitude spikes and spike-wave complexes. Histopathologic changes include abnormal gyrification, with loss of cortical lamination, neuronal heterotopia, gliosis, large bizarre neurons and balloon-cells. The presence of highly refractory seizures in patients with HME is an important factor to consider epilepsy surgery in these patients. METHODS: Multiple surgical techniques are actually being used for hemispheric disconnection. We discuss here the main surgical techniques that are used for hemispheric disconnection. CONCLUSIONS: Postsurgery outcome for HME may be not as good as that for focal lesions with approximately 40% of patients being seizure free, but the main indication for surgery in these patients may be preventing additional cognitive injury and developmental delay. Surgical complications are observed in most of the series of patients with HME submitted to hemispheric surgery. Minimal resections may contribute do diminish surgical complications.
publishDate 2006
dc.date.none.fl_str_mv 2006-06-01
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=S1676-26492006000300010
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-26492006000300010
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S1676-26492006000300010
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.12 n.2 2006
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
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