Paradoxical ictal EEG lateralization in children with unilateral encephaloclastic lesions

Detalhes bibliográficos
Autor(a) principal: Garzon, Eliana [UNIFESP]
Data de Publicação: 2009
Outros Autores: Gupta, Ajay, Bingaman, William, Sakamoto, Americo C. [UNIFESP], Luders, Hans
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1684/epd.2009.0264
http://repositorio.unifesp.br/handle/11600/31762
Resumo: Background. Describe an ictal EEG pattern of paradoxical lateralization in children with unilateral encephaloclastic hemispheric lesion acquired early in life. Methods. of 68 children who underwent hemispherectomy during 2003-2005, scalp video-EEG and brain MRI of six children with an ictal scalp EEG pattern discordant to the clinical and imaging data were reanalyzed. Medical charts were reviewed for clinical findings and seizure outcome. Results. Age of seizure onset was 1 day-4 years. the destructive MRI lesion was an ischemic stroke in 2, a post-infectious encephalomalacia in 2, and a perinatal trauma and hemiconvulsive-hemiplegic syndrome in one patient each. Ictal EEG pattern was characterized by prominent ictal rhythms with either 3-7 Hz spike and wave complexes or beta frequency sharp waves (paroxysmal fast) over the unaffected (contralesional) hemisphere. Scalp video-EEG was discordant, however, other findings of motor deficits (hemiparesis; five severe, one mild), seizure semiology (4/6), interictal EEG abnormalities (3/6), and unilateral burden of MRI lesion guided the decision for hemispherectomy. After 12-39 months of post-surgery follow up, five of six patients were seizure free and one has brief staring spells. Conclusion. We describe a paradoxical lateralization of the EEG to the good hemisphere in children with unihemispheric encephaloclastic lesions. This EEG pattern is compatible with seizure free outcome after surgery, provided other clinical findings and tests are concordant with origin from the abnormal hemisphere.
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spelling Paradoxical ictal EEG lateralization in children with unilateral encephaloclastic lesionsepilepsy surgeryEEGpediatric epilepsyvideo-EEG in epilepsyBackground. Describe an ictal EEG pattern of paradoxical lateralization in children with unilateral encephaloclastic hemispheric lesion acquired early in life. Methods. of 68 children who underwent hemispherectomy during 2003-2005, scalp video-EEG and brain MRI of six children with an ictal scalp EEG pattern discordant to the clinical and imaging data were reanalyzed. Medical charts were reviewed for clinical findings and seizure outcome. Results. Age of seizure onset was 1 day-4 years. the destructive MRI lesion was an ischemic stroke in 2, a post-infectious encephalomalacia in 2, and a perinatal trauma and hemiconvulsive-hemiplegic syndrome in one patient each. Ictal EEG pattern was characterized by prominent ictal rhythms with either 3-7 Hz spike and wave complexes or beta frequency sharp waves (paroxysmal fast) over the unaffected (contralesional) hemisphere. Scalp video-EEG was discordant, however, other findings of motor deficits (hemiparesis; five severe, one mild), seizure semiology (4/6), interictal EEG abnormalities (3/6), and unilateral burden of MRI lesion guided the decision for hemispherectomy. After 12-39 months of post-surgery follow up, five of six patients were seizure free and one has brief staring spells. Conclusion. We describe a paradoxical lateralization of the EEG to the good hemisphere in children with unihemispheric encephaloclastic lesions. This EEG pattern is compatible with seizure free outcome after surgery, provided other clinical findings and tests are concordant with origin from the abnormal hemisphere.Cleveland Clin Fdn, Neurol Inst, Epilepsy Ctr, Cleveland, OH 44195 USAUniversidade Federal de São Paulo, São Paulo, BrazilUniv Hosp Cleveland, Epilepsy Ctr, Cleveland, OH 44106 USAUniversidade Federal de São Paulo, EPM, São Paulo, BrazilWeb of ScienceJohn Libbey Eurotext LtdCleveland Clin FdnUniversidade Federal de São Paulo (UNIFESP)Univ Hosp ClevelandGarzon, Eliana [UNIFESP]Gupta, AjayBingaman, WilliamSakamoto, Americo C. [UNIFESP]Luders, Hans2016-01-24T13:58:39Z2016-01-24T13:58:39Z2009-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion215-221http://dx.doi.org/10.1684/epd.2009.0264Epileptic Disorders. Montrouge: John Libbey Eurotext Ltd, v. 11, n. 3, p. 215-221, 2009.10.1684/epd.2009.02641294-9361http://repositorio.unifesp.br/handle/11600/31762WOS:000270687600004engEpileptic Disordersinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2022-06-02T09:02:13Zoai:repositorio.unifesp.br/:11600/31762Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652022-06-02T09:02:13Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Paradoxical ictal EEG lateralization in children with unilateral encephaloclastic lesions
title Paradoxical ictal EEG lateralization in children with unilateral encephaloclastic lesions
spellingShingle Paradoxical ictal EEG lateralization in children with unilateral encephaloclastic lesions
Garzon, Eliana [UNIFESP]
epilepsy surgery
EEG
pediatric epilepsy
video-EEG in epilepsy
title_short Paradoxical ictal EEG lateralization in children with unilateral encephaloclastic lesions
title_full Paradoxical ictal EEG lateralization in children with unilateral encephaloclastic lesions
title_fullStr Paradoxical ictal EEG lateralization in children with unilateral encephaloclastic lesions
title_full_unstemmed Paradoxical ictal EEG lateralization in children with unilateral encephaloclastic lesions
title_sort Paradoxical ictal EEG lateralization in children with unilateral encephaloclastic lesions
author Garzon, Eliana [UNIFESP]
author_facet Garzon, Eliana [UNIFESP]
Gupta, Ajay
Bingaman, William
Sakamoto, Americo C. [UNIFESP]
Luders, Hans
author_role author
author2 Gupta, Ajay
Bingaman, William
Sakamoto, Americo C. [UNIFESP]
Luders, Hans
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Cleveland Clin Fdn
Universidade Federal de São Paulo (UNIFESP)
Univ Hosp Cleveland
dc.contributor.author.fl_str_mv Garzon, Eliana [UNIFESP]
Gupta, Ajay
Bingaman, William
Sakamoto, Americo C. [UNIFESP]
Luders, Hans
dc.subject.por.fl_str_mv epilepsy surgery
EEG
pediatric epilepsy
video-EEG in epilepsy
topic epilepsy surgery
EEG
pediatric epilepsy
video-EEG in epilepsy
description Background. Describe an ictal EEG pattern of paradoxical lateralization in children with unilateral encephaloclastic hemispheric lesion acquired early in life. Methods. of 68 children who underwent hemispherectomy during 2003-2005, scalp video-EEG and brain MRI of six children with an ictal scalp EEG pattern discordant to the clinical and imaging data were reanalyzed. Medical charts were reviewed for clinical findings and seizure outcome. Results. Age of seizure onset was 1 day-4 years. the destructive MRI lesion was an ischemic stroke in 2, a post-infectious encephalomalacia in 2, and a perinatal trauma and hemiconvulsive-hemiplegic syndrome in one patient each. Ictal EEG pattern was characterized by prominent ictal rhythms with either 3-7 Hz spike and wave complexes or beta frequency sharp waves (paroxysmal fast) over the unaffected (contralesional) hemisphere. Scalp video-EEG was discordant, however, other findings of motor deficits (hemiparesis; five severe, one mild), seizure semiology (4/6), interictal EEG abnormalities (3/6), and unilateral burden of MRI lesion guided the decision for hemispherectomy. After 12-39 months of post-surgery follow up, five of six patients were seizure free and one has brief staring spells. Conclusion. We describe a paradoxical lateralization of the EEG to the good hemisphere in children with unihemispheric encephaloclastic lesions. This EEG pattern is compatible with seizure free outcome after surgery, provided other clinical findings and tests are concordant with origin from the abnormal hemisphere.
publishDate 2009
dc.date.none.fl_str_mv 2009-09-01
2016-01-24T13:58:39Z
2016-01-24T13:58:39Z
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://dx.doi.org/10.1684/epd.2009.0264
Epileptic Disorders. Montrouge: John Libbey Eurotext Ltd, v. 11, n. 3, p. 215-221, 2009.
10.1684/epd.2009.0264
1294-9361
http://repositorio.unifesp.br/handle/11600/31762
WOS:000270687600004
url http://dx.doi.org/10.1684/epd.2009.0264
http://repositorio.unifesp.br/handle/11600/31762
identifier_str_mv Epileptic Disorders. Montrouge: John Libbey Eurotext Ltd, v. 11, n. 3, p. 215-221, 2009.
10.1684/epd.2009.0264
1294-9361
WOS:000270687600004
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Epileptic Disorders
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 215-221
dc.publisher.none.fl_str_mv John Libbey Eurotext Ltd
publisher.none.fl_str_mv John Libbey Eurotext Ltd
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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