Cited 31 times in
Uncovered primary seizure foci in Lennox-Gastaut syndrome after corpus callosotomy
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 강훈철 | - |
dc.contributor.author | 김동석 | - |
dc.contributor.author | 김흥동 | - |
dc.contributor.author | 이준수 | - |
dc.date.accessioned | 2014-12-20T16:56:21Z | - |
dc.date.available | 2014-12-20T16:56:21Z | - |
dc.date.issued | 2011 | - |
dc.identifier.issn | 0387-7604 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/93664 | - |
dc.description.abstract | PURPOSE: Corpus callosotomy (CC) is a palliative surgical procedure to control atonic, tonic, or generalized tonic-clonic seizure in Lennox-Gastaut syndrome (LGS). Here, we report patients with LGS who underwent resective surgery, following CC better delineating the presumed seizure foci localized in one hemisphere. METHODS: We retrospectively reviewed seven patients with LGS who underwent CC and subsequent cortical resection. The median follow-up duration after lobectomy was 20 months (range, 15-54 months) and three patients had follow-up periods over 24 months. The findings of video electroencephalography (EEG) monitoring, structural and functional neuroimagings were compared between pre- and post-CC. RESULTS: Four patients had Engel class I and one patient had Engel class II outcomes following cortical resection; post-CC, compared to pre-CC, showed better localized ictal/interictal epileptiform discharges in the unilateral frontal area in two patients, in the unilateral parieto-temporo-occipital areas in one patient and in the unilateral fronto-temporal areas in the remaining two patients. Two patients had Engel Class III outcome following cortical resection; post-CC EEG continued to show multifocal epileptiform discharges but predominantly arising from a unilateral frontal area. Following CC, positron emission tomography showed localized glucose hypometabolism of which location was concordant with post-CC EEG abnormalities in all patient. Similarly, ictal/interictal single photon emission computed tomography also showed localized abnormalities concordant with post-CC EEG abnormalities in five of the six patients. Pathological assessment revealed cortical dysplasia in six patients, whereas no pathological abnormality was found in the remaining patient, who obtained Engel Class I outcome following cortical resection. CONCLUSION: CC could change EEG findings, glucose metabolisms and cerebral blood flows, and it is sometimes helpful in delineating the primary seizure focus in patients with LGS. | - |
dc.description.statementOfResponsibility | open | - |
dc.format.extent | 672~677 | - |
dc.relation.isPartOf | BRAIN & DEVELOPMENT | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Child | - |
dc.subject.MESH | Child, Preschool | - |
dc.subject.MESH | Corpus Callosum/surgery* | - |
dc.subject.MESH | Electroencephalography | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Infant | - |
dc.subject.MESH | Intellectual Disability/pathology* | - |
dc.subject.MESH | Intellectual Disability/physiopathology | - |
dc.subject.MESH | Intellectual Disability/surgery* | - |
dc.subject.MESH | Lennox Gastaut Syndrome | - |
dc.subject.MESH | Magnetic Resonance Imaging | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Retrospective Studies | - |
dc.subject.MESH | Seizures/physiopathology | - |
dc.subject.MESH | Seizures/surgery* | - |
dc.subject.MESH | Spasms, Infantile/pathology* | - |
dc.subject.MESH | Spasms, Infantile/physiopathology | - |
dc.subject.MESH | Spasms, Infantile/surgery* | - |
dc.title | Uncovered primary seizure foci in Lennox-Gastaut syndrome after corpus callosotomy | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Pediatrics (소아과학) | - |
dc.contributor.googleauthor | Yun Jung Hur | - |
dc.contributor.googleauthor | Hoon-Chul Kang | - |
dc.contributor.googleauthor | Dong Seok Kim | - |
dc.contributor.googleauthor | Sae Rom Choi | - |
dc.contributor.googleauthor | Heung Dong Kim | - |
dc.contributor.googleauthor | Joon Soo Lee | - |
dc.identifier.doi | 10.1016/j.braindev.2010.11.005 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A00102 | - |
dc.contributor.localId | A00402 | - |
dc.contributor.localId | A01208 | - |
dc.contributor.localId | A03177 | - |
dc.relation.journalcode | J00386 | - |
dc.identifier.eissn | 1872-7131 | - |
dc.identifier.pmid | 21146944 | - |
dc.identifier.url | http://www.sciencedirect.com/science/article/pii/S0387760410002925 | - |
dc.subject.keyword | Lennox–Gastaut syndrome | - |
dc.subject.keyword | Corpus callosotomy | - |
dc.subject.keyword | Primary seizure foci | - |
dc.contributor.alternativeName | Kang, Hoon Chul | - |
dc.contributor.alternativeName | Kim, Dong Seok | - |
dc.contributor.alternativeName | Kim, Heung Dong | - |
dc.contributor.alternativeName | Lee, Joon Soo | - |
dc.contributor.affiliatedAuthor | Kang, Hoon Chul | - |
dc.contributor.affiliatedAuthor | Kim, Dong Seok | - |
dc.contributor.affiliatedAuthor | Kim, Heung Dong | - |
dc.contributor.affiliatedAuthor | Lee, Joon Soo | - |
dc.rights.accessRights | not free | - |
dc.citation.volume | 33 | - |
dc.citation.number | 8 | - |
dc.citation.startPage | 672 | - |
dc.citation.endPage | 677 | - |
dc.identifier.bibliographicCitation | BRAIN & DEVELOPMENT, Vol.33(8) : 672-677, 2011 | - |
dc.identifier.rimsid | 28377 | - |
dc.type.rims | ART | - |
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