Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/26949
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dc.contributor.authorLeong E.C.S.en
dc.contributor.authorSeneviratne U.en
dc.date.accessioned2021-05-14T09:00:20Zen
dc.date.available2021-05-14T09:00:20Zen
dc.date.copyright2020en
dc.date.created20210318en
dc.date.issued2021-03-18en
dc.identifier.citationEpilepsy and Behavior Reports. 14 (no pagination), 2020. Article Number: 100407. Date of Publication: January 2020.en
dc.identifier.issn2589-9864 (electronic)en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/26949en
dc.description.abstractMesial temporal lobe epilepsy, a well-characterized epilepsy syndrome, is most commonly accompanied by the pathological feature of hippocampal sclerosis. Patients with mesial temporal lobe epilepsy with hippocampal sclerosis (MTLE-HS) typically present in childhood to early adolescence. We describe a cohort of patients who presented with their first epileptic seizure in late adulthood with atypical features. We characterized five patients with late-onset MTLE-HS by describing their demographics, electroclinical features, imaging, autoantibody status, and response to antiseizure medication (ASM) therapy. All five patients had their first seizure after the age of 50 with no history of initial precipitating incidents. None of our patients had positive serum or CSF autoantibodies and they have all remained seizure-free for a minimum of two years on ASMs alone. Two patients had motor vehicle crashes associated with seizures whilst three patients experienced seizures in sleep. A milder form of MTLE, previously described as benign TLE, does exist in routine clinical practice. These patients respond well to ASM therapy, but potentially harmful consequences such as motor vehicle crashes can occur in the untreated.Copyright © 2020 The Authorsen
dc.languageEnglishen
dc.languageenen
dc.publisherElsevier Inc.en
dc.relation.ispartofEpilepsy and Behavior Reports-
dc.title"Benign" temporal lobe epilepsy with hippocampal sclerosis: A forgotten entity?.en
dc.typeArticleen
dc.type.studyortrialObservational study (cohort, case-control, cross sectional or survey)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1016/j.ebr.2020.100407en
dc.publisher.placeUnited Statesen
dc.identifier.source2010224821en
dc.identifier.institution(Leong) Monash School of Medicine, Monash University, Victoria, Australia (Seneviratne) Department of Neuroscience, Monash Medical Centre, Clayton, Victoria, Australia (Seneviratne) School of Clinical Sciences at Monash Health, Department of Medicine, Monash University, Melbourne, Victoria, Australia (Seneviratne) Department of Medicine, St. Vincent's Hospital, University of Melbourne, Melbourne, Australiaen
dc.description.addressE.C.S. Leong, Monash University, Wellington Road, Clayton, Melbourne, VIC 3800, Australia. E-mail: emmanuel.msia@gmail.comen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2021 Elsevier B.V., All rights reserved.en
dc.subect.keywordsBenign Hippocampal sclerosis Late-onset Temporal lobe epilepsyen
dc.identifier.authoremailLeong E.C.S.; emmanuel.msia@gmail.comen
dc.identifier.affiliationext(Leong) Monash School of Medicine, Monash University, Victoria, Australia-
dc.identifier.affiliationext(Seneviratne) School of Clinical Sciences at Monash Health, Department of Medicine, Monash University, Melbourne, Victoria, Australia-
dc.identifier.affiliationext(Seneviratne) Department of Medicine, St. Vincent's Hospital, University of Melbourne, Melbourne, Australia-
dc.identifier.affiliationmh(Seneviratne) Department of Neuroscience, Monash Medical Centre, Clayton, Victoria, Australia-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeArticle-
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