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Clin Neurol Neurosurg ; 217: 107247, 2022 06.
Article in English | MEDLINE | ID: mdl-35483186

ABSTRACT

A seven-year-old girl with history of type I diabetes and no history of seizures presented for altered mental status with convulsions nearly one week after a febrile illness. Serum and laboratory studies were normal with EEG showing biparietal fast activity and seizures originating from right occipital lobe consistent with FIRES. A collaborative decision was ultimately made to withdraw care. Post-mortem whole brain histopathological examination revealed diffuse abnormalities in multiple areas including both parietal lobes and the right parieto-occipital junction consistent with focal cortical dysplasia type IIa. We believe this to be the first report that describes focal cortical dysplasia type IIa co-localizing with epileptogenic areas on EEG in a case of FIRES, and recommend that focal cortical dysplasia be considered as an etiology early in the course of FIRES.


Subject(s)
Drug Resistant Epilepsy , Encephalitis , Epileptic Syndromes , Malformations of Cortical Development , Child , Drug Resistant Epilepsy/etiology , Drug Resistant Epilepsy/surgery , Electroencephalography , Encephalitis/complications , Epilepsy , Epileptic Syndromes/complications , Female , Humans , Magnetic Resonance Imaging/adverse effects , Malformations of Cortical Development/complications , Malformations of Cortical Development/diagnostic imaging , Malformations of Cortical Development, Group I , Seizures/etiology , Treatment Outcome
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