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New-onset Refractory Status Epilepticus Involving the Limbic System, Spinal Cord, and Peripheral Nerves

A healthy 28-year-old woman presented suddenly with intractable status epilepticus: a focal seizure evolved into a generalized seizure preceded by a high fever. Brain magnetic resonance imaging indicated bilateral hyperintensities in the hippocampus on T2-weighted imaging. Electroencephalograms cont...

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Detalles Bibliográficos
Autores principales: Daida, Kensuke, Nishioka, Kenya, Takanashi, Masashi, Kobayashi, Manami, Yoshikawa, Keisuke, Kusunoki, Susumu, Yokoyama, Kazumasa, Hattori, Nobutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7008038/
https://www.ncbi.nlm.nih.gov/pubmed/31511489
http://dx.doi.org/10.2169/internalmedicine.3510-19
Descripción
Sumario:A healthy 28-year-old woman presented suddenly with intractable status epilepticus: a focal seizure evolved into a generalized seizure preceded by a high fever. Brain magnetic resonance imaging indicated bilateral hyperintensities in the hippocampus on T2-weighted imaging. Electroencephalograms continuously demonstrated diffuse sharp waves and poly-spikes. Comprehensive immunomodulation therapies and anti-epileptic drugs did not lead to any improvements. We therefore diagnosed her with cryptogenic limbic encephalitis and new-onset refractory status epilepticus (NORSE). We detected positive anti-ganglioside antibodies, IgG-GQ1b, GD1a, and GT1b, which were negative at six months after the onset. We emphasize the heterogeneous pathogenesis and intractable conditions of NORSE.