| Literature DB >> 26984094 |
Soichiro Numa1, Takashi Kasai, Takayuki Kondo, Yukie Kushimura, Ayaka Kimura, Hisashi Takahashi, Kanako Morita, Akihiro Tanaka, Yu-Ichi Noto, Tomoyuki Ohara, Masanori Nakagawa, Toshiki Mizuno.
Abstract
Acute disseminated encephalomyelitis (ADEM) followed by optic neuritis (ON) has been reported as a distinct phenotype associated with anti-myelin oligodendrocyte protein (MOG) antibody. We herein report the case of a 37-year-old woman who was diagnosed with ADEM at 4 years old of age and who subsequently developed ON followed by recurrent ADEM 33 years after the initial onset. A serum analysis showed anti-MOG antibody positivity. This phenotype has only previously been reported in pediatric cases. Neurologists thus need to be aware that the phenotype may occur in adult patients, in whom it may be assumed to be atypical multiple sclerosis.Entities:
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Year: 2016 PMID: 26984094 DOI: 10.2169/internalmedicine.55.5727
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271