| Literature DB >> 29141829 |
Lei Zhou1, Jingzi ZhangBao1, Haiqing Li2, Xiaoyang Li1, Yongheng Huang3, Min Wang3, Chongbo Zhao4, Jiahong Lu1, Chuanzhen Lu1, Yuxin Li5, Chao Quan6.
Abstract
We report the case of a patient who initially presented with fever, headache and seizure. MRI revealed a fluid attenuation inversion recovery (FLAIR) high-intensity lesion involving the right temporal, parietal and occipital cortex. Afterwards, the patient developed three recurrent episodes, manifested as brainstem encephalitis, optic neuritis and ADEM-like illness successively, indicating demyelination. Both of his serum anti-MOG and CSF anti-NMDAR antibodies were proved positive by transfected cell based assays. We consider our case to have cortical encephalitis due to certain autoimmune mechanism initially, and then developed MOG-antibody mediated recurrent demyelination in the following episodes.Entities:
Keywords: Autoimmune encephalitis (AIE); Myelin oligodendrocyte glycoprotein (MOG); N-methyl-D-aspartate receptor (NMDAR)
Mesh:
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Year: 2017 PMID: 29141829 DOI: 10.1016/j.msard.2017.09.023
Source DB: PubMed Journal: Mult Scler Relat Disord ISSN: 2211-0348 Impact factor: 4.339