抗体
视神经
髓鞘
少突胶质细胞
髓鞘碱性蛋白
中枢神经系统
免疫学
白质
视神经脊髓炎
作者
Corey J. Miller,Jeffrey Bennett,Michael S. Lee
标识
DOI:10.1016/j.msard.2020.102455
摘要
We present a case with an atypical presentation of myelin oligodendrocyte glycoprotein associated disease (MOGAD) presenting with optic neuritis, short-segment transverse myelitis, and significant lymphocytic pleocytosis. The degree of lymphocytic pleocytosis in this case was unusually high and prompted extensive workup. Broad infectious and neoplastic work-up was unremarkable and raised the concern for aseptic meningitis. A literature review was performed of similar cases with documented CSF labs (see Table 1), which demonstrates the unique and significant pleocytosis noted in this case.
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