Case report: A patient with meningoencephalitis followed by asymptomatic anti-myelin oligodendrocyte glycoprotein antibodyrelated disorder

被引:0
|
作者
Li, Yunjie [1 ]
Liu, Xia [1 ]
Wang, Jingxuan [1 ]
Pan, Chao [1 ]
Tang, Zhouping [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Wuhan 430030, Hubei, Peoples R China
来源
JOURNAL OF NEURORESTORATOLOGY | 2022年 / 10卷 / 03期
基金
中国国家自然科学基金;
关键词
Myelin oligodendrocyte glycoprotein; Septic meningoencephalitis; MOG antibody; Demyelination; CLINICAL SPECTRUM; MOG; MENINGITIS; ANTIBODIES; DISEASE;
D O I
10.1016/j.jnrt.2022.100007
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We describe a unique case in which a patient was initially diagnosed with meningoencephalitis and then detected anti-myelin oligodendrocyte glycoprotein (MOG) antibody and demyelinating brain lesions. A 43-year-old Chinese man who complained of headache and fever, was diagnosed with meningoencephalitis after cerebrospinal fluid (CSF) analysis. One month after onset, brain imaging revealed multiple lesions in bilateral white matter, and the anti-MOG antibody was detected in his serum and CSF (titer is 1:32 and 1:10, respectively). After a 3-month glucocorticoid therapy, repeated brain imaging and serological analysis for anti-MOG antibodies showed significant improvement. Multiple intracranial demyelinating lesions secondary to meningoencephalitis may be accompanied by anti-MOG antibody positivity, which can be reversed by hormone therapy. (c) 2022 The Authors. Published by Elsevier Ltd on behalf of Tsinghua University Press. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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页数:4
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