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

IF 3.1 4区 医学 Q2 CLINICAL NEUROLOGY
Yunjie Li, Xia Liu, Jingxuan Wang, Chao Pan, Zhouping Tang
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引用次数: 0

Abstract

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.

病例报告:一例脑膜脑炎合并无症状的抗髓鞘少突胶质细胞糖蛋白抗体相关疾病
我们描述了一个独特的情况下,患者最初被诊断为脑膜脑炎,然后检测抗髓鞘少突胶质细胞糖蛋白(MOG)抗体和脱髓鞘脑病变。一名43岁的中国男性主诉头痛和发烧,经脑脊液(CSF)分析后诊断为脑膜脑炎。发病1个月后,脑显像显示双侧白质多发病变,血清和脑脊液检测到抗mog抗体(滴度分别为1:32和1:10)。糖皮质激素治疗3个月后,反复脑成像和抗mog抗体血清学分析显示有明显改善。脑膜脑炎继发的颅内多发脱髓鞘病变可伴有抗mog抗体阳性,可通过激素治疗逆转。
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来源期刊
Journal of Neurorestoratology
Journal of Neurorestoratology CLINICAL NEUROLOGY-
CiteScore
2.10
自引率
18.20%
发文量
22
审稿时长
12 weeks
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