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抗髓鞘少突胶质细胞糖蛋白抗体阳性相关的急性播散性脑脊髓炎(ADEM):感染的后遗症。

Seropositive anti-MOG antibody-associated acute disseminated encephalomyelitis (ADEM): a sequelae of infection.

机构信息

Department of Medicine, Touro University California College of Osteopathic Medicine, Vallejo, California, USA

Department of Medicine, Touro University California College of Osteopathic Medicine, Vallejo, California, USA.

出版信息

BMJ Case Rep. 2020 May 19;13(5):e234565. doi: 10.1136/bcr-2020-234565.

Abstract

Acute disseminated encephalomyelitis (ADEM) is a demyelinating, autoimmune disease of the central nervous system (CNS). It causes motor and sensory deficits, altered mental status and other neurological symptoms. Though rarely fatal, it has been associated with residual motor and neurocognitive deficits. Our case consisted of a 4-year-old girl who presented with fatigue and unsteady gait after a respiratory illness. During her hospital course, she became progressively weaker and experienced seizures. Imaging showed sections of demyelination in the CNS, and appropriate treatment was started. Additional labs resulted in positive serum serology. Antimyelin oligodendrocyte glycoprotein (anti-MOG) antibodies were also found, which is a risk factor for relapsing, multiphasic ADEM. To our knowledge, this is the first case of anti-MOG antibody-associated ADEM due to infection. Our patient has made a complete recovery. The parents only report slightly increased fatigue and irritability.

摘要

急性播散性脑脊髓炎(ADEM)是一种中枢神经系统(CNS)脱髓鞘自身免疫性疾病。它可导致运动和感觉功能障碍、精神状态改变和其他神经症状。虽然很少致命,但它与残留的运动和神经认知缺陷有关。我们的病例是一名 4 岁女孩,在呼吸道疾病后出现疲劳和步态不稳。在住院期间,她的病情逐渐恶化,并出现癫痫发作。影像学显示 CNS 有脱髓鞘病变,随后开始了适当的治疗。进一步的实验室检查结果显示血清学呈阳性。还发现了抗髓鞘少突胶质细胞糖蛋白(anti-MOG)抗体,这是复发性、多相 ADEM 的危险因素。据我们所知,这是首例因感染引起的抗 MOG 抗体相关 ADEM 病例。我们的患者已完全康复。家长仅报告轻微的疲劳和烦躁增加。

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