Mei Zhujun, Wang Jingguo, Wang Junling, Liu Xiaoni, Deng Bo, Yang Wenbo, Zhang Xiang, Chen Xiangjun, Yu Hai
Department of Neurology, Huashan Hospital, Fudan University and Institute of Neurology, Fudan University, Shanghai, China.
Department of Neurology, National Center for Neurological Disorders, Shanghai, China.
Front Immunol. 2025 Jan 14;15:1461024. doi: 10.3389/fimmu.2024.1461024. eCollection 2024.
We report a case of optic neuritis (ON) secondary to autoimmune encephalitis (AE) in a patient with concomitant antibodies to N-methyl-D-aspartate receptor (NMDAR), gamma-aminobutyric acid-B receptor (GABAR), and myelin oligodendrocyte glycoprotein (MOG). The patient exhibited a constellation of symptoms, including vision loss, seizures, mental and behavioral disorders, cognitive impairment, and speech abnormalities. At the two-year follow-up, the patient's symptoms had abated entirely. Overlap syndrome of triple autoimmune antibodies is rare and the coexistence of antibodies to NMDAR, GABAR and MOG has not been reported till now. This case report provides novel experience of diagnosis and treatment in autoimmune overlap syndromes.
我们报告了一例继发于自身免疫性脑炎(AE)的视神经炎(ON)病例,该患者同时存在针对N-甲基-D-天冬氨酸受体(NMDAR)、γ-氨基丁酸B受体(GABAR)和髓鞘少突胶质细胞糖蛋白(MOG)的抗体。患者表现出一系列症状,包括视力丧失、癫痫发作、精神和行为障碍、认知障碍及言语异常。在两年的随访中,患者症状已完全缓解。三重自身免疫抗体重叠综合征罕见,且NMDAR、GABAR和MOG抗体并存至今尚未见报道。本病例报告为自身免疫重叠综合征的诊断和治疗提供了新经验。