髓鞘少突胶质细胞糖蛋白
医学
病理
多发性硬化
横贯性脊髓炎
少突胶质细胞
免疫学
视神经脊髓炎
抗体
自身免疫
脊髓炎
脊髓
髓鞘
实验性自身免疫性脑脊髓炎
中枢神经系统
内科学
精神科
作者
Michela Ada Noris Ferilli,Claudia Papi,Mario Sabatelli,Cesare Colosimo,Raffaele Iorio
标识
DOI:10.1016/j.jneuroim.2022.577875
摘要
Abstract
Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS) is an inflammatory syndrome characterized by the predominant involvement of the pons, the cerebellum and the spinal cord with a distinct corticosteroid responsiveness. To date, several cases of neurological disorders with a CLIPPERS-like phenotype have been described, including patients with Immunoglobulin G (IgG) antibodies binding to myelin oligodendrocyte glycoprotein (MOG). We herein report the case of a man with myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) fulfilling the diagnostic criteria for probable CLIPPERS and a literature review of CLIPPERS-mimicking patients with MOG-IgG.
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