视神经炎
医学
髓鞘少突胶质细胞糖蛋白
多发性硬化
多发性神经病
免疫学
脱髓鞘病
髓鞘
抗体
少突胶质细胞
病理
中枢神经系统
内科学
实验性自身免疫性脑脊髓炎
作者
Francesca Bosello,Damiano Marastoni,Francesca Benedetta Pizzini,Chiara Zaffalon,Andrea Zuliani,Giulia Turri,Sara Mariotto,Erika Bonacci,Emilio Pedrotti,Massimiliano Calabrese
标识
DOI:10.1016/j.jneuroim.2022.578011
摘要
Post-infectious immune-mediated neurological complications of Sars-Cov-2 have been increasingly recognized since the novel pandemic emerged. We describe the case of a 74 years-old patient who developed a Myelin Oligodendrocyte Glycoprotein (MOG) antibody-associated unilateral retrobulbar optic neuritis a few weeks after paucisymptomatic COVID-19 disease and, subsequently, after the resolution of the optic neuritis, an acute inflammatory demyelinating polyneuropathy. So far, no cases of these two neurological manifestations have been reported in the same patient. We herein report a case characterized by both manifestations and review the accumulating literature regarding MOG antibody-associated disease following SarsCov-2 infection.
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