Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.
Front Immunol. 2021 Apr 23;12:664364. doi: 10.3389/fimmu.2021.664364. eCollection 2021.
The association between multiple sclerosis and anti-N-Methyl-D-Aspartate receptor encephalitis is limited to merely a few case reports, and the exploration of the pathogenic mechanisms underlying the overlap of these two disease entities is very limited. Therefore, case reports and literature review on N-Methyl-D-aspartate receptor antibody in patients with multiple sclerosis are unusual and noteworthy. A young female had the first episode of paresthesia and motor symptoms with positive anti-N-Methyl-D-Aspartate receptor antibody and recovered after immunotherapy, and at the first relapse, the patient developed disorders of consciousness with positive anti-N-Methyl-D-Aspartate receptor antibody, findings of magnetic resonance imaging showed features of autoimmune encephalitis, which was also controlled by immunotherapy. At the second relapse, anti-N-Methyl-D-Aspartate receptor antibody turned negative while oligoclonal bands presented positive, and findings of magnetic resonance imaging showed features of multiple sclerosis. Afterwards, we followed the patient after receiving disease modifying treatment to monitor the efficacy and safety of teriflunomide. Based on literature review, demyelinating diseases patients with anti-neuronal antibody have complex, diverse and atypical symptoms; therefore, high attention and increased alertness are necessary for neurologists. Conclusively, anti-neuronal antibody may present in many neuroinflammatory conditions, and diagnostic criteria should be used with caution if the clinical presentation is atypical, and neurologists should not rely excessively on laboratory tests to diagnose neurological diseases. Timely and comprehensive examination and consideration as well as early standardized treatment are the key factors to reduce patient recurrence and obtain a good prognosis.
多发性硬化症与抗 N-甲基-D-天冬氨酸受体脑炎之间的关联仅限于少数病例报告,并且对这两种疾病实体重叠的发病机制的探索非常有限。因此,在多发性硬化症患者中 N-甲基-D-天冬氨酸受体抗体的病例报告和文献复习是不常见且值得注意的。一名年轻女性首次出现感觉异常和运动症状,抗 N-甲基-D-天冬氨酸受体抗体阳性,经免疫治疗后恢复;首次复发时,患者出现意识障碍,抗 N-甲基-D-天冬氨酸受体抗体阳性,磁共振成像显示自身免疫性脑炎特征,经免疫治疗后也得到控制。第二次复发时,抗 N-甲基-D-天冬氨酸受体抗体转为阴性,寡克隆带阳性,磁共振成像显示多发性硬化症特征。之后,我们对接受疾病修饰治疗的患者进行随访,以监测特立氟胺的疗效和安全性。基于文献复习,抗神经元抗体的脱髓鞘疾病患者症状复杂、多样且不典型;因此,神经科医生需要高度关注和提高警惕。总之,抗神经元抗体可能存在于许多神经炎症性疾病中,如果临床表现不典型,应谨慎使用诊断标准,神经科医生不应过度依赖实验室检查来诊断神经系统疾病。及时、全面的检查和考虑以及早期的标准化治疗是减少患者复发和获得良好预后的关键因素。