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与重症肌无力相关的中枢神经系统自身免疫性疾病的临床特征。

Clinical characteristics of autoimmune disorders in the central nervous system associated with myasthenia gravis.

机构信息

Department of Neurology, Kyoto University Graduate School of Medicine, 54 Kawaharacho, Shogoin, Sakyo-ku, Kyoto, 606-8507, Japan.

Department of Neurology, Kitano Hospital, Tazuke Kofukai Medical Research Institute, 2-4-20 Ogimachi, Kita-ku, Osaka, 530-8480, Japan.

出版信息

J Neurol. 2019 Nov;266(11):2743-2751. doi: 10.1007/s00415-019-09461-3. Epub 2019 Jul 24.

DOI:10.1007/s00415-019-09461-3
PMID:31342158
Abstract

Myasthenia gravis (MG) is occasionally associated with autoimmune diseases in the central nervous system (CNS), such as neuromyelitis optica spectrum disorder (NMOSD), multiple sclerosis (MS), Morvan syndrome, and anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis. Here, we report five original cases associated with autoimmune disorders in the CNS among 42 patients with MG in a single tertiary hospital in Japan (11.9%). In four of these five cases, the second disease developed when the preceding disease was unstable. Accurate diagnosis of the newly developing disease may be difficult in such cases, because some neurological symptoms can be seen in both disorders. This implies the great importance of recognizing the possible co-occurrence of MG and disorders in the CNS. In addition, a comprehensive review of the literature revealed distinct clinical characteristics depending on the associated disease in the CNS, including thymic pathology and temporal relationship between MG and associated CNS disorders. Notably, NMOSD usually develops after the onset of MG and thymectomy, in clear contrast to MS. Thymoma is highly prevalent among patients with Morvan syndrome, in contract to cases with NMOSD and MS. The analysis of clinical characteristics, representing the first such investigation to the best of our knowledge, suggests different pathogeneses of these autoimmune diseases in the CNS, and provides significant implications for clinical practice.

摘要

重症肌无力(MG)偶尔与中枢神经系统(CNS)自身免疫性疾病相关,例如视神经脊髓炎谱系障碍(NMOSD)、多发性硬化症(MS)、莫旺综合征和抗 N-甲基-D-天冬氨酸受体(NMDAR)脑炎。在这里,我们报告了日本一家三级医院的 42 例 MG 患者中 5 例与 CNS 自身免疫性疾病相关的原始病例(11.9%)。在这 5 例中的 4 例中,第二种疾病是在前一种疾病不稳定时发展的。在这种情况下,新发病的准确诊断可能很困难,因为两种疾病都可能出现一些神经系统症状。这意味着认识到 MG 与 CNS 疾病可能同时存在的重要性。此外,对文献的全面回顾揭示了与 CNS 相关疾病相关的不同临床特征,包括胸腺病理学和 MG 与相关 CNS 疾病之间的时间关系。值得注意的是,NMOSD 通常在 MG 和胸腺切除术之后发生,与 MS 形成鲜明对比。莫旺综合征患者的胸腺瘤患病率很高,而 NMOSD 和 MS 则不然。对这些 CNS 自身免疫性疾病的临床特征进行分析,代表了我们迄今为止的首次此类研究,提示这些 CNS 自身免疫性疾病的发病机制不同,并为临床实践提供了重要意义。

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