| Literature DB >> 31342158 |
Kimitoshi Kimura1,2,3, Yoichiro Okada1,4, Chihiro Fujii5, Kenichi Komatsu2, Ryosuke Takahashi1, Sadayuki Matsumoto2, Takayuki Kondo6,7.
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.Entities:
Keywords: Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis; Morvan syndrome; Multiple sclerosis (MS); Myasthenia gravis (MG); Neuromyelitis optica spectrum disorder (NMOSD)
Mesh:
Year: 2019 PMID: 31342158 DOI: 10.1007/s00415-019-09461-3
Source DB: PubMed Journal: J Neurol ISSN: 0340-5354 Impact factor: 4.849