Zhou Zhijian, Chen Xia, Liu Gonglu, Pu Jiali, Wu Jimin
Department of Neurology, Affiliated Shaoxing Hospital of Traditional Chinese Medicine, Zhejiang Chinese Medical University, Shaoxing, China.
Department of Neurology, Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Front Neurol. 2019 Jul 16;10:770. doi: 10.3389/fneur.2019.00770. eCollection 2019.
Inflammatory myositis (IM) and myasthenia gravis (MG) are both immune disorders involving muscle. The concurrent presence of both conditions in the same patient is extremely rare and the diagnosis is important and challenging. Here, we report a case of concurrent myositis and myocarditis and MG without thymoma in a 69-year-old man with progressive proximal muscle weakness and dysphagia. As an atypical finding, the laboratory immunity assay showed the presence of multiple antibodies (acetylcholine receptor-Ab, titin-Ab, M7-Ab, smooth muscle alpha (SMA)-Ab, and citrate acid extract (CAE)-Ab). We predicted that thymoma-associated antibodies (titin-Ab, SMA-Ab, and CAE-Ab) and anti-M7 antibodies play an important role in the concurrent presence of MG and myositis and myocarditis. In this overlap case, immunotherapy was determined to be effective.
炎性肌病(IM)和重症肌无力(MG)均为累及肌肉的免疫性疾病。同一患者同时出现这两种疾病极为罕见,诊断既重要又具有挑战性。在此,我们报告一例69岁男性患者,同时患有肌炎、心肌炎和无胸腺瘤的MG,伴有进行性近端肌无力和吞咽困难。作为一项非典型发现,实验室免疫分析显示存在多种抗体(乙酰胆碱受体抗体、肌联蛋白抗体、M7抗体、平滑肌α(SMA)抗体和柠檬酸提取物(CAE)抗体)。我们推测胸腺瘤相关抗体(肌联蛋白抗体、SMA抗体和CAE抗体)以及抗M7抗体在MG与肌炎和心肌炎的同时存在中起重要作用。在这例重叠病例中,免疫治疗被确定为有效。