Chen Nan, Cai Hanyu, Cheng Jianhua
Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Front Neurol. 2022 Feb 7;12:814453. doi: 10.3389/fneur.2021.814453. eCollection 2021.
In this case report, we describe a patient who was first diagnosed with Miller Fisher syndrome (MFS) combined with myasthenia gravis (MG). A 58-year-old male patient presented with acute dysarthria with dizziness, ophthalmoplegia, absence of deep tendon reflexes in the extremities, and ataxia. Lumbar puncture 1 week after onset showed albuminocytologic dissociation and serum antibodies against GQ1b and GT1a turned out to be positive. Ultimately, the patient was diagnosed with MFS, which is a rare variant of Guillain-Barre syndrome. Because the clinical manifestations of the patient could not exclude MG, electromyography, and serum muscle weakness antibody profile were performed. The results showed positive for axillary nerve repetitive electrical stimulation and antibodies against acetylcholine receptor (AChR) and titin were detected, so the patient was diagnosed with MG at the same time. Even though only five cases of overlapping MFS and MG so far have been described, two different autoimmune diseases may coexist. When one disease presents with uncommon symptoms, careful identification of the presence or absence of other comorbid diseases should be required.
在本病例报告中,我们描述了一名最初被诊断为米勒费雪综合征(MFS)合并重症肌无力(MG)的患者。一名58岁男性患者出现急性构音障碍,伴有头晕、眼肌麻痹、四肢腱反射消失和共济失调。发病1周后腰椎穿刺显示蛋白细胞分离,血清抗GQ1b和GT1a抗体呈阳性。最终,该患者被诊断为MFS,这是格林-巴利综合征的一种罕见变异型。由于患者的临床表现不能排除MG,因此进行了肌电图检查和血清肌无力抗体谱检测。结果显示腋神经重复电刺激阳性,检测到抗乙酰胆碱受体(AChR)和抗肌联蛋白抗体,因此该患者同时被诊断为MG。尽管迄今为止仅描述了5例MFS和MG重叠的病例,但两种不同的自身免疫性疾病可能同时存在。当一种疾病出现不常见症状时,应仔细鉴别是否存在其他合并疾病。