Brusa Roberta, Faravelli Irene, Gagliardi Delia, Magri Francesca, Cogiamanian Filippo, Saccomanno Domenica, Cinnante Claudia, Mauri Eleonora, Abati Elena, Bresolin Nereo, Corti Stefania, Comi Giacomo Pietro
Neurology Unit, Department of Pathophysiology and Transplantation, Dino Ferrari Center, IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Neurology Unit, Department of Pathophysiology and Transplantation, Dino Ferrari Center, IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.
Front Neurol. 2019 Aug 13;10:823. doi: 10.3389/fneur.2019.00823. eCollection 2019.
Here, we describe a 79-year-old man, admitted to our unit for worsening diplopia and fatigue, started a few weeks after an episode of bronchitis and flu vaccination. Past medical history includes myasthenia gravis (MG), well-controlled by Pyridostigmine, Azathioprine, and Prednisone. During the first days, the patient developed progressive ocular movement abnormalities up to complete external ophthalmoplegia, severe limb and gait ataxia, and mild dysarthria. Deep tendon reflexes were absent in lower limbs. Since not all the symptoms were explainable with the previous diagnosis of myasthenia gravis, other etiologies were investigated. Brain MRI and cerebrospinal fluid analysis were normal. Electromyography showed a pattern of predominantly sensory multiple radiculoneuritis. Suspecting Miller Fisher syndrome (MFS), the patient was treated with plasmapheresis with subsequent clinical improvement. Antibodies against GQ1b turned out to be positive. MFS is an immune-mediated neuropathy presenting with ophthalmoplegia, ataxia, and areflexia. Even if only a few cases of MFS overlapping with MG have been described so far, the coexistence of two different autoimmune disorders can occur. It is always important to evaluate possible differential diagnosis even in case of known compatible diseases, especially when some clinical features seem atypical.
在此,我们描述一名79岁男性,因复视加重和疲劳入住我院,症状在一次支气管炎发作和流感疫苗接种几周后出现。既往病史包括重症肌无力(MG),通过吡啶斯的明、硫唑嘌呤和泼尼松控制良好。在最初几天,患者出现进行性眼球运动异常,直至完全性眼外肌麻痹、严重的肢体和步态共济失调以及轻度构音障碍。下肢深腱反射消失。由于并非所有症状都能用先前诊断的重症肌无力来解释,因此对其他病因进行了调查。脑部MRI和脑脊液分析均正常。肌电图显示主要为感觉性多发性神经根神经炎模式。怀疑为米勒费希尔综合征(MFS),对患者进行了血浆置换治疗,随后临床症状改善。抗GQ1b抗体结果呈阳性。MFS是一种免疫介导的神经病变,表现为眼外肌麻痹、共济失调和反射消失。即使到目前为止仅描述了少数几例MFS与MG重叠的病例,但两种不同自身免疫性疾病共存的情况仍可能发生。即使在已知存在相符疾病的情况下,评估可能的鉴别诊断也始终很重要,尤其是当某些临床特征看起来不典型时。