Rashid Muhammad Humayoun, Yasir Hafiz Khawaja Muhammad, Zahid Muhammad Farhan, Khan Ahmad Ali, Ahmad Mehjabeen
Neurology, Bakhtawar Amin Medical and Dental College, Multan, PAK.
Internal Medicine, Nishtar Medical University and Hospital, Multan, PAK.
Cureus. 2020 Mar 9;12(3):e7223. doi: 10.7759/cureus.7223.
Miller Fisher syndrome (MFS) is a rare variant of Guillain-Barre syndrome (GBS) which usually presents with descending paralysis. Common symptoms are ophthalmoplegia, ataxia, and areflexia. Our case presented with an atypical presentation. A 52-year old lady presented to the neurology outpatient department with frequent falls, blurring and doubling of vision and difficulty swallowing. These symptoms followed mild non-bloody diarrhea for two weeks ago. She had bilateral ptosis, lateral gaze palsy in both eyes, absent gag and cough reflex; she was unable to walk in a straight line and had right-hand grip weakness. Other motor and sensory examination were normal. She was admitted, kept under observation and investigated accordingly. Cerebrospinal fluid (CSF) analysis showed albuminocytologic dissociation. Nerve conduction studies showed slowed conduction in abducent, glossopharyngeal, vagus, and the right ulnar nerve. Blood analysis showed antiganglioside GQ1b antibodies; hence, the diagnosis of MFS, a variant of GBS, was made. Empirically plasmapheresis and then after confirmation intravenous immunoglobulins (IVIG) were used as treatment options. She recovered gradually within four weeks.
米勒-费雪综合征(MFS)是吉兰-巴雷综合征(GBS)的一种罕见变异型,通常表现为下行性麻痹。常见症状为眼肌麻痹、共济失调和无反射。我们的病例表现不典型。一位52岁女性因频繁跌倒、视力模糊和复视以及吞咽困难就诊于神经内科门诊。这些症状出现在两周前的轻度非血性腹泻之后。她有双侧上睑下垂、双眼外展凝视麻痹、咽反射和咳嗽反射消失;她无法直线行走,右手握力减弱。其他运动和感觉检查正常。她入院后接受观察并进行相应检查。脑脊液(CSF)分析显示蛋白细胞分离。神经传导研究显示展神经、舌咽神经、迷走神经和右侧尺神经传导减慢。血液分析显示抗神经节苷脂GQ1b抗体;因此,诊断为MFS,即GBS的一种变异型。经验性地采用血浆置换,确诊后使用静脉注射免疫球蛋白(IVIG)作为治疗方案。她在四周内逐渐康复。