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An Overlapping Case of Miller Fisher Syndrome and the Pharyngeal-Cervical-Brachial Variant of Guillain-Barré Syndrome

机译:Miller Fisher综合征和Guillain-Barré综合征的咽颈-臂肱变异的重叠病例

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A 55 years-old Caucasian male presented initially in the emergency room reporting myalgia, chills and fever. Physical exam and laboratory tests were unremarkable and he was discharged with symptomatic care. He returned to our ER two weeks later reporting dizziness, loss of balance, blurred vision, mild dysarthria and bilateral hand paresthesia. On examination he presented complete bilateral ophthalmoplegia, mild dysarthria, left finger-to-nose dysmetria, ataxia, areflexia and bilateral hand hypoesthesia without fever. Blood tests and head computed tomography were normal. The patient was admitted to the Internal Medicine department. On second day inwards the patient presented dysphagia. Head magnetic resonance angiogram showed no signs of ischemia or vascular disease and a lumbar puncture was performed but no pleocytosis, albumin-cytological dissociation or hypoglycorrhachia was present. Despite the normal results we suspected of a Guillain–Barré syndrome variant, and started treatment with intravenous immunoglobulin (IVIG) in a dose of 400mg per kilogram and continued for five days with immediate neurological improvement. We present a rare?overlapping?case of?Miller Fisher?syndrome and Pharyngeal-Cervical-Brachial variant of Guillain–Barré syndrome.
机译:一名55岁的白人男性最初出现在急诊室,报告有肌痛,发冷和发烧。体格检查和实验室检查无异常,对症出院。两周后他返回急诊室,报告头晕,失去平衡,视力模糊,轻度构音障碍和双侧手感觉异常。在检查中,他表现出完全的双侧眼肌麻痹,轻度构音障碍,左手指到鼻子的异位症,共济失调,反射力减退和双侧手感觉不足而没有发烧。验血和头部CT检查正常。该患者入院内科。在第二天,患者出现吞咽困难。头部磁共振血管造影未显示出缺血或血管疾病的迹象,并且进行了腰穿,但未出现胸膜增多症,白蛋白细胞学解离或低血糖症。尽管结果正常,我们仍怀疑是格林-巴利综合征的一种变异,并开始以每公斤400mg的剂量使用静脉注射免疫球蛋白(IVIG)进行治疗,并持续5天,神经系统立即得到改善。我们提出了米勒·费雪综合症和格林-巴雷综合症的咽-颈-臂肱变体的一种罕见的“重叠”病例。

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