论文部分内容阅读
Fisher综合征也称Millre-Fishre Syndroms,是急性炎症性脱髓鞘性多发性神经病(AIDP)即吉兰-巴雷综合征(GBS)的变异型,约占GBS的5%[1],主要表现有三大特点:眼外肌麻痹、共济失调、腱反射减退或消失,伴脑脊液蛋白-细胞分离,大部分患者在病前1～3周有呼吸道或胃肠道感染。该病临床较少见,易被误诊。本文对一例Fisher综合征误诊病例进行分析,报道如下。1病历资料患者男,73岁,因头晕、视物成双28d,双眼睑下垂8d入院。患者于入院28d前起无明显诱因下出现头晕、视物成
Fisher’s syndrome, also known as Millre-Fishre Syndroms, is a variant of acute inflammatory demyelinating polyneuropathy (AIDP), known as GBS, accounting for about 5% of GBS [1], mainly There are three major characteristics: extraocular muscle paralysis, ataxia, tendon reflex or disappear, with cerebrospinal fluid protein - cell separation, most patients 1 to 3 weeks before illness with respiratory or gastrointestinal infections. The disease is less common, easily misdiagnosed. This article analyzes a case of misdiagnosis of Fisher syndrome, reported as follows. A patient information Male, 73 years old, due to dizziness, depending on the material into a double 28d, double eyelid ptosis 8d admission. Patients 28d before admission no obvious incentive to appear dizzy, depending on the material into