摘要
目的:分析14例Miller Fisher综合征的临床特点和预后。方法:回顾性分析1998年1月至2007年3月我院收治的14例Miller Fisher综合征患者,应用Microsoft Access 2003建立数据库,分析患者的各种症状、体征和各项检查和预后。结果:病前感染者11例,其中肠道感染8例,双侧动眼神经损害14例,眼内肌的损害7例,对光反射消失5例,共济失调9例,头晕7例,腱反射减低12例,肌力减退7例,周围神经损害5例,病理征3例,蛋白-细胞分离12例,影像学异常2例,肌电图改变7例。结论:Miller Fisher综合征临床症状复杂,可在经典的三联征基础上伴有其他体征,也可仅有其中的两联征,预后较好。
Objective： To analysis the clinical features and prognosis of patients with Miller Fisher syndrome. Method： The inpatients with Miller Fisher syndrome from January 1998 to March 2007 were retrospectively reviewed. A database was made with Microsoft Access 2003, include clinical symptoms, signs, all kind of examination, and prognosis. Results： Of all the cases, 11 patients were precede by infection, 14 patients had diplopia, 9 patients had ataxia, 7 patients had dizziness, 12 patients had areflexia, 7 patients had internal ophthalmoplegia, 5 patients had disappeared light reflex, 7 patients had reduced muscle force, 5 patients had peripheral lesion, 3 patients had Babinski sign, 12 patients had protein-cell separation, 2 patients had abnormal image, 7 patients had abnormal electromyography. Conclusion： Miller Fisher syndrome had a complex clinical features, often occurred in addition to the characteristic triad or only occurred two symptoms. The prognosis of Miller Fisher syndrome is well.
出处
《脑与神经疾病杂志》
2007年第3期210-212,共3页
Journal of Brain and Nervous Diseases
