摘要
目的分析Miller-Fisher综合症的临床特点,以提高诊断识别率.方法回顾性分析32例Miller-Fisher综合症的临床资料.结果 32例患者中29例发病前有前驱症状,19例患者表现典型的三联征,所有患者均存在蛋白-细胞分离现象,28例患者存在免疫球蛋白的增高,免疫球蛋白治疗患者的预后良好.结论 Miller-Fisher综合症为感染后自身免疫性疾病,多有前驱症状,有多样性临床表现,静注免疫球蛋白对基治疗效果好.
Objective To Analysis the clinical significance of Miller-Fisher syndrome to intend to find a way to increase the identification rate of diagnosis.Methods The clinical materials from 32 patients with Miller-Fisher syndrome was reported by means of retrospective analysis.Results Among the 32 cases,there are preliminary symptoms in 29 cases,typical triad in 19 cases,and the phenomenon of protein-cell separation in all cases.Moreover,immunity-globin increases in 28 cases,and is very effective in the treatment of the patients.Conclusions Miller-Fisher syndrome belongs to immunity diseases resulting from sepsis.It indicates multiple clinical syndrome and can be treated effectively by vein injection of immune globin
出处
《昆明医学院学报》
2011年第5期65-67,共3页
Journal of Kunming Medical College