摘要
目的 探讨感觉性共济失调型 CIDP的临床特点和发病机理。方法 总结 16例以深感觉障碍为主要表现的 CIDP患者的临床资料。结果 本组患者均主要表现为深感觉障碍性共济失调 ,病程长 ,易缓解复发 ,脑脊液蛋白升高显著 ,病理改变同一般 CIDP,糖皮质激素远期疗效好。结论 感觉性共济失调型 CIDP是 CIDP的一种特殊亚型 ,发病机理可能是免疫反应主要侵及脊髓背根的深感觉纤维。
Objective To explore the clinical characteristics and pathogenic mechanism of sensory ataxia form of GBS. Methods To Summarize clinical data of 16 cases with sensory ataxia form of GBS. Results The main clinical manifestations was sensory ataxia. The disease relieved and recured easily and had long cause. The protein in CSF increased significantly. Pathological feature was same with general CIDP. Treatment of glucocorticoid was satisfied. Conclusion Sensory ataxia form of GBS was one sub type of CIDP. Pathogenic mechanism was perhapse that immunoreaction attacked proproioceptive sense fibre of radix dorsalis.
出处
《中风与神经疾病杂志》
CAS
CSCD
北大核心
2000年第2期111-112,共2页
Journal of Apoplexy and Nervous Diseases
