摘要
分析211例格林巴利综合征患者,男多于女(2.1/1),10~30岁多发。约63%有前驱症状,主要表现在呼吸道和胃肠道。多以迅速加重的肌无力为主诉(95.3%),体征有深反射消失或减退(90%),感觉症状较轻(42.6%)。脑脊液有蛋白-细胞分离(83.8%)。IgG24小时合成率与病情及病程相关。电生理表现脱髓鞘特征(93.5%),病理上表现为节段性脱髓鞘和单核细胞浸润(100%)。
In a survey of 211 cases with GBS, males were dorminant than females (2. 1/1) and the peak age were 10 to 30. Approximately 63% had an antecedent events, mainly respiratory and gastrointestinal infections. Motor weakness usually developed repidly and was chief complaint (95. 3% ). Deep tendon reflexes were reduced even absent (90%), but sensory symptoms were mild (42. 6%). The CSF showed albumino cytologic dissociation with increased protein (83. 8% ) and no or very few cells. The CSF twenty four hour synthesis rate of IgG correlates well with course and severity of disease. The electrophysiological feature was demyelination (93. 5% ), pathological features of sural nerve biopsy were segmental demyelination and mononuclear cell infiltration (100% ).
出处
《中国神经免疫学和神经病学杂志》
CAS
1997年第3期164-167,共4页
Chinese Journal of Neuroimmunology and Neurology
关键词
G-B综合征
脱髓鞘
病例报告
Guillain-Barre syndrome
demyelination
twenty-four synthesis-rate of IgG