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儿童吉兰-巴雷综合征:临床表现、实验室检查结果及类固醇治疗效果

Guillain Barre syndrome in children: clinical manifestations, laboratory findings, and the results of steroid treatment.

作者信息

Ismael S

机构信息

Department of Child Health, Faculty of Medicine, University of Indonesia Jakarta.

出版信息

Paediatr Indones. 1990 Mar-Apr;30(3-4):79-96.

PMID:2075010
Abstract

We report 28 cases diagnosed as GBS in the Department of Child Health, Medical School, University of Indonesia, DR. Cipto Mangunkusumo General Hospital in 7 years period. There were 17 males and 11 females with a ratio of 1.5:1. The age ranged from 9 months to 9.5 years, with a mean age of 4.57 +/- 2.36 years. Twelve (42.86%) cases were preceded by acute respiratory infection, 8 (28.57%) cases by non specific fever, 1 (9.57%) case by gastrointestinal tract infection and 7 (25%) cases did not have any history of acute infection. The clinical manifestations were motor weakness (100%), cranial nerves involvement (14.29%) and disturbance of sensation (17.80%). Most cases (92.86%) showed albuminocytologic dissociation feature with the CSF protein content more than 40 mg/dl. The number of cells was less than 10 cells/mm3 in 96.43% of cases. The specific NCV feature (peripheral NCV decrease) was found in 96.15% of patients and only 1 patient (3.85%) showed normal peripheral NCV. The severity of the disease was in accordance with the prognosis later. Corticosteroid was not beneficial in the treatment of GBS.

摘要

我们报告了印度尼西亚大学医学院儿童健康系、Cipto Mangunkusumo 综合医院在 7 年期间诊断为格林-巴利综合征(GBS)的 28 例病例。其中男性 17 例,女性 11 例,男女比例为 1.5:1。年龄范围为 9 个月至 9.5 岁,平均年龄为 4.57±2.36 岁。12 例(42.86%)在发病前有急性呼吸道感染,8 例(28.57%)有非特异性发热,1 例(9.57%)有胃肠道感染,7 例(25%)无急性感染病史。临床表现为运动无力(100%)、颅神经受累(14.29%)和感觉障碍(17.80%)。大多数病例(92.86%)表现出蛋白细胞分离特征,脑脊液蛋白含量超过 40mg/dl。96.43%的病例细胞数少于 10 个/mm³。96.15%的患者发现有特异性神经传导速度(NCV)特征(周围神经传导速度降低),仅 1 例患者(3.85%)周围神经传导速度正常。疾病的严重程度与后期预后一致。皮质类固醇对格林-巴利综合征的治疗无益。

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