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儿童先天性肝纤维化

Congenital hepatic fibrosis in children.

作者信息

Alvarez F, Bernard O, Brunelle F, Hadchouel M, Leblanc A, Odièvre M, Alagille D

出版信息

J Pediatr. 1981 Sep;99(3):370-5. doi: 10.1016/s0022-3476(81)80320-4.

Abstract

Twenty-seven children with congenital hepatic fibrosis were followed for three months to 12 years. Hepatosplenomegaly, normal liver function tests, and kidney abnormalities were present in most patients, indicating that a correct diagnosis of congenital hepatic fibrosis could be made using simple clinical, biologic, and radiologic criteria. Esophageal endoscopy showed varices in 21 patients. Sixteen children underwent portal-systemic shunt surgery. Follow-up examinations did not show any impairment of liver function or any sign of hepatic encephalopathy. Cholangitis was present in only three children.

摘要

对27例先天性肝纤维化患儿进行了3个月至12年的随访。大多数患者存在肝脾肿大、肝功能检查正常以及肾脏异常,这表明使用简单的临床、生物学和放射学标准即可对先天性肝纤维化做出正确诊断。食管内镜检查显示21例患者有静脉曲张。16名儿童接受了门体分流手术。随访检查未显示肝功能有任何损害或肝性脑病的任何迹象。仅3名儿童发生胆管炎。

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