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[先天性胆管疾病]

[Congenital disorders of the biliary ducts].

作者信息

Gauthier F, Hadchouel M

机构信息

Département de pédiatrie et INSERM U347 Hôpital de Bicêtre 94275 Le Kremlin-Bicêtre.

出版信息

Rev Prat. 2000 Dec 1;50(19):2142-5.

Abstract

Congenital disorders of the bile ducts manifesting as neonatal cholestasis, are: biliary atresia, Alagille syndrome and neonatal sclerosing cholangitis. Biliary atresia must be considered as a neonatal surgical emergency: diagnosis and therapeutic intervention should be completed before one month of age. Survival at 10 years is about 70%, 14% without and 56% with liver transplantation. The cause of the disease is unknown. Alagille syndrome is defined by the association of bile duct paucity, pulmonary stenosis, butterfly-like vertebrae, peculiar facies and posterior embryotoxon. JAGGEDI gene mutations have been identified allowing prenatal diagnosis. The diagnosis of neonatal sclerosing cholangitis can only be performed by cholangiography.

摘要

表现为新生儿胆汁淤积的先天性胆管疾病有

胆道闭锁、阿拉吉耶综合征和新生儿硬化性胆管炎。胆道闭锁必须被视为新生儿外科急症:诊断和治疗干预应在1月龄前完成。10年生存率约为70%,未进行肝移植的为14%,进行肝移植的为56%。该病病因不明。阿拉吉耶综合征的定义是胆管稀少、肺动脉狭窄、蝶形椎骨、特殊面容和后胚胎环的联合表现。已鉴定出JAGGEDI基因突变,可进行产前诊断。新生儿硬化性胆管炎只能通过胆管造影进行诊断。

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