Gauthier F, Hadchouel M
Département de pédiatrie et INSERM U347 Hôpital de Bicêtre 94275 Le Kremlin-Bicêtre.
Rev Prat. 2000 Dec 1;50(19):2142-5.
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.
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。