Biliary atresia: A condition requiring urgent diagnosis and treatment

被引:3
|
作者
Chardot, C. [1 ]
Debray, D. [1 ]
机构
[1] Hop Necker Enfants Malad, Grp Medicochirurg Hepatol Pediat, F-75015 Paris, France
来源
ARCHIVES DE PEDIATRIE | 2011年 / 18卷 / 04期
关键词
LIVER-TRANSPLANTATION; KASAI OPERATION; PROGNOSIS; FRANCE;
D O I
10.1016/j.arcped.2011.01.015
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Every neonatal jaundice lasting more than 2 weeks needs urgent investigations, beginning with examination of stools colour, and blood tests with total and conjugated serum bilirubin. If neonatal cholestasis (NC) is confirmed, vitamin K should be immediately injected, and the child should be referred to a specialised centre for investigations and treatment. Biliary atresia (BA) is the first cause of NC. Its diagnosis is urgent, since the chance of success of the conservative surgical treatment (Kasai operation or variants) decreases rapidly as the age at surgery increases. Normal ultrasound scans cannot rule out BA. After prompt work-up looking for the main other causes of NC, BA can often be strongly suspected before surgery, and is confirmed by operative findings and cholangiogram if needed. In case of failure to restore the biliary drainage, biliary cirrhosis progresses and leads to liver transplantation, generally in the first years of life. Currently, more than 90% of children with BA can live, with a close to normal quality of life for most of them. Early diagnosis and treatment of BA contribute to decrease the needs for liver transplantation in infancy and childhood. (C) 2011 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:476 / 481
页数:6
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