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Biliary atresia
被引:1
|作者:
Zallen, Garret S.
[1
]
Bliss, David W.
Curran, Thomas J.
Harrison, Marvin W.
Silen, Mark L.
机构:
[1] Oregon Hlth Sci Univ, Dept Surg, Div Pediat Surg, Portland, OR 97201 USA
[2] Wright State Univ, Dept Surg, Dayton, OH 45435 USA
关键词:
D O I:
10.1542/pir.27-7-243
中图分类号:
R72 [儿科学];
学科分类号:
100202 ;
摘要:
Extrahepatic biliary atresia is a rare and highly morbid condition. When unrecognized, it progresses inexorably to liver failure and death unless liver transplantation is available. However, expeditious evaluation of the jaundiced infant that excludes other disorders and determines the biliary anatomy and function, employing nuclear, ultrasonographic, magnetic resonance, or other modalities, may lead to earlier referral for the appropriate operative intervention, the Kasai procedure. When successful, this procedure may delay or forestall the need for liver transplantation and its attendant morbidity. Improvements in the future may come from venues such as improved diagnostic techniques, determination of causes, better operative technique (including the application of robotics), and refinements in transplantation.
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页码:243 / 248
页数:6
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