An overview of the Kasai operation for biliary atresia
نویسندگان
چکیده
منابع مشابه
A 25 years old women after Kasai operation for biliary atresia.
Manuscript received and accepted: 2 August and 15 September 2008 Biliary atresia is a rare disease characterized by a biliary obstruction of unknown origin that presents in the neonatal period. We present the magnetic resonance cholangiography (MRC) from a 25 years old women who was treated in the neonatal period with Kasai operation. The MRC reveals a choledochal cyst and shows multiple saccul...
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children who are operated for biliary atresia by the kasai procedure have approximately 30% chance of survival for 5 years. in an attempt to define the role of this operation for biliary atresia, the surgery records of the past 15 years were reviewed. the aim of this study was to assess the benefits achieved from this operation in infants with biliary atresia. this study was conducted in the de...
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Biliary atresia is a rare neonatal disease of unknown etiology, where obstruction of the biliary tree causes severe cholestasis, leading to biliary cirrhosis and death in the first years of life, if the condition is left untreated. Biliary atresia is the most frequent surgical cause of cholestatic jaundice in neonates and should be evoked whenever this clinical sign is associated with pale stoo...
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Portoenterostomy (PE) is the standard therapy for biliary atresia (BA). PE offers the chance of survival to children with BA. PE was the ultimate therapeutic modality for BA before liver transplantation (LT) was available. Failure of biliary drainage with PE was almost invariably fatal in children with BA. In such cases, redo-PE was performed to salvage patients following PE failure. PE remains...
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ژورنال
عنوان ژورنال: Gastroenterology
سال: 1978
ISSN: 0016-5085
DOI: 10.1016/0016-5085(78)90597-8