ATRESIA DE VIAS BILIARES PDF

Introduction: Biliary atresia is the main cause of death by hepatic failure and the main indication for liver transplant in children. Material and methods: Descriptive, observational, and retrospective study, including the patients with biliary atresia, diagnosed and treated between January 1, and December 31, We analyzed epidemiologic, clinical, biochemical, and image data, as well as registered complications and present status. Results: Eighteen patients were evaluated. The median age at time of Kasai portoenterostomy was 63 days of life, with better prognosis for those patients who had surgery before 72 days.

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Initial response to portoenterostomy determines long-term outcome in patients with biliary atresia. Impact of age at Kasai operation on its results in late childhood and adolescence: a rational basis for biliary atresia screening. Is the Kasai operation still indicated in children older than 3 months diagnosed with biliary atresia?

Kasai operation in the age of liver transplantation. Healing or merely palliative technique? Cir Pediatr. Outcome in adulthood of biliary atresia: a study of 63 patients who survived over 20 years with their native liver.

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Universal screening for biliary atresia using an infant stool color card in Taiwan. Biliary atresia: the Brazilian experience. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Services on Demand Journal. Carlos Gomes, cj. How to cite this article.

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Biliary Atresia - Clinical Series

Colestasis neonatal e infantil. Universidad de Los Andes. Universidad Nacional de Colombia. La incidencia de colestasis neonatal es de aproximadamente 1 de cada 2. En la tabla 2 se resume el comportamiento HNI. Es inusual en adultos. Su incidencia es de 1 por cada 2.

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Atresia das vias biliares

Reporte de caso. Biliary atresia is an obstructive neonatal cholangiopathy of unknown etiology that produces damage to the parenchyma of the liver and to the intrahepatic and extrahepatic bile ducts. It is the most common cause of neonatal cholestasis and liver transplantation in the pediatric population. In most cases it manifests as an isolated malformation. This article presents the case of a 75 day old patient with biliary atresia associated with abdominal heterotaxy. Biliary atresia syndrome together with splenic malformation has been previously described, as have biliary atresia associated with anatomical malformations of the spleen, pancreas, and heart.

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