ATRESIA DE VIAS BILIARES EXTRAHEPATICAS PDF

Atrésia das vias biliares extrahepáticas: estudo clínico retrospectivo. Ermelinda Santos Silva1, Margarida Medina1, Paula Rocha2, Berta Bonet3, J.A. Ferreira. Resumo. Introdução: A atresia das vias biliares representa a princi- pal causa de morte por insuficiência hepática e a principal indicação para. Na atresia das vias biliares ocorre a obliteração ou descontinuidade do sistema biliar extra‐hepático, resultando numa obstrução ao fluxo.

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Ferreira de Sousa 3Carlos Enes 3. Foram atendidos 15 doentes seis em P1 e nove em P2. A sobrevida global aos cinco anos foi To obtain further insight into the natural history of patients with biliary atresia and to determine survival and prognostic wtresia.

This period was divided in two parts: The following variables were analysed: There were 15 patients attended six in P1 and nine in P2. Median time between admission and Kasai procedure was 10 days 14 days in P1; 7days in P2.

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Median age at Kasai procedure was 58 days 89 days in P1; 45 days in P2. Overall ve years survival was Five years survival with native liver was Surgical treatment of biliary atresia. J Pediatr Surg3: Sequencial treatment of biliary atresia with Kasai portoenterostomy and liver transplantation: Hepatology atresiw, 20 1 Pt2: Seamless management of biliary atresia in England and Wales Management of patients with extahepaticas atresia in France: Five and year survival rates after surgery for biliary atresia: J Pediatr Surg ; Outcome in adulthood of biliary atresia: Long term prognosis of patients with biliary atresia: J Pediatr Gastroenterol Nutr ; Prognosis of biliary atresia: J Pediatrics atreia Screening and Outcomes in biliary atresia: Screening for biliary atresia by infant stool color card in Taiwan.

Atrésia das vias biliares extrahepáticas: estudo clínico retrospectivo

Universal screening for biliary atresia using an infant stool color card in Taiwan. British paediatric surveillance unit study of biliary atresia: Epidemiology of biliary atresia in France: Prognosis of biliary atresia in the era of liver transplantation: French national study from to A multicenter study of the outcome of biliary atresia in the United States, to J Pediatr ; Swiss National Study, J Pediatr Gastroenterol Nutr ; 46 3: Treatment of biliary atresia with special reference to hepatic porto-enterostomy and its modifications.

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Prog Pediatr Surg ;6: Acta Pediatr Port ; 41 3: Ferreira de Sousa 3Carlos Enes 3 1 S. Biliary atresia, neonatal cholestasis, liver transplantation. Full text only available in PDF format.

Orphanet J Rare Dis ;1: Abel Salazar Porto nascerecrescer chporto. Como citar este artigo.