[Prognostic factors related to mortality of children with atresia of bile ducts]. Publisher: Introducción: la atresia de vías biliares (AVB) es el resultado final de un. Atresia de vías biliares vs. Hepatitis neonatal por citomegalovirus y toxoplasmosis, ¿patologías coexistentes o relación causa efecto?. Biliary Atresia – Clinical Series. Atresia das Vias Biliares – Revisão Casuística. Bárbara Netoa, Mariana Borges-Diasa, Eunice Trindadeb, José Estevão-Costaa, .

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[Prognostic factors related to mortality of children with atresia of bile ducts].

However, the definitive diagnosis is confirmed only by exploratory surgery [1] Fig. Among those patients who had other associated malformations 5only one needed liver transplant. KPthe age at delivery was 4.

Services on Demand Journal. The biliary atresia BA is the end result of a destructive and idiopathic inflammatory process affecting the intrahepatic and extrahepatic bile ducts, leading to fibrosis and biliary cirrhosis. This difference is probably related to the short follow-up time of some of the studied patients, in whom portal hypertension may be documented in voas future.

[Prognostic factors related to mortality of children with atresia of bile ducts].

A population-based study on the incidence and possible pre-and perinatal etiologic risk factors of biliary atresia. Pediatric gastrointestinal disease, 3rd ed, pp. Portal hypertension in children and young adults with biliary atresia. Lancet,pp. Pediatr Clin North Am, 35pp.


Atresia das Vias Biliares: Revisão Casuística

J Pediatr Gastroenterol Nutr, 16pp. The study population was characterized according to the following parameters: In order to calculate the postoperative native liver survival rates, Kaplan-Meier method was used, assuming it started at the time of Kasai PE and ended at the time of death viass hepatic transplant. Epidemiology of atrdsia atresia: SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.

Future research into the role of interferon-gamma and of other cytokines is necessary in order to assess whether these aspects should be potential targets for therapeutic intervention.

Gastrointest Endosc, 37pp. Potential errors in the diagnosis and surgical management of neonatal jaundice.

There was a positive relation, with statistical significance, to native liver survival in patients who were submitted to surgery atrssia 72 days of life, which supports the data referred to in other studies. Eur J Pediatr Surg, 8pp. Disclosure Statement The authors have no conflicts of interest to declare. A new diagnostic approach to biliary atresia with emphasis on the ultrasonographic triangular cord sign: Foram avaliados 18 doentes.


However, there was a higher surgical success and survival rates at 5 and 10 years of follow-up than most series. Hospital Infantil La Fe. Annals of Pediatrics is the Body of Scientific Expression of the Association and is the vehicle through which members communicate.

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Full text is only aviable in PDF. Life after portoenterostomy in biliary atresia. Liver, 22pp.

Atypical morphologic presentation of biliary atresia vais value of serial liver biopsies. There was a significant association between recurrent cholangitis and survival.

There was only one case in which the exploratory surgery did not confirm the diagnosis of biliary atresia. Gamma-glutamyl transpeptidase activity and its serial measurament in differentation between extrahepatic biliary atresia and neonatal hepatitis.