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Biliar atresia

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https://www.readbyqxmd.com/read/16671510/-choledocal-cyst-analysis-of-29-cases-and-review-or-the-literature
#1
REVIEW
J J Vila-Carbó, L Ayuso, E Hernández, J Lluna, V Ibáñez
UNLABELLED: The aim of the present study has been to systematize the clinical presentation of the entity named choledochal cyst, in relation with its probable etiopathology and the intraoperative findings as well as its evolution after surgery, based on the revision of the literature and of our experience in 29 cases. MATERIAL AND METHODS: 29 cases of cystic dilatation of the biliar duct extra and/or intrahepatic are analyzed. In 4 cases the diagnosis was prenatal and two were excluded of the study after it has been confirmed they suffered biliary atresia type I...
January 2006: Cirugía Pediátrica: Organo Oficial de la Sociedad Española de Cirugía Pediátrica
https://www.readbyqxmd.com/read/13721349/-congenital-atresia-of-the-biliary-tract
#2
D DEL HIGADO, V BILIARES
No abstract text is available yet for this article.
February 1961: Acta Pediátrica Española
https://www.readbyqxmd.com/read/12601939/-bile-duct-atresia-outline-for-a-solution
#3
J Broto, M Asensio, J M Gil Vernet, C Marhuenda, J Boix Ochoa
UNLABELLED: Biliary atresia continues to be a serious and relatively rare disease (1/50,000 newborns) and whose long-term prognosis has changed drastically since the appearance of liver transplant (LT) as a therapeutic weapon. The combination of two factors, early diagnosis and correct application of Kasai's surgical technique, is essential to obtain acceptable results and sufficient biliary drainage allowing the children to overcome the critical 7 kg barrier and place them in the lesser morbi-mortality range in relation to a possible LT...
July 2000: Cirugía Pediátrica: Organo Oficial de la Sociedad Española de Cirugía Pediátrica
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