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Congenital absence of the portal vein: Define the portosystemic shunt, avoid liver transplantation.
Laverdure, Noémie; Lallier, Michel; Dubois, Josée; Paganelli, Massimiliano.
Afiliación
  • Laverdure N; Pediatric Gastroenterology Hepatology and Nutrition, CHU Sainte-Justine, Université de Montréal, Montréal, Québec, Canada.
  • Lallier M; Service d'Hépato-gastroenterologie et nutrition pediatrique, Hopital Femme Mere Enfant, Lyon, France.
  • Dubois J; Pediatric Surgery, CHU Sainte-Justine, Université de Montréal, Montréal, Québec, Canada.
  • Paganelli M; Pediatric Radiology, CHU Sainte-Justine, Université de Montréal, Montréal, Québec, Canada.
Can Liver J ; 4(3): 322-327, 2021.
Article en En | MEDLINE | ID: mdl-35992262
Liver transplantation has been historically recommended for patients with congenital absence of the portal vein associated with extrahepatic congenital portosystemic shunts. Here, based on a case report of a 2-year-old girl and a thorough review of all published cases from 1974 to 2020, we show that such a diagnosis most often conceals a hypoplastic portal vein, which can be successfully re-permeabilized through the closure of the shunt in order to re-establish a physiological vascular anatomy. This highlights the importance of achieving a detailed anatomical description of extrahepatic congenital portosystemic shunts with a balloon occlusion test in order to plan the best surgical approach and avoid unnecessary liver transplantation.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Can Liver J Año: 2021 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Can Liver J Año: 2021 Tipo del documento: Article País de afiliación: Canadá