Pediatric split liver transplantation after Fontan procedure in left isomerism combined with biliary atresia: a case report

Pediatr Transplant. 2014 Dec;18(8):E274-9. doi: 10.1111/petr.12364. Epub 2014 Sep 27.

Abstract

LI is a subset of the heterotaxy syndrome and a rare birth defect that involves the heart and other organs. It can be combined with extracardiac abnormalities, especially BA. CHD can be associated with LI in up to 15% of cases, although it is rare in BA. Pediatric LT for a child with ESLD due to BA combined with LI and CHD is a challenging issue for a transplant surgeon. Herein, we report a successful split LT on a three-yr-old boy with LI who survived after a Fontan procedure due to single ventricle, but who suffered from HPS associated with BA.

Keywords: Fontan operation; biliary atresia; hepatopulmonary syndrome; left isomerism; liver transplantation.

Publication types

  • Case Reports

MeSH terms

  • Biliary Atresia / complications
  • Biliary Atresia / surgery*
  • Child, Preschool
  • Fontan Procedure*
  • Hepatopulmonary Syndrome / etiology
  • Hepatopulmonary Syndrome / surgery
  • Heterotaxy Syndrome / surgery*
  • Humans
  • Liver Transplantation / methods*
  • Male