Seven patients with situs inversus abdominis and one with situs invers
us totalis underwent liver transplantation; all are alive at follow-up
of between 7 months and 5 years. Two patients required retransplantat
ion within the first 3 weeks (for primary non-function and thrombotic
infarction). Seven had additional abnormalities associated with the po
lysplenia-biliary atresia syndrome. Liver transplantation in these pat
ients involved selection of relatively small donor organs or use of re
duced-sized grafts. Delay abdominal wall closure was necessary in two
patients and all required a modification of the 'piggy-back' technique
of suprahepatic vena caval anastomosis to overcome recipient venous a
nomalies. Biliary drainage by Roux-en-Y choledochojejunostomy was the
preferred technique. Although technically challenging, situ inversus i
s not a contraindication to liver transplantation and patients should
expect full recovery.