Living donor liver transplantation for biliary atresia complicated by situs inversus: Technical highlights
Kentaro Matsubara, Yasuhiro Fujimoto, Hideya Kamei, Kohei Ogawa, Mureo Kasahara, Mikiko Ueda, Hiroto Egawa, Yasutsugu Takada, Masaki Kitajama, Koichi Tanaka – 19 October 2005 – Living‐donor liver transplantation (LDLT) has become an established technique to treat children with end‐stage liver disease. Biliary atresia (BA), one of the most common indications for liver transplantation in children, can be associated with situs inversus (SI). In the past, the presence of SI has been considered to be an absolute contraindication for liver transplantation because of the technical difficulties.