| Literature DB >> 30317204 |
Sadhana Shankar1,2, Ashwin Rammohan1,2, Srinivas Mettu Reddy1,2, Mohamed Rela1,2,3.
Abstract
Liver transplantation for biliary atresia splenic malformation syndrome associated with situs inversus totalis is a challenging task due to the complexity of associated malformations and the technical proficiency required to overcome them. We present the case of a 6-month-old infant who underwent liver transplantation for biliary atresia. A reduced left lateral segment liver graft from a live donor (his mother) was implanted. The postoperative period was uneventful, and the child remained well on follow-up. Thus, such rare congenital anomalies no longer prove to be a deterrent for successful liver transplantation. © BMJ Publishing Group Limited 2018. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: paediatric surgery; transplantation
Mesh:
Year: 2018 PMID: 30317204 PMCID: PMC6194450 DOI: 10.1136/bcr-2018-226222
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X