| Literature DB >> 27659790 |
Antoine Bruneau1, Giovanni Battista Levi Sandri1, Michel Rayar1, Laurent Sulpice1, Karim Boudjema2,3.
Abstract
Wandering liver syndrome is an extremely rare congenital disorder. It is mainly diagnosed within the first years of life. Herein we report the case of a 40-year-old woman with hepatoptosis due to the absence of anatomical peritoneal attachments of the liver. Surgical treatment consisted in inserting the floppy right lobe of the liver in a subphrenic retroperitoneal pouch. This original technique provided excellent postoperative result.Entities:
Keywords: Hepatoptosis; Liver surgery; Wandering liver
Mesh:
Year: 2016 PMID: 27659790 DOI: 10.1007/s11605-016-3277-x
Source DB: PubMed Journal: J Gastrointest Surg ISSN: 1091-255X Impact factor: 3.452