| Literature DB >> 35535065 |
Bikrant B Lal1, Vikrant Sood1, Kavita Jain2, Chhagan Bihari2, Rajeev Khanna1, Seema Alam1.
Abstract
The clinical course after liver transplantation (LT) in progressive familial intrahepatic cholestasis type 1 (PFIC1) is complicated by intractable diarrhoea, growth failure, graft steatosis and cirrhosis. Recent evidence from Japan suggests the role of genotype to predict outcome after LT. We report a case with pathogenic frameshift mutation who had failed partial external biliary diversion, underwent LT and his post-LT course has been complicated by intractable diarrhoea, growth failure, steatosis and fibrosis. This case highlights the fact that homozygous frameshift p.Gly197LeufsTer10 mutation in ATP8B1 is associated with poor outcome and genetic evaluation should be mandatory before subjecting the patient to LT.Entities:
Keywords: ESLD, end-stage liver disease; LT, liver transplant; PFIC, progressive familial intrahepatic cholestasis; POD, postoperative day; TPN, total parenteral nutrition; cholestasis; graft biopsy; liver transplantation; progressive familial intrahepatic 1
Year: 2021 PMID: 35535065 PMCID: PMC9077163 DOI: 10.1016/j.jceh.2021.06.009
Source DB: PubMed Journal: J Clin Exp Hepatol ISSN: 0973-6883