| Literature DB >> 25343066 |
Sumihito Tamura1, Yasuhiko Sugawara1, Norihiro Kokudo1.
Abstract
Primary sclerosing cholangitis (PSC) is a chronic cholestatic liver disease of unknown origin which eventually results in liver cirrhosis. The disease is reported to be more common among the Western population than in the Asian population. Asian experience remains limited. Diagnosis and treatment standards in the Far East have largely followed those in the West, including liver transplantation. Unlike in the West, however, recent reports from Japan have presented with a higher recurrence rate of PSC after liver transplantation, suggesting the intractable nature of the disease even after the replacement of the entire affected organ.Entities:
Keywords: Japan; Primary sclerosing cholangitis (PSC); deceased donor liver transplantation (DDLT); living donor liver transplantation (LDLT)
Year: 2012 PMID: 25343066 PMCID: PMC4204589 DOI: 10.5582/irdr.2012.v1.1.13
Source DB: PubMed Journal: Intractable Rare Dis Res ISSN: 2186-3644