Primary sclerosing cholangitis

被引:48
作者
Karlsen, Tom H. [1 ]
Schrumpf, Erik [1 ]
Boberg, Kirsten Muri [1 ]
机构
[1] Natl Hosp Norway, Oslo Univ Hosp, Clin Specialized Med & Surg, Norwegian PSC Res Ctr, N-0027 Oslo, Norway
关键词
Primary sclerosing cholangitis; Genetic predisposition; Disease progression; Co-morbidities; Treatment; INFLAMMATORY-BOWEL-DISEASE; DOSE URSODEOXYCHOLIC ACID; GENOME-WIDE ASSOCIATION; POUCH-ANAL ANASTOMOSIS; LIVER-TRANSPLANTATION; ULCERATIVE-COLITIS; RISK-FACTORS; DOMINANT STRICTURES; NATURAL-HISTORY; COLORECTAL NEOPLASIA;
D O I
10.1016/j.bpg.2010.07.005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Primary sclerosing cholangitis (PSC) is a chronic bile duct disease leading to fibrotic biliary strictures and liver cirrhosis The patient population is heterogeneous with regard to disease progression and the presence of co-morbidities complicating the practical handling of patients as well as studies of pathogenetic mechanisms The aetiology of PSC is unknown but the recent findings of several robust susceptibility genes emphasise the importance of genetic risk factors There is no effective medical treatment available to delay the disease progression but endoscopic therapy of biliary stenoses may be indicated Follow-up of patients includes management of the inflammatory bowel disease that is found in the majority of cases along with investigations aimed at the early detection of cholangiocarcinoma and colorectal cancer which also occur at increased frequencies In the present review we aim to summarise the present knowledge of PSC with a particular emphasis on the possible basis of disease variability (C) 2010 Elsevier Ltd All rights reserved
引用
收藏
页码:655 / 666
页数:12
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