Small-duct primary sclerosing cholangitis with hepatocellular carcinoma requiring liver transplantation

被引:0
|
作者
Sharif Ali [1 ]
Veena Shah [1 ]
机构
[1] Department of Pathology and Laboratory Medicine,Henry Ford Health System
关键词
primary sclerosing cholangitis; small-duct diseases of the liver; hepatocellular carcinoma; liver transplantation;
D O I
暂无
中图分类号
R735.7 [肝肿瘤]; R657.4 [胆囊、胆管];
学科分类号
1002 ; 100210 ; 100214 ;
摘要
BACKGROUND:Primary sclerosing cholangitis(PSC)is a chronic progressive cholestatic liver disease,which usually affects young adults and is diagnosed by cholangiography.On a few occasions,the disease either starts in or exclusively involves the small intrahepatic bile ducts,referred to as small-duct PSC. METHODS:A 31-year-old man presented with severe hematemesis secondary to liver cirrhosis.Over a course of 8 years,his liver decompensated and required an orthotopic liver transplantation. In this report we discuss his disease presentation,course of management,and the post-transplantation course of manage- ment,and review the morphologic diagnosis,and differential diagnosis of the disease with large-duct type and other diseases that involve small intrahepatic bile ducts. RESULTS:The patient’s explanted liver showed changes of PSC affecting only the small-and medium-sized bile ducts in addition to three incidental nodules of hepatocellular carcinoma. CONCLUSIONS:Small-duct PSC has a substantially better prognosis than the large-duct type,with less chance of developing cirrhosis and an equal risk for developing hepato- cellular carcinoma,but no increased risk for developing cholangiocarcinoma.Treatment seems to help relieve the symptoms but not necessarily improve survival.Liver transplantation remains the ultimate cure.
引用
收藏
页码:208 / 212
页数:5
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