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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.
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页码:208 / 212
页数:5
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