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dc.contributor.authorYonem, Ozlem
dc.contributor.authorBayraktar, Yusuf
dc.date.accessioned2019-12-10T11:10:52Z
dc.date.available2019-12-10T11:10:52Z
dc.date.issued2007
dc.identifier.issn1007-9327
dc.identifier.urihttps://doi.org/10.3748/wjg.v13.i13.1930
dc.identifier.urihttp://hdl.handle.net/11655/14923
dc.description.abstractCaroli's disease is a rare congenital condition characterized by non-obstructive saccular or fusiform dilatation of larger intrahepatic bile ducts. Cholangitis, liver cirrhosis, and cholangiocarcinoma are its potential complications. The diagnosis of Caroli's disease depends on demonstrating that the cystic lesions are in continuity with the biliary tree which can be showed by ultrasonography, computerized tomography, endoscopic retrograde cholangiopancreatography, percutaneous transhepatic cholangiography or magnetic resonance cholangiopancreatography. Treatment of Caroli's disease relies on the location of the biliary abnormalities. While localized forms confined to one lobe can be treated with surgery, liver transplantation is the only effective modality for diffuse forms. Although a rare disorder; Caroli's disease should always be considered in the differential diagnosis of chronic cholestasis of unknown cause. (C) 2007 The WJG Press. All rights reserved.
dc.language.isoen
dc.publisherW J G Press
dc.relation.isversionof10.3748/wjg.v13.i13.1930
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectGastroenterology & Hepatology
dc.titleClinical Characteristics Of Caroli'S Disease
dc.typeinfo:eu-repo/semantics/article
dc.relation.journalWorld Journal Of Gastroenterology
dc.contributor.departmentİç Hastalıkları
dc.identifier.volume13
dc.identifier.issue13
dc.identifier.startpage1930
dc.identifier.endpage1933
dc.description.indexWoS


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