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How can portal vein cavernous transformation cause chronic incomplete biliary obstruction?

Abstract

Biliary disease in the setting of non-cirrhotic portal vein thrombosis (and similarly in portal vein cavernous transformation) can become a serious problem during the evolution of disease. This is mostly due to portal biliary ductopathy. There are several mechanisms that play a role in the development of portal biliary ductopathy, such as induction of fibrosis in the biliary tract (due to direct action of dilated peribiliary collaterals and/or recurrent cholangitis), loss of biliary motility, chronic cholestasis (due to fibrosis or choledocholithiasis) and increased formation of cholelithiasis (due to various factors). The management of cholelithiasis in cases with portal vein cavernous transformation merits special attention. Because of a heterogeneous clinical presentation and concomitant pathophysiological changes that take place in biliary anatomy, diagnosis and therapy can become very complicated. Due to increased incidence and complications of cholelithiasis, standard treatment modalities like sphincterotomy or balloon sweeping of bile ducts can cause serious problems. Cholangitis, biliary strictures and hemobilia are the most common complications that occur during management of these patients. In this review, we specifically discuss important issues about bile stones related to bile duct obstruction in non-cirrhotic portal vein thrombosis and present evidence in the current literature.

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  • Authors

    Harmanci O, Bayraktar Y

    Institution

    Department of Medicine, Division of Gastroenterology, Faculty of Medicine, Hacettepe University, 06100 Ankara, Turkey. ozgurmd@hacettepe.edu.tr

    Source

    World journal of gastroenterology : WJG 18:26 2012 Jul 14 pg 3375-8

    MeSH

    Animals
    Bile
    Bile Ducts
    Biliary Tract Diseases
    Cholelithiasis
    Cholestasis
    Fibrosis
    Gallbladder
    Hemobilia
    Humans
    Portal Vein
    Recurrence
    Ultrasonography

    Pub Type(s)

    Journal Article
    Review

    Language

    eng

    PubMed ID

    22807606