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- W3089607481 endingPage "364" @default.
- W3089607481 startingPage "337" @default.
- W3089607481 abstract "Cholestatic liver diseases include a wide variety of entities, characterized by impaired hepatobiliary production and excretion of bile, leading to cholestasis. Primary biliary cirrhosis (PBC) and primary sclerosing cholangitis (PSC) are the two most common chronic cholestatic liver diseases, caused by immune-mediated cholangiocytes injury, through a complex interaction with environmental factors. PBC is characterized by small bile duct lymphocytic cholangitis occurring mainly in women, with a good response to ursodeoxycholic acid. PSC is characterized by inflammation, fibrosis, and stricture of the large bile ducts, affecting young men, still without effective therapy. Besides PBC and PSC, cholestatic liver diseases include also secondary sclerosing cholangitis with identifiable causes of bile duct injury. Secondary sclerosing cholangitis is large group of diseases which include immunoglobulin G4-related sclerosing disease, recurrent pyogenic cholangitis, ischemic cholangitis, acquired immunodeficiency syndrome-related cholangitis, and eosinophilic cholangitis. In addition to clinical and laboratory findings, the recognition of typical imaging features on computed tomography and magnetic resonance (MR) imaging with MR cholangiography is essential for differential diagnosis among cholestatic liver diseases." @default.
- W3089607481 created "2020-10-08" @default.
- W3089607481 creator A5062489819 @default.
- W3089607481 date "2020-09-29" @default.
- W3089607481 modified "2023-10-17" @default.
- W3089607481 title "Non-tumoral Pathology of the Intrahepatic Biliary Tract" @default.
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