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Updated: Oct 26, 2025

Partial Bile Duct Ligation in the Mouse: A Controlled Model of Localized Obstructive Cholestasis
Published on: March 28, 2018
Non-invasive diagnosis and follow-up of primary biliary cholangitis
Christophe Corpechot1, Alexandra Heurgue2, Florence Tanne3
1Service d'hépato-gastroentérologie, Hôpital Saint Antoine, APHP, Paris, France; Reference centre for inflammatory biliary diseases and autoimmune hepatitis (MIVB-H), French network for rare liver diseases in children and adults (FILFOIE), European Reference Network on Rare Hepatological Diseases (ERN RARE-LIVER), Inserm UMR_S938, Saint-Antoine Research Center (CRSA), Université de Paris Sorbonne, France.
Abstract:
Primary biliary cholangitis (PBC) is a chronic inflammatory disease of the intra-hepatic bile ducts [1]. It is characterised biologically by chronic cholestasis associated with the presence of specific autoantibodies, and histologically by lesions of nonsuppurative destructive cholangitis. If left untreated it can progress to cirrhosis, portal hypertension and liver failure. Diagnosis, staging and follow-up are largely based on non- or minimally-invasive assessment (blood tests, ultrasound, liver stiffness measurement). Histological examination of the liver and upper gastrointestinal endoscopy are sometimes necessary, but their indications remain limited. The purpose of this chapter is to provide the clinicians with what should be known about the non-invasive assessment of PBC and to provide specific recommendations for clinical practice.
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