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Best Pract Res Clin Gastroenterol. 2011 Dec;25(6):701-12. doi: 10.1016/j.bpg.2011.10.005.

Diagnosis of primary biliary cirrhosis.

Author information

1
Department of Medicine, University of Toronto, Canada. gideon.hirschfield@uhn.on.ca

Abstract

Primary biliary cirrhosis is the archetypal autoimmune liver disease, with the disease label describing a chronic granulomatous lymphocytic small bile duct cholangitis, which now most commonly presents asymptomatically and at an early pre-cirrhotic stage. Disease is more common than thought, with 1 in 1000 women over the age of 40 affected. Characteristic immunologic features of the disease assist clinicians in ready non-invasive diagnosis of patients, even if asymptomatic with only anicteric/cholestatic liver biochemical profiles. Over 90% of patients are anti-mitochondrial antibody positive, and for those negative, a significant proportion have highly specific anti-nuclear antibody profiles. Liver biopsy remains useful in certain settings where clarity is needed to confirm diagnosis, exclude alternative disease, and assess the relative contribution of PBC to other co-existent liver injury, and seeks to demonstrate in particular the classic bile duct lesions, as well as the degree of interface activity.

PMID:
22117636
DOI:
10.1016/j.bpg.2011.10.005
[Indexed for MEDLINE]

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