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Short communication, Note

Primary Biliary Cholangitis – Case Report and Review of Literature

Ivana Mikolašević
Nadija Skenderević


Full text: croatian pdf 117 Kb

page 89-94

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Full text: english pdf 117 Kb

page 89-89

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Abstract

Primary biliary cirrhosis (PBC), also known as primary biliary cholangitis, is an autoimmune disorder that belongs to the group of cholestatic liver diseases. PBC is a chronic inflammatory liver disease that can lead to liver fibrosis and cirrhosis and the development of hepatocellular carcinoma. Understanding the biology of PBC is important to ensure effective patient care, improve therapeutic options and provide targeted treatment. PBC is typically a disease that requires lifelong therapy aimed at preventing the progression of the liver disease and at reducing or eliminating the symptoms that impair patients’ quality of life. In everyday clinical practice, PBC should be considered in all patients with elevated cholestasis parameters, especially if they last longer than 6 months. The paper presents a case of a female patient suffering from PBC with a persistent diagnosis and demanding treatment.

Keywords

primary biliary cirrhosis; cholestasis; therapy

Hrčak ID:

232205

URI

https://hrcak.srce.hr/232205

Publication date:

15.1.2020.

Article data in other languages: croatian

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