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Primary Biliary Cholangitis – Case Report and Review of Literature

Ivana Mikolašević
Nadija Skenderević


Puni tekst: hrvatski pdf 117 Kb

str. 89-94

preuzimanja: 2.520

citiraj

Puni tekst: engleski pdf 117 Kb

str. 89-89

preuzimanja: 363

citiraj


Sažetak

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.

Ključne riječi

primary biliary cirrhosis; cholestasis; therapy

Hrčak ID:

232205

URI

https://hrcak.srce.hr/232205

Datum izdavanja:

15.1.2020.

Podaci na drugim jezicima: hrvatski

Posjeta: 7.301 *