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Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease

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[Primary sclerosing cholangitis].

Holmfridur Helgadottir¹, Trine Folseraas², Gunter Kemmerich³

¹Norsk senter for PSC, Avdeling for transplantasjonsmedisin, Klinikk for kirurgi, inflammasjonsmedisin og transplantasjon, Oslo universitetssykehus, Rikshospitalet, og, Medisinsk avdeling, Haraldsplass Diakonale Sykehus.

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|November 21, 2023

Summary

This summary is machine-generated.

Primary sclerosing cholangitis (PSC) is a serious liver condition. This review covers updated guidelines for diagnosing, monitoring, and treating PSC patients, focusing on symptom management and cancer surveillance.

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Area of Science:

Hepatology
Gastroenterology

Background:

Primary sclerosing cholangitis (PSC) is a severe cholestatic liver disease.
It is a leading indication for liver transplantation in Scandinavia.
Early diagnosis and management are crucial for patient outcomes.

Conclusions:

Adherence to updated guidelines is essential for optimal PSC patient care.
Comprehensive management includes symptom control, fibrosis assessment, and vigilant cancer screening.
Multidisciplinary care is vital for patients with primary sclerosing cholangitis.