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Primary sclerosing cholangitis: review for radiologists.
Matthew A Morgan1, Rachita Khot2, Karthik M Sundaram3
1Department of Radiology, University of Pennsylvania Health System, 1 Silverstein, 3400 Spruce Street, Philadelphia, PA, USA. Matthew.Morgan@pennmedicine.upenn.edu.
Abdominal Radiology (New York)
|September 5, 2022
Summary
Primary sclerosing cholangitis (PSC) is a rare bile duct disease causing strictures and cirrhosis. This review details PSC
Area of Science:
- Gastroenterology and Hepatology
- Radiology
- Immunology
Background:
- Primary sclerosing cholangitis (PSC) is a rare, chronic inflammatory bile duct disease.
- It can lead to bile duct strictures, cholestasis, and cirrhosis.
- Patients may be asymptomatic or present with cholestasis symptoms.
Purpose of the Study:
- To provide a comprehensive review of primary sclerosing cholangitis.
- To cover its pathophysiology, clinical features, and imaging findings.
- To discuss surveillance methods and post-transplant appearance.
Main Methods:
- Literature review of primary sclerosing cholangitis.
- Synthesis of information on pathophysiology, clinical presentation, and imaging.
- Inclusion of data on surveillance and post-transplant management.
Main Results:
- PSC involves chronic inflammation leading to bile duct damage.
- Clinical presentation varies from asymptomatic to cholestatic symptoms.
- Imaging is crucial for diagnosis and monitoring disease progression.
Conclusions:
- Primary sclerosing cholangitis requires a multidisciplinary approach.
- Understanding imaging findings is key for diagnosis and management.
- Surveillance and post-transplant care are important aspects of PSC management.
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