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Gastrointestinal sarcoidosis. A review
Matthew Adler1, Andrew Burroughs, Huw Beynon
1Department of Rheumatology, Royal Free Hospital, London, UK. matthew.adler@hwph-tr.nhs.uk
Gastrointestinal sarcoidosis is rare and often asymptomatic, complicating diagnosis. This review covers its manifestations, diagnostic challenges, and treatment options, including biologic therapies.
Area of Science:
- Gastroenterology
- Immunology
- Internal Medicine
Background:
- Sarcoidosis is a multisystem granulomatous disease.
- Gastrointestinal involvement is uncommon, often asymptomatic, but can cause significant morbidity and mortality.
- Hepatobiliary manifestations also occur.
Purpose of the Study:
- To review common and rare gastrointestinal and hepatobiliary manifestations of sarcoidosis.
- To discuss diagnostic difficulties and differential diagnoses.
- To outline treatment options, including novel therapies.
Main Methods:
- Comprehensive literature search of Pubmed from 1966 to 2006.
- Keywords: 'Gastrointestinal', 'Hepatobiliary', 'Sarcoidosis'.
Main Results:
- Review covers all sections of the gastrointestinal and hepatobiliary tracts.
- Highlights challenges in diagnosis due to asymptomatic nature and mimicry of other diseases.
- Discusses treatment strategies and disease associations.
Conclusions:
- Establishing a diagnosis of gastrointestinal sarcoidosis is challenging.
- Mimics other non-caseating granulomatous diseases.
- Biologic therapies show promise in managing sarcoidosis and associated biliary disorders.
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