Gastric Sarcoidosis: A Rare Clinical Presentation

Joint Authors

Polsani, Karthik
Kalavakunta, Jagadeesh Kumar
Tokala, Hemasri

Source

Case Reports in Gastrointestinal Medicine

Issue

Vol. 2013, Issue 2013 (31 Dec. 2013), pp.1-3, 3 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2013-12-04

Country of Publication

Egypt

No. of Pages

3

Main Subjects

Diseases

Abstract EN

Gastrointestinal (GI) sarcoidosis is a very rare disease, which clinically presents along with systemic disease or as an isolated finding.

Gastric sarcoidosis is the most common form of GI sarcoidosis.

Symptomatic gastric sarcoidosis is rare and only few case reports have been described in the literature with well-documented histological evidence of noncaseating granulomas.

We present an interesting case of gastric sarcoidosis in a 39-year-old Caucasian man with symptoms of epigastric pain and profound weight loss.

His endoscopic gastric mucosal biopsies revealed noncaseating granulomas consistent with gastric sarcoidosis.

Treatment with oral steroids alleviated his symptoms with no recurrence in 2 years.

Gastric sarcoidosis should be considered in patients with history of sarcoidosis and GI symptoms.

American Psychological Association (APA)

Tokala, Hemasri& Polsani, Karthik& Kalavakunta, Jagadeesh Kumar. 2013. Gastric Sarcoidosis: A Rare Clinical Presentation. Case Reports in Gastrointestinal Medicine،Vol. 2013, no. 2013, pp.1-3.
https://search.emarefa.net/detail/BIM-1005678

Modern Language Association (MLA)

Tokala, Hemasri…[et al.]. Gastric Sarcoidosis: A Rare Clinical Presentation. Case Reports in Gastrointestinal Medicine No. 2013 (2013), pp.1-3.
https://search.emarefa.net/detail/BIM-1005678

American Medical Association (AMA)

Tokala, Hemasri& Polsani, Karthik& Kalavakunta, Jagadeesh Kumar. Gastric Sarcoidosis: A Rare Clinical Presentation. Case Reports in Gastrointestinal Medicine. 2013. Vol. 2013, no. 2013, pp.1-3.
https://search.emarefa.net/detail/BIM-1005678

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-1005678