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A case of intestinal amoebiasis mimicking intestinal Behçet's disease.

Authors :
Fukui A
Nakayama Y
Yoshida T
Murakami K
Kadoba K
Onizawa H
Akizuki S
Nakashima R
Yoshifuji H
Ohmura K
Sugimoto A
Yamamoto S
Morinobu A
Source :
Modern rheumatology case reports [Mod Rheumatol Case Rep] 2022 Jun 24; Vol. 6 (2), pp. 270-272.
Publication Year :
2022

Abstract

Intestinal amoebiasis is caused by Entamoeba histolytica (E. histolytica) and is characterised by cecal lesions, multiple lesions, aphthae, and multiple exudative erosions. Intestinal Behçet's disease (BD) is a chronic inflammatory disorder that is characterised by multiple ulcers. Although the aetiologies of these two bowel diseases are unrelated, they are difficult to distinguish because they present similarly with inflammation and ulcers, especially if evidence of specific pathogens is not detected. Herein, we report a case of intestinal amoebiasis in a patient with BD. The patient underwent colonoscopy four times before intestinal amoebiasis was diagnosed. As intestinal BD was initially suspected, she received high-dose glucocorticoid therapy, which exacerbated her condition. Following exacerbation, she underwent colonoscopy, and E. histolytica was revealed. Deliberate care should be taken to distinguish between intestinal amoebiasis and intestinal BD, as the appropriate treatments for these diseases are entirely different.<br /> (© Japan College of Rheumatology 2022. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)

Details

Language :
English
ISSN :
2472-5625
Volume :
6
Issue :
2
Database :
MEDLINE
Journal :
Modern rheumatology case reports
Publication Type :
Academic Journal
Accession number :
35388431
Full Text :
https://doi.org/10.1093/mrcr/rxac028