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Published in: Pediatric Rheumatology 1/2015

Open Access 01-12-2015 | Case Report

Intestinal malrotation as a misdiagnosis of pediatric colchicine resistant familial Mediterranean fever

Authors: Merav Heshin-Bekenstein, Philip J. Hashkes

Published in: Pediatric Rheumatology | Issue 1/2015

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Abstract

Background

Familial Mediterranean fever (FMF) is a disorder characterized by recurrent attacks of fever and serosal inflammation, particularly abdominal pain. Other disease processes, including medical and surgical emergencies, may mimic FMF, especially in atypical cases.

Case Presentation

We present a case of an adolescent male, referred to us with a diagnosis of colchicine resistant FMF, ultimately diagnosed with intestinal malrotation and recurrent volvulus.

Conclusions

In atypical presentations of FMF with potential “red flags”, a thorough patient history is extremely important and should result in prompt referral for the appropriate diagnostic tests.
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Metadata
Title
Intestinal malrotation as a misdiagnosis of pediatric colchicine resistant familial Mediterranean fever
Authors
Merav Heshin-Bekenstein
Philip J. Hashkes
Publication date
01-12-2015
Publisher
BioMed Central
Published in
Pediatric Rheumatology / Issue 1/2015
Electronic ISSN: 1546-0096
DOI
https://doi.org/10.1186/s12969-015-0044-6

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