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Familial Mediterranean fever in which Crohn’s disease was suspected: a case report
BACKGROUND: Familial Mediterranean fever is a hereditary autoinflammatory disease, mainly characterized by periodic fever and serositis. The level of awareness about familial Mediterranean fever is far from sufficient, and it is assumed that there may be many patients with this disease who are under...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4182779/ https://www.ncbi.nlm.nih.gov/pubmed/25261084 http://dx.doi.org/10.1186/1756-0500-7-678 |
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author | Matsumoto, Satohiro Urayoshi, Shunsuke Yoshida, Yukio |
author_facet | Matsumoto, Satohiro Urayoshi, Shunsuke Yoshida, Yukio |
author_sort | Matsumoto, Satohiro |
collection | PubMed |
description | BACKGROUND: Familial Mediterranean fever is a hereditary autoinflammatory disease, mainly characterized by periodic fever and serositis. The level of awareness about familial Mediterranean fever is far from sufficient, and it is assumed that there may be many patients with this disease who are under observation without an accurate diagnosis. CASE PRESENTATION: A 30-year-old Japanese man presented to us with a few years’ history of recurrent episodes of fever, abdominal pain and diarrhea. He often visited a hospital when the attacks occurred; however, acute enteritis was diagnosed each time, and the symptoms resolved spontaneously within a few days. When he noticed a shortening of the interval between the attacks, he visited the hospital again. Upper endoscopy and colonoscopy performed at this hospital revealed no significant abnormal findings. He was then referred to our hospital under the suspicion of a small intestinal disease. Abdominal computed tomography revealed wall thickening and increased density of the mesenteric adipose tissue in the jejunum, which led us to suspect Crohn’s disease. Oral double-balloon enteroscopy was performed; because this revealed only mild mucosal edema in the jejunum, Crohn’s disease was considered to be highly improbable. Based on the patient’s clinical course, we suspected familial Mediterranean fever. As the Livneh criteria for familial Mediterranean fever were satisfied, the patient was started on oral colchicine for the purpose of diagnostic treatment. A definitive diagnosis of familial Mediterranean fever was then made based on the detection of a mutation of the Mediterranean fever gene. A marked reduction in the frequency of attacks was observed in response to colchicine treatment. CONCLUSIONS: Although Crohn’s disease may be considered first in the differential diagnosis of young patients presenting with periodic fever, abdominal pain and diarrhea, the possibility of familial Mediterranean fever should also be borne in mind. |
format | Online Article Text |
id | pubmed-4182779 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41827792014-10-03 Familial Mediterranean fever in which Crohn’s disease was suspected: a case report Matsumoto, Satohiro Urayoshi, Shunsuke Yoshida, Yukio BMC Res Notes Case Report BACKGROUND: Familial Mediterranean fever is a hereditary autoinflammatory disease, mainly characterized by periodic fever and serositis. The level of awareness about familial Mediterranean fever is far from sufficient, and it is assumed that there may be many patients with this disease who are under observation without an accurate diagnosis. CASE PRESENTATION: A 30-year-old Japanese man presented to us with a few years’ history of recurrent episodes of fever, abdominal pain and diarrhea. He often visited a hospital when the attacks occurred; however, acute enteritis was diagnosed each time, and the symptoms resolved spontaneously within a few days. When he noticed a shortening of the interval between the attacks, he visited the hospital again. Upper endoscopy and colonoscopy performed at this hospital revealed no significant abnormal findings. He was then referred to our hospital under the suspicion of a small intestinal disease. Abdominal computed tomography revealed wall thickening and increased density of the mesenteric adipose tissue in the jejunum, which led us to suspect Crohn’s disease. Oral double-balloon enteroscopy was performed; because this revealed only mild mucosal edema in the jejunum, Crohn’s disease was considered to be highly improbable. Based on the patient’s clinical course, we suspected familial Mediterranean fever. As the Livneh criteria for familial Mediterranean fever were satisfied, the patient was started on oral colchicine for the purpose of diagnostic treatment. A definitive diagnosis of familial Mediterranean fever was then made based on the detection of a mutation of the Mediterranean fever gene. A marked reduction in the frequency of attacks was observed in response to colchicine treatment. CONCLUSIONS: Although Crohn’s disease may be considered first in the differential diagnosis of young patients presenting with periodic fever, abdominal pain and diarrhea, the possibility of familial Mediterranean fever should also be borne in mind. BioMed Central 2014-09-27 /pmc/articles/PMC4182779/ /pubmed/25261084 http://dx.doi.org/10.1186/1756-0500-7-678 Text en © Matsumoto et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Matsumoto, Satohiro Urayoshi, Shunsuke Yoshida, Yukio Familial Mediterranean fever in which Crohn’s disease was suspected: a case report |
title | Familial Mediterranean fever in which Crohn’s disease was suspected: a case report |
title_full | Familial Mediterranean fever in which Crohn’s disease was suspected: a case report |
title_fullStr | Familial Mediterranean fever in which Crohn’s disease was suspected: a case report |
title_full_unstemmed | Familial Mediterranean fever in which Crohn’s disease was suspected: a case report |
title_short | Familial Mediterranean fever in which Crohn’s disease was suspected: a case report |
title_sort | familial mediterranean fever in which crohn’s disease was suspected: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4182779/ https://www.ncbi.nlm.nih.gov/pubmed/25261084 http://dx.doi.org/10.1186/1756-0500-7-678 |
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