Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean Fever

Familial Mediterranean fever (FMF) is an autoinflammatory disorder with autosomal recessive inheritance, characterized by recurrent fever and episodes of serositis. The condition is known to be caused by mutations in the MEFV (Mediterranean FeVer) gene, located in the short arm of chromosome 16. Whi...

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Main Authors: Yunus Ugan, Atalay Doğru, Hüseyin Şencan, Mehmet Şahin, Şevket Ercan Tunç
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Case Reports in Medicine
Online Access:http://dx.doi.org/10.1155/2016/5134546
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author Yunus Ugan
Atalay Doğru
Hüseyin Şencan
Mehmet Şahin
Şevket Ercan Tunç
author_facet Yunus Ugan
Atalay Doğru
Hüseyin Şencan
Mehmet Şahin
Şevket Ercan Tunç
author_sort Yunus Ugan
collection DOAJ
description Familial Mediterranean fever (FMF) is an autoinflammatory disorder with autosomal recessive inheritance, characterized by recurrent fever and episodes of serositis. The condition is known to be caused by mutations in the MEFV (Mediterranean FeVer) gene, located in the short arm of chromosome 16. While more than 310 sequence variants in the MEFV gene have been described to date, the diagnosis is still established clinically. FMF may be accompanied by sacroiliitis and various forms of vasculitis. The most common forms of associated vasculitis are Henoch-Schonlein purpura and polyarteritis nodosa (PAN). We have presented here a fairly rare case of FMF, accompanied by both sacroiliitis and PAN.
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institution Kabale University
issn 1687-9627
1687-9635
language English
publishDate 2016-01-01
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series Case Reports in Medicine
spelling doaj-art-32c1407a67484b85b2af7469d7bca2a42025-02-03T06:01:35ZengWileyCase Reports in Medicine1687-96271687-96352016-01-01201610.1155/2016/51345465134546Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean FeverYunus Ugan0Atalay Doğru1Hüseyin Şencan2Mehmet Şahin3Şevket Ercan Tunç4Faculty of Medicine, Department of Internal Medicine, Division of Rheumatology, Suleyman Demirel University, 32260 Isparta, TurkeyFaculty of Medicine, Department of Internal Medicine, Division of Rheumatology, Suleyman Demirel University, 32260 Isparta, TurkeyFaculty of Medicine, Department of Internal Medicine, Suleyman Demirel University, 32260 Isparta, TurkeyFaculty of Medicine, Department of Internal Medicine, Division of Rheumatology, Suleyman Demirel University, 32260 Isparta, TurkeyFaculty of Medicine, Department of Internal Medicine, Division of Rheumatology, Suleyman Demirel University, 32260 Isparta, TurkeyFamilial Mediterranean fever (FMF) is an autoinflammatory disorder with autosomal recessive inheritance, characterized by recurrent fever and episodes of serositis. The condition is known to be caused by mutations in the MEFV (Mediterranean FeVer) gene, located in the short arm of chromosome 16. While more than 310 sequence variants in the MEFV gene have been described to date, the diagnosis is still established clinically. FMF may be accompanied by sacroiliitis and various forms of vasculitis. The most common forms of associated vasculitis are Henoch-Schonlein purpura and polyarteritis nodosa (PAN). We have presented here a fairly rare case of FMF, accompanied by both sacroiliitis and PAN.http://dx.doi.org/10.1155/2016/5134546
spellingShingle Yunus Ugan
Atalay Doğru
Hüseyin Şencan
Mehmet Şahin
Şevket Ercan Tunç
Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean Fever
Case Reports in Medicine
title Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean Fever
title_full Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean Fever
title_fullStr Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean Fever
title_full_unstemmed Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean Fever
title_short Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean Fever
title_sort sacroiliitis and polyarteritis nodosa in a patient with familial mediterranean fever
url http://dx.doi.org/10.1155/2016/5134546
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