Yıl: 2017 Cilt: 63 Sayı: 2 Sayfa Aralığı: 174 - 177 Metin Dili: İngilizce İndeks Tarihi: 29-07-2022

Coexistence of familial Mediterranean fever and Behçet’s disease: a case report

Öz:
Behçet’s disease (BD) is a chronic, multi-systemic vasculitis, characterized by a triad of recurrent aphthous stomatitis, genital aphthae, and uveitis. It is common in the Eastern Mediterranean, Middle East, and Eastern Asian countries. Familial Mediterranean fever (FMF) is an autosomal recessive autoinflammatory disorder, which is common seen in the Turkish, Armenian, Arabic, and Sephardic Jewish populations. It is characterized by recurrent episodes of fever, peritonitis, pleuritis, arthritis, and erysipelas-like skin lesions. Behçet’s disease and FMF have common clinical features and geographic distribution. Herein, we present a 19-year-old female patient with coexistence of FMF and BD in the light of literature data
Anahtar Kelime:

Konular: Rehabilitasyon
Belge Türü: Makale Makale Türü: Olgu Sunumu Erişim Türü: Erişime Açık
  • 1. Yazici A, Cefle A, Savli H. The frequency of MEFV gene mutations in Behcet’s disease and their relation with clinical findings. Rheumatol Int 2012;32:3025-30.
  • 2. Srivastava N, Chand S, Bansal M, Srivastava K, Singh S. Familial Behcet’s disease. Indian J Dermatol Venereol Leprol 2007;73:260-1.
  • 3. Yokota K, Fukuda M, Migita K, Tanaka E, Okamoto T, Kimura K. Three patients with familial Mediterranean fever: a possible underdiagnosed entity in Japan. Intern Med 2014;53:2013-6.
  • 4. Cazeneuve C, Hovannesyan Z, Geneviève D, Hayrapetyan H, Papin S, Girodon-Boulandet E, et al. Familial Mediterranean fever among patients from Karabakh and the diagnostic value of MEFV gene analysis in all classically affected populations. Arthritis Rheum 2003;48:2324-31.
  • 5. Berkun Y, Eisenstein EM. Diagnostic criteria of familial Mediterranean fever. Autoimmun Rev 2014;13:388-90.
  • 6. Touitou I, Magne X, Molinari N, Navarro A, Quellec AL, Picco P, et al. MEFV mutations in Behçet’s disease. Hum Mutat 2000;16:271-2.
  • 7. Imirzalioglu N, Dursun A, Tastan B, Soysal Y, Yakicier MC. MEFV gene is a probable susceptibility gene for Behçet’s disease. Scand J Rheumatol 2005;34:56-8.
  • 8. Esmaeili M, Bonyadi M, Khabbazi A, Ebrahimi AA, Sharif SK, Hajialilo M, et al. Common MEFV mutations in Iranian Azeri Turkish patients with Behçet’s disease. Scand J Rheumatol 2011;40:383-6.
  • 9. Ayesh S, Abu-Rmaileh H, Nassar S, Al-Shareef W, Abu-Libdeh B, Muhanna A, et al. Molecular analysis of MEFV gene mutations among Palestinian patients with Behcet’s disease. Scand J Rheumatol 2008;37:370-4.
  • 10. Livneh A, Langevitz P, Zemer D, Zaks N, Kees S, Lidar T, et al. Criteria for the diagnosis of familial Mediterranean fever. Arthritis Rheum 1997;40:1879-85.
  • 11. Saleh Z, Arayssi T. Update on the therapy of Behçet disease. Ther Adv Chronic Dis 2014;5:112-34.
  • 12. Melikoglu M, Melikoglu MA. The prevalence of fibromyalgia in patients with Behçet’s disease and its relation with disease activity. Rheumatol Int 2013;33:1219-22.
  • 13. Melikoglu M, Melikoglu MA. The prevalence of fibromyalgia in patients with Behçet’s disease and its relation with disease activity. Rheumatol Int 2013;33:1219-22.
  • 14. Kaşifoğlu T, Calişir C, Cansu DU, Korkmaz C. The frequency of sacroiliitis in familial Mediterranean fever and the role of HLA-B27 and MEFV mutations in the development of sacroiliitis. Clin Rheumatol 2009;28:41-6.
  • 15. Criteria for diagnosis of Behçet’s disease. International Study Group for Behçet’s Disease. Lancet 1990;335:1078-80.
  • 16. Matsuda M, Nakamura A, Tsuchiya S, Yoshida T, Horie S, Ikeda S. Coexistence of familial Mediterranean fever and Behçet’s disease in a Japanese patient. Intern Med 2006;45:799-800.
  • 17. Birlik M, Tunca M, Hizli N, Soytürk M, Yeniçerioğlu Y, Ozcan MA, et al. Coexistence of familial Mediterranean fever with sacroiliitis and Behçet’s disease: a rare occurrence. Clin Rheumatol 1998;17:397-9.
  • 18. Mobini M. Familial mediterranean fever in an Iranian patient with behcet disease. Caspian J Intern Med 2011;2:344-6.
  • 19. Rabinovich E, Shinar Y, Leiba M, Ehrenfeld M, Langevitz P, Livneh A. Common FMF alleles may predispose to development of Behcet’s disease with increased risk for venous thrombosis. Scand J Rheumatol 2007;36:48-52.
  • 20. Tasliyurt T, Yigit S, Rustemoglu A, Gul U, Ates O. Common MEFV gene mutations in Turkish patients with Behcet’s disease. Gene 2013;530:100-3.
  • 21. Schwartz T, Langevitz P, Zemer D, Gazit E, Pras M, Livneh A. Behçet’s disease in Familial Mediterranean fever: characterization of the association between the two diseases. Semin Arthritis Rheum 2000;29:286-95.
  • 22. Espinosa G, Arostegui JI, Plaza S, Rius J, Cervera R, Yagüe J, et al. Behçet’s disease and hereditary periodic fever syndromes: casual association or causal relationship? Clin Exp Rheumatol 2005;23:64-6.
  • 23. Ben-Chetrit E, Cohen R, Chajek-Shaul T. Familial mediterranean fever and Behçet’s disease--are they associated? J Rheumatol 2002;29:530-4.
  • 24. Aksu K, Keser G. Coexistence of vasculitides with familial Mediterranean fever. Rheumatol Int 2011;31:1263-74.
APA Güler T, garip y, DÖRTBAŞ F, KARCI A, ÇİFCİ ASLAN N (2017). Coexistence of familial Mediterranean fever and Behçet’s disease: a case report. , 174 - 177.
Chicago Güler Tuba,garip yesim,DÖRTBAŞ Fulya,KARCI Ayşe Aslıhan,ÇİFCİ ASLAN NURŞAD Coexistence of familial Mediterranean fever and Behçet’s disease: a case report. (2017): 174 - 177.
MLA Güler Tuba,garip yesim,DÖRTBAŞ Fulya,KARCI Ayşe Aslıhan,ÇİFCİ ASLAN NURŞAD Coexistence of familial Mediterranean fever and Behçet’s disease: a case report. , 2017, ss.174 - 177.
AMA Güler T,garip y,DÖRTBAŞ F,KARCI A,ÇİFCİ ASLAN N Coexistence of familial Mediterranean fever and Behçet’s disease: a case report. . 2017; 174 - 177.
Vancouver Güler T,garip y,DÖRTBAŞ F,KARCI A,ÇİFCİ ASLAN N Coexistence of familial Mediterranean fever and Behçet’s disease: a case report. . 2017; 174 - 177.
IEEE Güler T,garip y,DÖRTBAŞ F,KARCI A,ÇİFCİ ASLAN N "Coexistence of familial Mediterranean fever and Behçet’s disease: a case report." , ss.174 - 177, 2017.
ISNAD Güler, Tuba vd. "Coexistence of familial Mediterranean fever and Behçet’s disease: a case report". (2017), 174-177.
APA Güler T, garip y, DÖRTBAŞ F, KARCI A, ÇİFCİ ASLAN N (2017). Coexistence of familial Mediterranean fever and Behçet’s disease: a case report. Türkiye Fiziksel Tıp ve Rehabilitasyon Dergisi, 63(2), 174 - 177.
Chicago Güler Tuba,garip yesim,DÖRTBAŞ Fulya,KARCI Ayşe Aslıhan,ÇİFCİ ASLAN NURŞAD Coexistence of familial Mediterranean fever and Behçet’s disease: a case report. Türkiye Fiziksel Tıp ve Rehabilitasyon Dergisi 63, no.2 (2017): 174 - 177.
MLA Güler Tuba,garip yesim,DÖRTBAŞ Fulya,KARCI Ayşe Aslıhan,ÇİFCİ ASLAN NURŞAD Coexistence of familial Mediterranean fever and Behçet’s disease: a case report. Türkiye Fiziksel Tıp ve Rehabilitasyon Dergisi, vol.63, no.2, 2017, ss.174 - 177.
AMA Güler T,garip y,DÖRTBAŞ F,KARCI A,ÇİFCİ ASLAN N Coexistence of familial Mediterranean fever and Behçet’s disease: a case report. Türkiye Fiziksel Tıp ve Rehabilitasyon Dergisi. 2017; 63(2): 174 - 177.
Vancouver Güler T,garip y,DÖRTBAŞ F,KARCI A,ÇİFCİ ASLAN N Coexistence of familial Mediterranean fever and Behçet’s disease: a case report. Türkiye Fiziksel Tıp ve Rehabilitasyon Dergisi. 2017; 63(2): 174 - 177.
IEEE Güler T,garip y,DÖRTBAŞ F,KARCI A,ÇİFCİ ASLAN N "Coexistence of familial Mediterranean fever and Behçet’s disease: a case report." Türkiye Fiziksel Tıp ve Rehabilitasyon Dergisi, 63, ss.174 - 177, 2017.
ISNAD Güler, Tuba vd. "Coexistence of familial Mediterranean fever and Behçet’s disease: a case report". Türkiye Fiziksel Tıp ve Rehabilitasyon Dergisi 63/2 (2017), 174-177.