Polyarteritis nodosa in case of familial Mediterranean fever

Amaç & Hipotez:Familial Mediterranean fever (FMF) is an autosomal recessive diseasecharacterized by recurrent self-limited attacks of fever accompanied byperitonitis, pleuritis, and arthritis.

📊

Temel Bulgular & Veri:It is rarely observed in children, but its incidenceincreases in the presence of FMF.

💡

Sonuç & Katkı:Physicians should be awareof this possible association.

🔬Tür:Araştırma Makalesi

📍Kapsam:Genişletilmiş Akademik Örneklem

⚙️Değişkenler:Alan Parametreleri

Özet

Familial Mediterranean fever (FMF) is an autosomal recessive diseasecharacterized by recurrent self-limited attacks of fever accompanied byperitonitis, pleuritis, and arthritis. Protracted febrile myalgia syndrome(PFMS) is a rare form of vasculitic disease which is an uncommon dramaticmanifestation of FMF, characterized by severe crippling myalgia and highfever. Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis affectingmedium or small arteries. It is rarely observed in children, but its incidenceincreases in the presence of FMF. In this article we described a 14-year-oldchild diagnosed with FMF associated with PAN. Physicians should be awareof this possible association.

🔖

Bu Makaleye Atıf Yap

GÖKCE, İ., ALTUNTAŞ, Ü., FİLİNTE, D., ALPAY, H. (2018). Polyarteritis nodosa in case of familial Mediterranean fever. Turkish Journal of Pediatrics, Cilt: 60 - Sayı: 3, 326–330. https://ajindex.com/articles/412117

📄 Tam Metin PDF Okuyucu

Yeni Sekmede Aç ↗

↗Yeni Sekme

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (14)

Soylu A, Kasap B, Türkmen M, Saylam GS, Kavukçu S. Febrile myalgia syndrome in familial Mediterranean fever. J Clin Rheumatol 2006; 12: 93-96
Bircan Z, Usluer H. Protracted febrile myalgia mimicking polyarteritis nodosa. J Clin Rheumatol 2008; 14: 222-225
Yalçinkaya F, Ozçakar ZB, Kasapçopur O, et al. Prevalence of the MEFV gene mutations in childhood polyarteritis nodosa. J Pediatr 2007; 151: 675-678
Ozen S, Pistorio A, Iusan SM, et al. EULAR/PRINTO/ PRES criteria for Henoch-Schonlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: Final classification criteria. Ann Rheum Dis 2010; 69: 798-806
Bakkaloğlu SA, Muzaç S, Akpek S, Söylemezoğlu O, Buyan N, Hasanoğlu E. Polyarteritis nodosa in a case of familial Mediterranean fever Pediatr Nephrol 2004; 19: 536-538
Yılmaz Ağladıoğlu S, Bakkaloğlu Ezgü S, Peru H ve ark. Ailevi Akdeniz ateşi ve poliarteritis nodoza birlikteliği olan pediatrik bir olgu sunumu. Gazi Tıp Dergisi 2008; 3: 144-146
Ozen S, Ben-Chetrit E, Bakkaloglu A, et al. Polyarteritis nodosa in patients with Familial Mediterranean Fever (FMF): a concomitant disease or a feature of FMF? Semin Arthritis Rheum 2001; 30: 281-287
Samuels J, Ozen S. Familial Mediterranean fever and the other autoinflammatory syndromes: evaluation of the patient with recurrent fever. Curr Opin Rheumatol 2006; 18: 108-117
Aksu K, Keser G. Coexistence of vasculitides with familial Mediterranean fever. Rheumatol Int 2011; 31: 1263-1274
Langevitz P, Zemer D, Livneh A, Shemer J, Pras M. Protracted febrile myalgia in patients with familial Mediterranean fever. J Rheumatol 1994; 21: 1708-1709
Majeed HA, Al-Qudah AK, Qubain H, Shahin HM. The clinical patterns of myalgia in children with familial Mediterranean fever. Semin Arthritis Rheum 2000; 30: 138-143
Kaplan E, Mukamel M, Barash J, et al. Protracted febrile myalgia in children and young adults with familial Mediterranean fever: analysis of 15 patients and suggested criteria for working diagnosis. Clin Exp Rheumatol 2007; 25(4 Suppl 45): 114-117
Gökce İ, Demirkaya E, Gök F. Protracted Febrile Myalgia in a child as the presenting sign of familial Mediterranean fever: case report and review of the literature. Balkan Med J 2011; 28: 222-223
Ozturk C, Halicioglu O, Coker I, et al. Association of clinical and genetical features in FMF with focus on MEFV strip assay sensitivity in 452 children