The Turkish Journal of Pediatrics 2018 , Vol 60 , Num 3
Polyarteritis nodosa in case of familial Mediterranean fever
İbrahim Gökçe 1 ,Ülger Altuntaş 1 ,Deniz Filinte 2 ,Harika Alpay 1
1 Division of Pediatric Nephrology, Department of Pediatrics, Marmara University Faculty of Medicine, İstanbul, Turkey
2 Department of Pathology, Marmara University Faculty of Medicine, İstanbul, Turkey
DOI : 10.24953/turkjped.2018.03.016 Gökçe İ, Altuntaş Ü, Filinte D, Alpay H. Polyarteritis nodosa in case of familial Mediterranean fever. Turk J Pediatr 2018; 60: 326-330.

Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by recurrent self-limited attacks of fever accompanied by peritonitis, pleuritis, and arthritis. Protracted febrile myalgia syndrome (PFMS) is a rare form of vasculitic disease which is an uncommon dramatic manifestation of FMF, characterized by severe crippling myalgia and high fever. Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis affecting medium or small arteries. It is rarely observed in children, but its incidence increases in the presence of FMF. In this article we described a 14-year-old child diagnosed with FMF associated with PAN. Physicians should be aware of this possible association. Keywords : familial Mediterranean fever, protracted febrile myalgia syndrome, polyarteritis nodosa

Copyright © 2016 turkishjournalpediatrics.org