Familial Mediterranean fever and mesangial proliferative glomerulonephritis: Report of a case and review of the literature

Cagdas D. N. , Gucer S., Kale G., Duzova A. , Ozen S.

Pediatric Nephrology, cilt.20, sa.9, ss.1352-1354, 2005 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 20 Konu: 9
  • Basım Tarihi: 2005
  • Doi Numarası: 10.1007/s00467-005-1991-9
  • Dergi Adı: Pediatric Nephrology
  • Sayfa Sayıları: ss.1352-1354


In familial Mediterranean fever (FMF), a genetically inherited disease characterized by fever and serositis, renal involvement is mainly AA amyloidosis. We report a patient with FMF who developed mesangial proliferative glomerulonephritis; presumably in response to colchicine treatment, the activity of the disease decreased and renal function tests and urinary findings normalized. This report emphasizes the concurrent existence of mesangial proliferative glomerulonephritis with FMF in the absence of renal amyloidosis. Due to increased inflammatory response observed in FMF, immunologic glomerular injury, a common cause of glomerulonephritis, may occur more frequently in patients with FMF.