Familial Mediterranean Fever and Glomerulonrphritis: A Case Report

Year 2012, Volume: 13 Issue: 3, 25 - 26, 01.12.2012

Orhan Zengin İbrahim Halil Türkbeyler Taner Babacan Yavuz Pehlivan Ahmet Mesut Onat

Abstract

Familial mediterranean fever is characterized by recurrent attacks of fever and polyserositis. Familial mediterranean fever is an autosomal recessive disease. Familial mediterranean fever is commonly seen in Jewish, Arab, Turkish and Armenian. The most important and prognosis-determining complication is kidney involvement. The most common cause of kidney involvement is AA type amyloidosis. Effective ad common use of colchicine decreased amyloidosis frequency when compared to before. It has been reported that frequency of amyloidosis in patients who don't use colchicine is around 20-25% in our country. During the course of familial mediterranean fever, renal pathologies such as glomerulonephritis can be seen other than amyloidosis. Here we present a patient with familial mediterranean fever and membranoproliferative glomerulonephritis.

Keywords

Familial Mediterranean fever, kidney involvement, glomerulonephritis

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• Dr. Ýbrahim Halil TÜRKBEYLER
• Gaziantep Üniversitesi Týp Fakültesi, Ýç Hastalýklarý AD, GAZÝANTEP, TÜRKÝYE 6,7 E-Posta
• : [e-mail] 8 Geliþ Tarihi
• Kabul Tarihi : 27.11.2011 9-11 26