Home > Journals > Giornale Italiano di Dermatologia e Venereologia > Past Issues > Giornale Italiano di Dermatologia e Venereologia 2006 April;141(2) > Giornale Italiano di Dermatologia e Venereologia 2006 April;141(2):169-71

CURRENT ISSUE
 

ARTICLE TOOLS

Reprints

GIORNALE ITALIANO DI DERMATOLOGIA E VENEREOLOGIA

A Journal on Dermatology and Sexually Transmitted Diseases


Official Journal of the Italian Society of Dermatology and Sexually Transmitted Diseases
Indexed/Abstracted in: EMBASE, PubMed/MEDLINE, Science Citation Index Expanded (SciSearch), Scopus
Impact Factor 1,014


eTOC

 

CLINICAL CASES  


Giornale Italiano di Dermatologia e Venereologia 2006 April;141(2):169-71

language: English

Familial mediterranean fever. A diagnostic challenge

Mourellou O., Delli F. S., Chaidemenos G., Gidarokosta P., Tsatilas D., Tsatsou F.

State Hospital for Skin and Venereal Diseases Thessaloniki, Greece


PDF  


Familial Mediterranean fever (FMF) is a hereditary disease that especially affects people living around the Mediterranean sea. The most serious complication is amyloidosis, which can lead to terminal renal failure. We report the case of a 48-year old man who presented in our clinic with recurrent episodes of erysipelas-like rashes located at the right gluteal area, always associated with fever and sometimes with orchiepidedymitis, abdominal pain and arthritis. The clinical diagnosis of FMF was confirmed by the finding of the mutated marenostrin-encoding fever (MEFV) gene, using the PCR technique. The attacks were successfully avoided by continuous administration of colchicine per os 0.5 mg 3 times daily

top of page

Publication History

Cite this article as

Corresponding author e-mail