RECURRENT EPISODES OF FEVER AND ARTHRITIS IN AN ADULT PATIENT
Author(s) -
Claudia Cobilinschi,
Daniela Opriş-Belinski,
Denisa Predețeanu,
Ruxandra Ionescu
Publication year - 2017
Publication title -
romanian journal of rheumatology
Language(s) - English
Resource type - Journals
eISSN - 2069-6086
pISSN - 1843-0791
DOI - 10.37897/rjr.2017.2.8
Subject(s) - familial mediterranean fever , mefv , medicine , colchicine , amyloidosis , arthritis , pyrin domain , complication , dermatology , gene mutation , mutation , gene , disease , genetics , inflammation , biology , inflammasome
Familial Mediterranean Fever (FMF) is the most common condition in the group of autoinflammatory diseases. It has a relatively heterogeneous clinical display included in the Tel-Hashomer diagnostic criteria that can be further confirmed by genetic testing showing a mutation in the MEFV gene. AA Amyloidosis is the most sever complication in these patients. Colchicine is the standard treatment and/or alternative biological agents if necessary. This article aims to describe the evolution of a patient with FMF, firstly diagnosed as reactive arthritis, his clinical manifestations and therapeutic options.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom