Relationship Between Familial Mediterranean Fever and Other Rheumatic Diseases: Coincidence or Coexistence?

نویسندگان

چکیده

Background: Familial Mediterranean fever (FMF) is the most common monogenic autoinflammatory disease affecting mainly ethnic groups of basin. It has been reported that it can coexist with various systemic inflammatory diseases. This study aimed to obtain information on rheumatic diseases accompany FMF and evaluate relation between such diseases.
 Methods: Eighty-four patients diagnosed have comorbidity in rheumatology clinic January 2018 - March 2020 were included this study. 
 Results: The accompanying was spondyloarthritis 36 patients. Vasculitides second 22, followed by connective tissue 13, rheumatoid arthritis 5, juvenile idiopathic 4, gout 3, hidradenitis suppurativa 1 MEFV mutation observed M694V. There no significant difference demographic characteristics clinical manifestations M694V types. Conclusions: In study, determined. Two new conditions, eosinophilic granulomatous polyangiitis, scleroderma detected. associations may be just coincidental or an extension underlying pathology. To aware association important early diagnosis appropriate treatment.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Pulmonary hypertension in familial Mediterranean fever: consequence or coincidence?

Objectives FMF is the most common autoinflammatory disease characterized by recurrent febrile polyserositis. The gravest consequence of FMF is nephropatic amyloidosis of AA type, which may progress to affect other organs, including the lungs[]. Pulmonary hypertension (PH) in FMF related amyloidosis is rare; only a few cases have been reported so far[,]. We aim to elucidate development of PH in ...

متن کامل

Coexistence of sarcoidosis and Familial Mediterranean Fever.

Sarcoidosis is a chronic inflammatory disease with unknown cause characterized by non-caseating granuloma formations. It may present with bilateral hilar lymphadenopathy, skin lesions, the involvement of eye and symptoms on the locomotor system. FMF (Familial Mediterranean Fever) is an autosomal recessive autoinflammatory disease, characterized by recurrent episodes of fever and polyserositis. ...

متن کامل

Relationship between endothelial dysfunction and microalbuminuria in familial Mediterranean fever.

OBJECTIVE The aim of our study is to investigate the relationship between microalbuminuria and flow-mediated dilatation in familial Mediterranean fever (FMF) patients. MATERIAL AND METHODS In our study, there were two groups consisting of 54 patients who were out of the attack period (43 of whom had no microalbuminuria and 11 of whom had microalbuminuria) and 40 healthy controls (M/F: 12/28)....

متن کامل

Familial Mediterranean Fever and Human autoinflammatory diseases

Introduction Human Autoinflammatory Diseases (HADs) is a heterogeneous group of rare genetic diseases, which are characterized by unprovoked onsets of inflammation, fever and clinical symptoms analogous with rheumatic diseases with absence of immunological indicators. Familial Mediterranean Diseases (FMF) is one of the popular forms in the group of syndromes which are called HPFS. Clinical char...

متن کامل

Coexistence of familial Mediterranean fever and rheumatoid arthritis.

Familial Mediterranean fever (FMF) is an autoinflammatory disorder characterized by recurrent febrile polyserositis and arthritis. Although accompanying seronegative spondyloarthropathy has been reported in FMF, coexistence with rheumatoid arthritis (RA) is very rare. This case report describes a Japanese female RA patient who presented with periodic fever. Genetic analysis revealed compound he...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Turkish journal of internal medicine

سال: 2022

ISSN: ['2687-4245']

DOI: https://doi.org/10.46310/tjim.982632