Familial Mediterranean fever

Familial Mediterranean fever (FMF) is an autoinflammatory disorder characterized by recurrent short episodes of fever and serositis resulting in pain in the abdomen, chest, joints and muscles.

Peritonitis

Inflammation of the peritoneum.


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PMID (PMCID)
30511549
 MALE
Polyarteritis nodosa in case of familial Mediterranean fever.
Gokce , Altuntas U, Filinte D, Alpay H.
Turk J Pediatr. 2018;60(3):326-330.
Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by recurrent self-limited attacks of fever accompanied by peritonitis, pleuritis, and arthritis.
29624229
 MALE
Two cases of periodic fever syndrome with coexistent mevalonate kinase and Mediterranean fever gene mutations.
Cakan M, Aktay-Ayaz N, Keskindemirci G, Karadag G.
Turk J Pediatr. 2017;59(4):467-470.
Familial Mediterranean fever is the most common periodic fever syndrome and characterized by recurrent attacks of fever, arthritis, peritonitis, pleuritis that typically last 1-3 days.
29900978
 OTHER
Coexistence of Familial Mediterranean Fever With Ankylosing Spondylitis and Sjogren's Syndrome: A Rare Occurrence.
Dortbas F, Garip Y, Guler T, Karci AA.
Arch Rheumatol. 2016;31(1):87-90.
Familial Mediterranean fever is an autosomal recessive disease characterized by recurrent episodes of fever, peritonitis, synovitis, pleuritis, and erysipelas-like skin lesions.
26907752
(4767334)
 FEMALE Adult
Episode of Familial Mediterranean Fever-Related Peritonitis in the Second Trimester of Pregnancy Followed by Acute Cholecystitis: Dilemmas and Pitfalls.
Kosmidis C, Anthimidis G, Varsamis N, Makedou F, Georgakoudi E, Efthimiadis C.
Am J Case Rep. 2016;17:115-9.
Episode of Familial Mediterranean Fever-Related Peritonitis in the Second Trimester of Pregnancy Followed by Acute Cholecystitis: Dilemmas and Pitfalls.
26907752
(4767334)
 FEMALE Adult
Episode of Familial Mediterranean Fever-Related Peritonitis in the Second Trimester of Pregnancy Followed by Acute Cholecystitis: Dilemmas and Pitfalls.
Kosmidis C, Anthimidis G, Varsamis N, Makedou F, Georgakoudi E, Efthimiadis C.
Am J Case Rep. 2016;17:115-9.
Occurrence of Familial Mediterranean Fever (FMF) paroxysm of peritonitis and acute cholecystitis during pregnancy is a unique clinical entity that leads to serious diagnostic and therapeutic dilemmas.
24533546
 FEMALE
Coexistence of two rare genetic disorders: Kartagener syndrome and familial Mediterranean fever.
Cetin D, Genc Cetin B, enturk T, ahin Cildag S, Ylmaz Akdam .
Mod Rheumatol. 2015;25(2):312-4.
Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by recurrent attacks of fever and peritonitis, pleuritis, arthritis, or erysipelas-like skin disease.
25398289
 FEMALE Adult
Intrauterine device may trigger typical attacks of familial Mediterranean fever: a case report.
Kurultak I, Kinalp C, Ceri M, Evrenkaya TR.
Wien Klin Wochenschr. 2015;127(1-2):68-70.
Familial Mediterranean fever (FMF) is an autosomal recessive disorder characterized by episodic, recurrent, self-limited attacks of fever and serositis (sterile peritonitis, pleuritis, arthritis, etc).
27604438
 MALE
Patient with Recurrent Polyserositis (Familial Mediterranean Fever).
Agarwal A, Sharma S.
J Assoc Physicians India. 2015;63(8):71-4.
The disorder has been given various names including familial paroxysmal polyserositis, periodic peritonitis, recurrent polyserositis, benign paroxysmal peritonitis, and periodic disease or periodic fever, As the name indicates, FMF occurs within families and is much more common in individuals of Mediterranean descent than in persons of any other ethnicity.
27604438
 MALE
Patient with Recurrent Polyserositis (Familial Mediterranean Fever).
Agarwal A, Sharma S.
J Assoc Physicians India. 2015;63(8):71-4.
The disorder has been given various names including familial paroxysmal polyserositis, periodic peritonitis, recurrent polyserositis, benign paroxysmal peritonitis, and periodic disease or periodic fever, As the name indicates, FMF occurs within families and is much more common in individuals of Mediterranean descent than in persons of any other ethnicity.
27604438
 MALE
Patient with Recurrent Polyserositis (Familial Mediterranean Fever).
Agarwal A, Sharma S.
J Assoc Physicians India. 2015;63(8):71-4.
The disorder has been given various names including familial paroxysmal polyserositis, periodic peritonitis, recurrent polyserositis, benign paroxysmal peritonitis, and periodic disease or periodic fever, As the name indicates, FMF occurs within families and is much more common in individuals of Mediterranean descent than in persons of any other ethnicity.
25109905
 MALE Adult
Cutaneous necrotizing vasculitis as a manifestation of familial Mediterranean fever.
Komatsu S, Honma M, Igawa S, Tsuji H, Ishida-Yamamoto A, Migita K, Ida H, Iizuka H.
J Dermatol. 2014;41(9):827-9.
Familial Mediterranean Fever (FMF) is a hereditary autoinflammatory disease, which is characterized by recurrent and paroxysmal fever, peritonitis, arthritis, myalgia, and skin rashes.
23400211
(3565148)
 MALE Young Adult
Extensive thrombosis in a patient with familial Mediterranean fever, despite hyperimmunoglobulin D state in serum. [corrected].
Joo K, Park W, Chung MH, Lim MJ, Jung KH, Heo Y, Kwon SR.
J Korean Med Sci. 2013;28(2):328-30.
Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by recurrent episodes of fever accompanied by peritonitis, pleuritis, arthritis, or erysipelas-like erythema.
24383976
 MIXED_SAMPLE Adult
Three Japanese patients (mother and two children) with familial Mediterranean fever associated with compound heterozygosity for L110P/E148Q/M694I and an autosomal true dominant inheritance pattern.
Fukushima Y, Obara K, Hirata H, Sugiyama K, Fukuda T, Takabe K.
Asian Pac J Allergy Immunol. 2013;31(4):325-9.
Familial Mediterranean fever (FMF) is characterized by repeated episodes of fever, peritonitis, pleuritis, and synovitis.
23453719
 MALE
[Cutaneous polymorph manifestations of familial Mediterranean fever in a child].
Gonzales F, Begon Lours J, Kalach N, Gosset P, Lasek Duriez A.
Arch Pediatr. 2013;20(4):382-5.
Familial Mediterranean fever is an autosomal recessive disorder characterized by recurrent attacks of fever and polyserositis including peritonitis, pleuritis, and arthritis.
22675839
 MALE Adult
"Trap" the diagnosis: a man with recurrent episodes of febrile peritonitis, not just familial Mediterranean fever.
Arad U, Niv E, Caspi D, Elkayam O.
Isr Med Assoc J. 2012;14(4):229-31.
"Trap" the diagnosis: a man with recurrent episodes of febrile peritonitis, not just familial Mediterranean fever.
21416236
 MALE Young Adult
Coexistence of Takayasu's arteritis with familial Mediterranean fever.
Zihni FY, Kalfa M, Ocakc PT, Tarhan F, Parildar M, Keser G, Aksu K.
Rheumatol Int. 2012;32(6):1675-8.
Familial Mediterranean fever (FMF) is the most common autoinflammatory disease characterized by recurrent self-limited attacks of fever, accompanied with peritonitis, pleuritis or arthritis.
21259007
 FEMALE Child
Polyarteritis nodosa and Henoch-Schonlein purpura nephritis in a child with familial Mediterranean fever: a case report.
Girisgen I, Sonmez F, Koseoglu K, Erisen S, Yilmaz D.
Rheumatol Int. 2012;32(2):529-33.
Familial Mediterranean fever is an autosomal recessive disease characterized by recurrent self-limited attacks of fever accompanied by peritonitis, pleuritis, and arthritis.
21567247
 MIXED_SAMPLE Adult
Anti-TNF agents in familial Mediterranean fever: report of three cases and review of the literature.
Ozgocmen S, Akgul O.
Mod Rheumatol. 2011;21(6):684-90.
Familial Mediterranean fever (FMF) is an autoinflammatory disease characterized by recurrent fever, peritonitis/pleuritis, or arthritis attacks.
21483284
 FEMALE Child
[Protracted Febrile Myalgia Syndrome with Henoch-Schonlein Purpura: an atypical presentation of Familial Mediterranean Fever].
Cabral M, Conde M, Brito MJ, Almeida H, Melo Gomes JA.
Acta Reumatol Port. 2011;36(1):69-74.
Familial Mediterranean Fever (FMF) is an hereditary autosomal recessive disease characterized by recurrent attacks of fever, arthritis and serositis: peritonitis, pleurisy and/or pericarditis.
20962446
 FEMALE Adult
Periodic peritonitis due to familial Mediterranean fever in a patient with systemic lupus erythematosus.
Matsuda M, Kishida D, Tsuchiya-Suzuki A, Fukushima K, Shimojima Y, Yazaki M, Ikeda S.
Intern Med. 2010;49(20):2259-62.
Periodic peritonitis due to familial Mediterranean fever in a patient with systemic lupus erythematosus.