Coexistence of polymyositis and familial Mediterranean fever

被引：4

作者：

Eguchi, Mami ^{[1
]}

Miyashita, Taiichiro ^{[1
]}

Shirouzu, Haruka ^{[1
]}

Sato, Saya ^{[1
]}

Izumi, Yasumori ^{[1
]}

Takeoka, Atsushi ^{[1
]}

Ohno, Tadayoshi ^{[1
]}

Sumiyoshi, Remi ^{[1
]}

Nishino, Ayako ^{[1
]}

Jiuchi, Yuka ^{[1
]}

Nonaka, Fumiaki ^{[2
]}

Eguchi, Katsumi ^{[2
]}

Kawakami, Atsushi ^{[3
]}

Migita, Kiyoshi ^{[1
]}

机构：

[1] NHO Natl Nagasaki Med Ctr, Clin Res Ctr, Dept Gen Internal Med & Rheumatol, Omura 8568652, Japan

[2] Sasebo City Gen Hosp, Dept Rheumatol, Sasebo, Japan

[3] Nagasaki Univ Hosp, Dept Rheumatol, Nagasaki, Japan

来源：

MODERN RHEUMATOLOGY | 2013年 / 23卷 / 02期

关键词：

Familial Mediterranean fever; CD64; MEFV gene; Polymyositis; PROTRACTED FEBRILE MYALGIA; DISEASE-CAUSING MUTATION; MEFV GENE; CRITERIA; DERMATOMYOSITIS; EXPRESSION; DIAGNOSIS; SPECTRUM; CHILDREN; CD64;

D O I：

10.1007/s10165-012-0649-2

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Familial Mediterranean fever (FMF) is an autosomal recessive disease affecting populations surrounding the Mediterranean area. In this case report, we report a Japanese female patient with polymyositis (PM) who presented with periodic fever. Genetic analysis revealed that she had compound heterozygous mutations in exon 2 of the MEFV gene (L110P/E148Q/R202Q). Treatment with colchicines (1.0 mg/day) successfully eliminated febrile attack and normalized the elevated levels of neutrophil CD64 expression, leading to the diagnosis of FMF. The association of FMF and PM has not previously been reported, so we discuss this rare association.

引用

页码：374 / 378

页数：5

共 50 条

[31] Coexistence of Systemic Lupus Erythematosus and Familial Mediterranean Fever
Yildiz, Guersel
Kayatas, Mansur
Uygun, Yasemin
Timucin, Meryem
Candan, Ferhan
INTERNAL MEDICINE, 2010, 49 (08) : 767 - 769
[32] Polyarteritis nodosa in case of familial Mediterranean fever
Gokce, Ibrahim
Altuntas, Ulger
Filinte, Deniz
Alpay, Harika
TURKISH JOURNAL OF PEDIATRICS, 2018, 60 (03) : 326 - 330
[33] Predictors of AA amyloidosis in familial Mediterranean fever
Mukhin, Nikolay A.
Kozlovskaya, Lidiya V.
Bogdanova, Marina V.
Rameev, Vilen V.
Moiseev, Sergey V.
Simonyan, Armine Kh.
RHEUMATOLOGY INTERNATIONAL, 2015, 35 (07) : 1257 - 1261
[34] Fingolimod in Multiple Sclerosis and Familial Mediterranean Fever Coexistence
Diker, Sevda
NEUROLOGY INDIA, 2022, 70 (01) : 392 - 394
[35] Coexistence of Takayasu’s arteritis with familial Mediterranean fever
Figen Yargucu Zihni
Melike Kalfa
Pınar Talu Ocakçı
Figen Tarhan
Mustafa Parildar
Gokhan Keser
Kenan Aksu
Rheumatology International, 2012, 32 : 1675 - 1678
[36] Screening of common and novel familial mediterranean fever mutations in south-east part of Turkey
Oztuzcu, Serdar
Ulasli, Mustafa
Ergun, Sercan
Igci, Yusuf Ziya
Igci, Mehri
Bayraktar, Recep
Nacarkahya, Gulper
Tamer, Ali
Cevik, Muammer Ozgur
Cakmak, Ecir Ali
Arslan, Ahmet
MOLECULAR BIOLOGY REPORTS, 2014, 41 (04) : 2601 - 2607
[37] Familial Mediterranean Fever in Siblings
Ozcakar, Z. Birsin
Erdogan, Beyza Doganay
Elhan, Atilla H.
Yalcinkaya, Fatos
JOURNAL OF RHEUMATOLOGY, 2012, 39 (11) : 2170 - 2174
[38] Protracted febrile myalgia as a first and challenging manifestation of familial Mediterranean fever
Aydin, Elif Arslanoglu
Baglan, Esra
Bagrul, Ilknur
Tuncez, Serife
Ozdel, Semanur
Bulbul, Mehmet
MODERN RHEUMATOLOGY, 2023, 33 (05) : 1030 - 1035
[39] Coexistence of hereditary angioedema in a case of familial Mediterranean fever with partial response to colchicine
Bahceci, Semiha Erdem
Genel, Ferah
Gulez, Nesrin
Nacaroglu, Hikmet T.
Central European Journal of Immunology, 2015, 40 (01) : 115 - 116
[40] Coexistence of Mixed Connective Tissue Disease and Familial Mediterranean Fever in a Japanese Patient
Fujita, Yuya
Asano, Tomoyuki
Sato, Shuzo
Furuya, Makiko Yashiro
Temmoku, Jumpei
Matsuoka, Naoki
Kobayashi, Hiroko
Watanabe, Hiroshi
Suzuki, Eiji
Koga, Tomohiro
Endo, Yushiro
Kawakami, Atsushi
Migita, Kiyoshi
INTERNAL MEDICINE, 2019, 58 (15) : 2235 - 2240

← 1 2 3 4 5 →