Familial Mediterranean fever and glomerulonephritis and review of the literature

被引：29

作者：

Akpolat, T ^{[1
]}

Akpolat, I

Karagoz, F

Yilmaz, E

Kandemir, B

Ozen, S

机构：

[1] Ondokuz Mayis Univ, Sch Med, Nefrol Bilim Dali, TR-55139 Samsun, Turkey

[2] Univ Hacettepe, Sch Med, TR-06100 Ankara, Turkey

来源：

RHEUMATOLOGY INTERNATIONAL | 2004年 / 24卷 / 01期

关键词：

colchicine; familial Mediterranean fever; glomerulonephritis; prednisolone;

D O I：

10.1007/s00296-003-0329-9

中图分类号：

R5 [内科学];

学科分类号：

1002 [临床医学]; 100201 [内科学];

摘要：

Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by recurrent and self-limited attacks of fever usually accompanied by polyserositis. Amyloidosis is its most common renal complication. A number of reports have shown vasculitic diseases such as polyarteritis nodosa and Henoch-Schonlein purpura affecting the kidney in FMF. Here we present a patient with FMF and membranoproliferative glomerulonephritis and analyze the data published on these two entities.

引用

页码：43 / 45

页数：3

共 16 条

[1]

M680I(Arm2)/M694V(Med) mutations in a patient with familial Mediterranean fever and polyarteritis nodosa [J].

Akpolat, T ;

Yilmaz, E ;

Ozen, S ;

Akpolat, I ;

Danaci, M ;

Kandemir, B .

NEPHROLOGY DIALYSIS TRANSPLANTATION, 1998, 13 (10) :2633-2635

[2]

Familial Mediterranean fever [J].

Ben-Chetrit, E ;

Levy, M .

LANCET, 1998, 351 (9103) :659-664

[3]

ELIAKIM M, 1970, ISRAEL J MED SCI, V6, P228

[4]

SCHONLEIN-HENOCH SYNDROME IN PATIENTS WITH FAMILIAL MEDITERRANEAN FEVER [J].

FLATAU, E ;

KOHN, D ;

SCHILLER, D ;

LURIE, M ;

LEVY, E .

ARTHRITIS AND RHEUMATISM, 1982, 25 (01) :42-47

[5]

Criteria for the diagnosis of familial Mediterranean fever [J].

Livneh, A ;

Langevitz, P ;

Zemer, D ;

Zaks, N ;

Kees, S ;

Lidar, T ;

Migdal, A ;

Padeh, S ;

Pras, M .

ARTHRITIS AND RHEUMATISM, 1997, 40 (10) :1879-1885

[6]

Miller E E, 1976, Rocky Mt Med J, V73, P25

[7]

Polyarteritis nodosa in patients with Familial Mediterranean fever (FMF): A concomitant disease or a feature of FMF? [J].

Ozen, S ;

Ben-Chetrit, E ;

Bakkaloglu, A ;

Gur, H ;

Tinaztepe, K ;

Calguneri, M ;

Turgan, C ;

Turkmen, A ;

Akpolat, I ;

Danaci, M ;

Besbas, N ;

Akpolat, T .

SEMINARS IN ARTHRITIS AND RHEUMATISM, 2001, 30 (04) :281-287

[8]

Familial Mediterranean fever in children: report of a large series and discussion of the risk and prognostic factors of amyloidosis [J].

Saatci, U ;

Ozen, S ;

Ozdemir, S ;

Bakkaloglu, A ;

Besbas, N ;

Topaloglu, R ;

Arslan, S .

EUROPEAN JOURNAL OF PEDIATRICS, 1997, 156 (08) :619-623

[9]

SPECTRUM OF RENAL INVOLVEMENT IN FAMILIAL MEDITERRANEAN FEVER [J].

SAID, R ;

HAMZEH, Y ;

SAID, S ;

TARAWNEH, M ;

ALKHATEEB, M .

KIDNEY INTERNATIONAL, 1992, 41 (02) :414-419

[10]

IGA NEPHROPATHY IN PATIENTS WITH FAMILIAL MEDITERRANEAN FEVER [J].

SAID, R ;

NASRALLAH, N ;

HAMZAH, Y ;

TARAWNEH, M ;

ALKHATIB, M .

AMERICAN JOURNAL OF NEPHROLOGY, 1988, 8 (05) :417-420

← 1 2 →