Skip to main content
Top
Published in: Pediatric Nephrology 11/2005

01-11-2005 | Rapid Communication

IgA nephropathy in an Italian child with familial Mediterranean fever

Authors: Donato Rigante, Gilda Federico, Pietro Ferrara, Nicola Maggiano, Laura Avallone, Anna Lisa Pugliese, Achille Stabile

Published in: Pediatric Nephrology | Issue 11/2005

Login to get access

Abstract

Familial Mediterranean fever is an autosomal recessive disorder characterized by transient attacks of fever and polyserositis with substantial risk of developing amyloidotic nephropathy over time. We report an Italian child with familial Mediterranean fever presenting with hematuria during attacks in whom kidney biopsy documented the presence of mesangial IgA deposits and the absence of amyloidosis. Kidney biopsy should be performed in patients showing microscopic or gross hematuria during attacks of familial Mediterranean fever in order to gain additional epidemiological data about specific features of renal involvement and to allow adequate treatment.
Literature
1.
go back to reference Sohar E, Gafni J, Pras M, Heller H (1967) Familial Mediterranean fever. A survey of 470 cases and review of the literature. Am J Med 43:227–253CrossRefPubMed Sohar E, Gafni J, Pras M, Heller H (1967) Familial Mediterranean fever. A survey of 470 cases and review of the literature. Am J Med 43:227–253CrossRefPubMed
2.
go back to reference Eliakim M (1970) Incidence of amyloidosis in recurrent polyserositis (familial Mediterranean fever). Isr J Med Sci 6:2–8PubMed Eliakim M (1970) Incidence of amyloidosis in recurrent polyserositis (familial Mediterranean fever). Isr J Med Sci 6:2–8PubMed
3.
go back to reference Sachs D, Langevitz P, Morag B, Pras M (1987) Polyarteritis nodosa and familial Mediterranean fever. B J Rheumatol 26:139–141 Sachs D, Langevitz P, Morag B, Pras M (1987) Polyarteritis nodosa and familial Mediterranean fever. B J Rheumatol 26:139–141
4.
go back to reference Schlesinger M, Kopolovic J, Viskoper RJ, Ron N (1983) A case of familial Mediterranean fever with cutaneous vasculitis and immune complex nephritis: light, electron and immunofluoresceint study of renal biopsy. Am J Clin Pathol 80:511–514PubMed Schlesinger M, Kopolovic J, Viskoper RJ, Ron N (1983) A case of familial Mediterranean fever with cutaneous vasculitis and immune complex nephritis: light, electron and immunofluoresceint study of renal biopsy. Am J Clin Pathol 80:511–514PubMed
5.
go back to reference Tsimaratos M, Koné-Paut I, Daniel L, Gubler M-C, Dussol B, Picon G. (1999) Crescentic glomerulonephritis in hyper IgD syndrome. Pediatr Nephrol 13:132–134CrossRefPubMed Tsimaratos M, Koné-Paut I, Daniel L, Gubler M-C, Dussol B, Picon G. (1999) Crescentic glomerulonephritis in hyper IgD syndrome. Pediatr Nephrol 13:132–134CrossRefPubMed
6.
go back to reference Churg J, Bernstein J, Glassock RJ (1995) Renal disease: classification and atlas of glomerular diseases, 2nd edn. Igaku-Shoin Medical Publishers, Tokyo, pp 86–88 Churg J, Bernstein J, Glassock RJ (1995) Renal disease: classification and atlas of glomerular diseases, 2nd edn. Igaku-Shoin Medical Publishers, Tokyo, pp 86–88
7.
go back to reference Ozdogan H, Arisoy N, Kasapçapur O, Sever L, Çalişkan S, Tuzuner N, Mat C, Yazici H (1997) Vasculitis in familial Mediterranean fever. J Rheumatol 24:323–327PubMed Ozdogan H, Arisoy N, Kasapçapur O, Sever L, Çalişkan S, Tuzuner N, Mat C, Yazici H (1997) Vasculitis in familial Mediterranean fever. J Rheumatol 24:323–327PubMed
8.
go back to reference Heller H, Sohar E, Sherf L (1958) Familial Mediterranean fever. Arch Int Med 102:50–71 Heller H, Sohar E, Sherf L (1958) Familial Mediterranean fever. Arch Int Med 102:50–71
9.
go back to reference International FMF Consortium (1997) Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. Cell 90:797–807CrossRefPubMed International FMF Consortium (1997) Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. Cell 90:797–807CrossRefPubMed
10.
go back to reference The French FMF Consortium (1997) A candidate gene for familial Mediterranean fever. Nature Genet 17:25–31CrossRefPubMed The French FMF Consortium (1997) A candidate gene for familial Mediterranean fever. Nature Genet 17:25–31CrossRefPubMed
11.
go back to reference Said R, Hamzeh Y, Said S, Tarawneh M, Al-Khateeb M (1992) Spectrum of renal involvement in familial Mediterranean fever. Kidney Int 41:414–419PubMed Said R, Hamzeh Y, Said S, Tarawneh M, Al-Khateeb M (1992) Spectrum of renal involvement in familial Mediterranean fever. Kidney Int 41:414–419PubMed
12.
go back to reference Heller H, Sohar E, Gafni J, Heller J (1961) Amyloidosis in familial Mediterranean fever. An independent genetically determined character. Arch Intern Med 107:539–550PubMed Heller H, Sohar E, Gafni J, Heller J (1961) Amyloidosis in familial Mediterranean fever. An independent genetically determined character. Arch Intern Med 107:539–550PubMed
13.
go back to reference Pras M, Bronshpigel N, Zemer D, Gafni J. (1982)Variable incidence of amyloidosis in familial Mediterranean fever among different ethnic groups. Johns Hopkins Med J 150:22–26PubMed Pras M, Bronshpigel N, Zemer D, Gafni J. (1982)Variable incidence of amyloidosis in familial Mediterranean fever among different ethnic groups. Johns Hopkins Med J 150:22–26PubMed
14.
go back to reference Ehrenfeld EN, Eliakim M, Rachmilewitz M (1970) Recurrent polyserositis (familial Mediterranean fever; periodic disease). A report of 55 cases. Am J Med 31:107–123CrossRef Ehrenfeld EN, Eliakim M, Rachmilewitz M (1970) Recurrent polyserositis (familial Mediterranean fever; periodic disease). A report of 55 cases. Am J Med 31:107–123CrossRef
15.
go back to reference Reimann HA, Moadie J, Semerdjian S, Sahyoun PF (1954) Periodic peritonitis—heredity and pathology. Report of 72 cases. J Am Med Assoc 154:1254–1259PubMed Reimann HA, Moadie J, Semerdjian S, Sahyoun PF (1954) Periodic peritonitis—heredity and pathology. Report of 72 cases. J Am Med Assoc 154:1254–1259PubMed
16.
go back to reference La Regina M, Nucera G, Diaco M, Procopio A, Gasbarrini G, Notarnicola C, Kone-Paut I, Touitou I, Manna R (2003) Familial Mediterranean fever is no longer a rare disease in Italy. Eur J Hum Genet 11:50–56CrossRefPubMed La Regina M, Nucera G, Diaco M, Procopio A, Gasbarrini G, Notarnicola C, Kone-Paut I, Touitou I, Manna R (2003) Familial Mediterranean fever is no longer a rare disease in Italy. Eur J Hum Genet 11:50–56CrossRefPubMed
17.
go back to reference Eliakim M, Rachmilewitz M, Rosenmann E, Niv A (1970) Renal manifestations in recurrent polyserositis (familial Mediterranean fever). Isr J Med Sci 6:228–245PubMed Eliakim M, Rachmilewitz M, Rosenmann E, Niv A (1970) Renal manifestations in recurrent polyserositis (familial Mediterranean fever). Isr J Med Sci 6:228–245PubMed
18.
go back to reference Flatau E, Kohn D, Schiller D, Lune M, Levy E (1982) Henoch-Schönlein syndrome in patients with familial Mediterranean fever. Arthritis Rheum 25:42–47PubMed Flatau E, Kohn D, Schiller D, Lune M, Levy E (1982) Henoch-Schönlein syndrome in patients with familial Mediterranean fever. Arthritis Rheum 25:42–47PubMed
19.
go back to reference Said R, Nasrallah N, Hamzeh Y, Tarawneh M, Al-Khatib M (1988) IgA nephropathy in patients with familial Mediterranean fever. Am J Nephrol 8:417–420PubMed Said R, Nasrallah N, Hamzeh Y, Tarawneh M, Al-Khatib M (1988) IgA nephropathy in patients with familial Mediterranean fever. Am J Nephrol 8:417–420PubMed
20.
go back to reference Tekin M, Yalçinkaya F, Tümer N, Çakar N, Koçak H, Özkaya N, Gençgönül H (1999) Familial Mediterranean fever—renal involvement by diseases other than amyloid. Nephrol Dial Transplant 14:475–479CrossRefPubMed Tekin M, Yalçinkaya F, Tümer N, Çakar N, Koçak H, Özkaya N, Gençgönül H (1999) Familial Mediterranean fever—renal involvement by diseases other than amyloid. Nephrol Dial Transplant 14:475–479CrossRefPubMed
21.
go back to reference Akpolat T, Akpolat I, Karagoz F, Yilmaz E, Kandemir B, Ozen S (2004) Familial Mediterranean fever and glomerulonephritis and review of the literature. Rheumatol Int 24:43–45CrossRefPubMed Akpolat T, Akpolat I, Karagoz F, Yilmaz E, Kandemir B, Ozen S (2004) Familial Mediterranean fever and glomerulonephritis and review of the literature. Rheumatol Int 24:43–45CrossRefPubMed
22.
go back to reference Koukoui L, Blau A, Kopolovic J, Pras M, Livneh A (2004) A possible favourable effect of colchicine in IgA nephropathy on a carrier of a MEFV mutation. Clin Nephrol 62:226–228PubMed Koukoui L, Blau A, Kopolovic J, Pras M, Livneh A (2004) A possible favourable effect of colchicine in IgA nephropathy on a carrier of a MEFV mutation. Clin Nephrol 62:226–228PubMed
Metadata
Title
IgA nephropathy in an Italian child with familial Mediterranean fever
Authors
Donato Rigante
Gilda Federico
Pietro Ferrara
Nicola Maggiano
Laura Avallone
Anna Lisa Pugliese
Achille Stabile
Publication date
01-11-2005
Publisher
Springer-Verlag
Published in
Pediatric Nephrology / Issue 11/2005
Print ISSN: 0931-041X
Electronic ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-005-2023-5

Other articles of this Issue 11/2005

Pediatric Nephrology 11/2005 Go to the issue

Announcements

November 2005