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Systemic-onset juvenile idiopathic arthritis complicated by early onset amyloidosis in a patient carrying a mutation in the MEFV gene

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Abstract

Systemic juvenile idiopathic arthritis (SJIA) is a disorder characterized by arthritis in children starting before 16 years of age associated with daily high fever, persisting for more than 2 weeks, and at least one of the following clinical features: evanescent cutaneous rash, lymphadenopathy, serositis or hepatosplenomegaly. SJIA patients carry a significantly higher frequency of MEFV mutations, the gene responsible for familial Mediterranean fever, and may be characterized by a more aggressive disease. In this line, we describe a 9-year-old girl affected with SJIA who carried a heterozygous G196W mutation in MEFV. Our patient was characterized by an aggressive disease course, resistance to conventional immunosuppressive agents and developed renal amyloidosis just 2 years after the disease onset.

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References

  1. Petty RE, Southwood TR, Baum J et al (1998) Revision of the proposed classification criteria for juvenile idiopathic arthritis: Durban, 1997. J Rheumatol 25:1991–1994

    PubMed  CAS  Google Scholar 

  2. Petty RE, Southwood TR, Manners P et al (2004) International league of associations for rheumatology classification of juvenile idiopathic arthritis: second revision, Edmonton, 2001. J Rheumatol 31:390–392

    PubMed  Google Scholar 

  3. Lovell DJ (2006) Update on treatment of arthritis in children—new treatments, new goals. Bull Hosp Jt Dis 64:72–76

    Google Scholar 

  4. Pascual V, Allantaz F, Arce E, Punaro M, Banchereau J (2005) Role of interleukin-1 (IL-1) in the pathogenesis of systemic onset juvenile idiopathic arthritis and clinical response to IL-1 blockade. J Exp Med 201:1479–1486

    Article  PubMed  CAS  Google Scholar 

  5. Yokota S, Imagawa T, Mori M et al (2008) Efficacy and safety of tocilizumab in patients with systemic-onset juvenile idiopathic arthritis: a randomised, double-blind, placebo-controlled, withdrawal phase III trial. Lancet 371:998–1006

    Article  PubMed  CAS  Google Scholar 

  6. David J (1991) Amyloidosis in juvenile chronic arthritis. Clin Exp Rheumatol 9:73–78

    PubMed  CAS  Google Scholar 

  7. Immonen K, Savolainen HA, Hakala M (2007) Why can we no longer find juvenile idiopathic arthritis-associated amyloidosis in childhood or in adolescence in Finland? Scand J Rheumatol 36:402–403

    Article  PubMed  CAS  Google Scholar 

  8. Internet periodic fevers (Infevers database). http://fmf.igh.cnrs.fr/infevers

  9. Aganna E, Hawkins PN, Ozen S et al (2004) Allelic variants in genes associated with hereditary periodic fever syndromes as susceptibility factors for reactive systemic AA amyloidosis. Genes Immun 5:289–293

    Article  PubMed  CAS  Google Scholar 

  10. Yeniay BS, Karaca NE, Yuksel SE, Midyat L, Kutukculer N (2007) Juvenile psoriatic arthritis carrying familial Mediterranean fever gene mutations in a 14-year-old Turkish girl. J Dermatol 34:344–348

    Article  PubMed  CAS  Google Scholar 

  11. Ayaz NA, Ozen S, Bilginer Y et al (2009) MEFV mutations in systemic onset juvenile idiopathic arthritis. Rheumatology (Oxford) 48:23–25

    Article  CAS  Google Scholar 

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Correspondence to Luca Cantarini.

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L. Cantarini and O. M. Lucherini contributed equally to this study.

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Cantarini, L., Lucherini, O.M., Simonini, G. et al. Systemic-onset juvenile idiopathic arthritis complicated by early onset amyloidosis in a patient carrying a mutation in the MEFV gene. Rheumatol Int 32, 465–467 (2012). https://doi.org/10.1007/s00296-009-1331-7

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  • DOI: https://doi.org/10.1007/s00296-009-1331-7

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