A child with a systemic febrile illness - differential diagnosis and management

Best Practice and Research: Clinical Rheumatology

Volumn 20, Issue 4, 2006, Pages 627-640

  Hofer, Michaël ^a   Mahlaoui, Nizar ^b   Prieur, Anne Marie ^b  

^a Paediatric Rheumatology   (Switzerland)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

auto inflammatory diseases; child; diagnosis; fever; inflammation; treatment

Indexed keywords

ACETYLSALICYLIC ACID; ANTIPYRETIC AGENT; COLCHICINE; CORTICOSTEROID; CYCLOSPORIN; IMMUNOGLOBULIN; METHOTREXATE; METHYLPREDNISOLONE; MEVALONATE KINASE; NONSTEROID ANTIINFLAMMATORY AGENT; PENICILLIN G; PREDNISONE; RECOMBINANT INTERLEUKIN 1 RECEPTOR BLOCKING AGENT; STEROID; THALIDOMIDE; TUMOR NECROSIS FACTOR ANTIBODY;

ANGIOFOLLICULAR LYMPH NODE HYPERPLASIA; BEHCET DISEASE; CHILD; CINCA SYNDROME; CLINICAL FEATURE; CLINICAL PROTOCOL; CONNECTIVE TISSUE DISEASE; DIAGNOSTIC PROCEDURE; DIARRHEA; DIFFERENTIAL DIAGNOSIS; DISEASE COURSE; DRUG DOSE REGIMEN; FAMILIAL MEDITERRANEAN FEVER; FEVER; GENE MUTATION; HISTIOCYTOSIS; HUMAN; HYPERIMMUNOGLOBULINEMIA D AND PERIODIC FEVER SYNDROME; INFECTION; INFLAMMATION; JUVENILE RHEUMATOID ARTHRITIS; MORBIDITY; MUCOCUTANEOUS LYMPH NODE SYNDROME; PATHOGENESIS; PFAPA SYNDROME; POLYARTERITIS NODOSA; PRIORITY JOURNAL; PROGNOSIS; RECURRENT DISEASE; REVIEW; SYMPTOM; TREATMENT OUTCOME; VASCULITIS;

CHILD; DIAGNOSIS, DIFFERENTIAL; FEVER OF UNKNOWN ORIGIN; HUMANS; INFLAMMATION; SYNDROME; TIME FACTORS;

EID: 33748451719     PISSN: 15216942     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.berh.2006.04.001     Document Type: Review

References (34)

1. Manners P.J., and Bower C. Worldwide prevalence of juvenile arthritis: why does it vary so much?. The Journal of Rheumatology 29 (2002) 1520-1530
2. Hofer M.F., and Southwood T. Classification of childhood arthritis. Best Practice & Research. Clinical Rheumatology 16 (2002) 379-396
3. Oen K. Comparative epidemiology of the rheumatic diseases in children. Current Opinion in Rheumatology 12 (2000) 410
4. Malleson P.N., Fung M.Y., and Rosenberg A.M. The incidence of paediatric rheumatic diseases: results from the Canadian Paediatric Rheumatology Association Disease Registry. The Journal of Rheumatology 23 (1996) 1981-1987
5. Cobankara V., Fidan G., Turk T., et al. The prevalence of familial Mediterranean fever in the Turkish province of Denizli: a field study with a zero patient design. Clinical and Experimental Rheumatology 22 supplement 34 (2004) S27-S30
6. Hofer M.F., Mouy R., and Prieur A.M. Juvenile idiopathic arthritides evaluated prospectively in a single center according to the Durban criteria. The Journal of Rheumatology 28 (2001) 1083-1090
7. Luthi F., Zufferey P., Hofer M.F., and So A. 'Adolescent-onset Still's disease': characteristics and outcome in comparison with adult-onset Still's disease. Clinical and Experimental Rheumatology 19 (2002) 427-430
8. Rochat I., Sayegh Y., Gervaix A., et al. Acute hypoxic respiratory failure as the first manifestation of systemic-onset juvenile rheumatoid arthritis in a child. Pediatric Pulmonology 38 (2004) 483-487
9. Hofer M.F., Saurenmann T., Ozen S., et al. Pediatric Rheumatology European Society clinical guidelines: systemic arthritis. Pediatric Rheumatology Online Journal 2 (2004) 336-345
10. Quartier P., Taupin P., Bourdeaut F., et al. Efficacy of etanercept for the treatment of juvenile idiopathic arthritis according to the onset type. Arthritis and Rheumatism 48 (2003) 1093-1101
11. Pascual V., Allantaz F., Arce E., et al. Role of interleukin-1 (IL-1) in the pathogenesis of systemic onset juvenile idiopathic arthritis and clinical response to IL-1 blockade. The Journal of Experimental Medicine 201 (2005) 1479-1486
12. Prieur A.M., Roux-Lombard P., and Dayer J.M. Dynamics of fever and the cytokine network in systemic juvenile arthritis. Revue du Rhumatisme (English ed.) 63 (1996) 163-170
13. Guzman J., Fung M., and Petty R.E. Diagnostic value of anti-neutrophil cytoplasmic and anti-endothelial cell antibodies in early Kawasaki disease. The Journal of Pediatrics 124 (1994) 917-920
14. Yeung R. Pathogenesis and treatment of Kawasaki's disease. Current Opinion in Rheumatology 17 (2005) 617-623
15. Criteria for diagnosis of Behcet's disease. International Study Group for Behcet's Disease. Lancet 1990; 335: 1078-1080.
16. David J., Ansell B.M., and Woo P. Polyarteritis nodosa associated with streptococcus. Archives of Disease in Childhood 69 (1993) 685-688
17. Prieur A.M., and Griscelli C. Aspects nosologique des formes systémiques d'arthrite juvénile à début très précoce. A propos de 17 cas. La Semaine des Hôpitaux 60 (1984) 163-167
18. Majeed H.A., El-Khateeb M., El-Shanti H., et al. The spectrum of familial Mediterranean fever gene mutations in Arabs: report of a large series. Seminars in Arthritis and Rheumatism 34 (2005) 813-818
19. Tunca M., Akar S., Onen F., et al., Turkish FMF Study Group. Familial Mediterranean fever (FMF) in Turkey: results of a nationwide multicenter study. Medicine (Baltimore) 84 (2005) 1-11
20. Prieur A.M., Griscelli C., Lampert F., et al. A chronic, infantile, neurological, cutaneous and articular (CINCA) syndrome. A specific entity analysed in 30 patients. Scandinavian Journal of Rheumatology 66 supplement (1987) 57-68
21. Travers R., and Allen R.J. Chronic infantile neurological cutaneous and articular syndrome -- an early description. The Journal of Rheumatology 33 (2006) 822-824
22. Muckle T.J., and Wells M. Urticaria, deafness and amyloidosis: a new heredo-familial syndrome. The Quarterly Journal of Medicine 31 (1962) 235-248
23. Kile R.L., and Rusk H.A. A case of cold urticaria with unusual family history. JAMA 114 (1940) 1067-1068
24. Hoffman H.M., Wright F.A., Broide D.H., et al. Identification of a locus on chromosome 1q44 for familial cold urticaria. American journal of Human Genetics 66 (2000) 1693-1698
25. Feldmann J., Prieur A.M., Quartier P., et al. Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes. American Journal of Human Genetics 71 (2002) 198-203
26. van der Meer J.W.M., Vossen J.M., Radl J., et al. Hyperimmunoglobulinaemia D and periodic fever: a new syndrome. Lancet 323 (1984) 1087-1090
27. Drenth J.P.H., Haagsma C.J., and van der Meer J.W.M. International Hyper-IgD Study Group. Hyperimmunoglobulinemia D and periodic fever syndrome: the clinical spectrum in a series of 50 patients. Medicine 73 (1994) 133-144
28. Houten S.M., Kuis W., Duran M., et al. Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome. Nature Genetics 22 (1999) 175-177
29. Drenth J.P.H., Cuisset L., Grateau G., et al. International Hyper-IgD Study Group. Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. Nature Genetics 22 (1999) 178-181
30. Williamson L.M., Hull D., Mehta R., et al. Familial Hibernian fever. The Quarterly Journal of Medicine 51 (1982) 469-480
31. McDermott M.F., Aksentijevich I., Galon J., et al. Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes. Cell 97 (1999) 133-144
32. Aganna E., Hammond L., Hawkins P.N., et al. Heterogeneity among patients with tumor necrosis factor receptor-associated periodic syndrome phenotypes. Arthritis and Rheumatism 48 (2003) 2632-2644
33. Thomas K.T., Feder Jr. H.M., Lawton A.R., and Edwards K.M. Periodic fever syndrome in children. The Journal of Pediatrics 135 (1999) 15-21
34. Parez N., Bader-Meunier B., Roy C.C., and Dommergues J.P. Paediatric Castleman disease: report of 7 cases and review of the literature. European Journal of Pediatrics 158 (1999) 631-637