[Comparison of clinical features of childhood and adult onset Still's disease]
- PMID: 1767345
[Comparison of clinical features of childhood and adult onset Still's disease]
Abstract
Physical findings, laboratory data, treatments and prognosis were investigated in detail using 26 Japanese childhood Still's disease (CHSD) patients and 19 Japanese adult onset Still's disease (AOSD) patients as the subjects. High spiking fever and arthritis were present in all the patients. Seventy and seven percent of CHSD and 53 percent of AOSD had polyarthritis (the number of joints involved being 5 or more during the first 6 months of the disease). A comparison of the groups showed no significant difference in the initial systemic manifestations except for sore throat (CHSD: AOSD; 19%: 68%). Initial laboratory data were the same for these groups except for serum iron levels (CHSD: AOSD; 20.8 +/- 13.7 micrograms/dl: 83.0 +/- 54.2 micrograms/dl). As to joints and physical prognosis, the results were also the same for CHSD and AOSD under the similar treatment. On the basis of these data, we conclude that CHSD and AOSD are of the same disease entity so far as the present clinical features are concerned.
Similar articles
-
Association of intercellular adhesion molecule-1 with clinical manifestations and interleukin-18 in patients with active, untreated adult-onset Still's disease.Arthritis Rheum. 2005 Jun 15;53(3):320-7. doi: 10.1002/art.21164. Arthritis Rheum. 2005. PMID: 15934126
-
Fever of unknown origin: a review of 20 patients with adult-onset Still's disease.Clin Rheumatol. 2003 May;22(2):89-93. doi: 10.1007/s10067-002-0680-3. Clin Rheumatol. 2003. PMID: 12740670
-
Proinflammatory cytokine profiles in sera and pathological tissues of patients with active untreated adult onset Still's disease.J Rheumatol. 2004 Nov;31(11):2189-98. J Rheumatol. 2004. PMID: 15517632
-
[Adult onset Still's disease].Minerva Med. 2002 Feb;93(1):27-39. Minerva Med. 2002. PMID: 11850612 Review. Italian.
-
Adult Still's disease: part I. Manifestations and complications in sixty-five cases in France.Rev Rhum Engl Ed. 1995 Dec;62(11):748-57. Rev Rhum Engl Ed. 1995. PMID: 8869216 Review.
Cited by
-
Coincident Kikuchi-Fujimoto's disease and adult-onset Still's disease: report of a patient from an uncommonly affected population and case-directed systematic review.Clin Rheumatol. 2021 Dec;40(12):4791-4805. doi: 10.1007/s10067-021-05769-6. Epub 2021 Jun 7. Clin Rheumatol. 2021. PMID: 34100163
-
Management of adult-onset Still's disease with interleukin-1 inhibitors: evidence- and consensus-based statements by a panel of Italian experts.Arthritis Res Ther. 2019 Dec 11;21(1):275. doi: 10.1186/s13075-019-2021-9. Arthritis Res Ther. 2019. PMID: 31829244 Free PMC article.
-
Pathogenesis of adult-onset Still's disease: new insights from the juvenile counterpart.Immunol Res. 2015 Feb;61(1-2):53-62. doi: 10.1007/s12026-014-8561-9. Immunol Res. 2015. PMID: 25388963 Review.
-
Application of the Yamaguchi criteria for classification of "suspected" systemic juvenile idiopathic arthritis (sJIA).Pediatr Rheumatol Online J. 2012 Nov 23;10(1):40. doi: 10.1186/1546-0096-10-40. Pediatr Rheumatol Online J. 2012. PMID: 23176399 Free PMC article.
-
Treatment of adult-onset Still's disease: a review.Ther Clin Risk Manag. 2014 Dec 22;11:33-43. doi: 10.2147/TCRM.S64951. eCollection 2015. Ther Clin Risk Manag. 2014. PMID: 25653531 Free PMC article. Review.
Publication types
MeSH terms
LinkOut - more resources
Other Literature Sources
Medical
Research Materials