Systemic sclerosis in childhood: Clinical and immunologic features of 153 patients in an international database
Article first published online: 28 NOV 2006
Copyright © 2006 by the American College of Rheumatology
Arthritis & Rheumatism
Volume 54, Issue 12, pages 3971–3978, December 2006
How to Cite
Martini, G., Foeldvari, I., Russo, R., Cuttica, R., Eberhard, A., Ravelli, A., Lehman, T. J. A., de Oliveira, S. K. F., Susic, G., Lyskina, G., Nemcova, D., Sundel, R., Falcini, F., Girschick, H., Lotito, A. P., Buoncompagni, A., Sztajnbok, F., Al-Mayouf, S. M., Orbàn, I., Ferri, C., Athreya, B. H., Woo, P. and Zulian, F. (2006), Systemic sclerosis in childhood: Clinical and immunologic features of 153 patients in an international database. Arthritis & Rheumatism, 54: 3971–3978. doi: 10.1002/art.22207
- Issue published online: 28 NOV 2006
- Article first published online: 28 NOV 2006
- Manuscript Accepted: 9 AUG 2006
- Manuscript Received: 6 FEB 2006
To determine the clinical and immunologic features of systemic sclerosis (SSc) in a large group of children and describe the clinical evolution of the disease and compare it with the adult form.
Data on 153 patients with juvenile SSc collected from 55 pediatric rheumatology centers in Europe, Asia, and South and North America were analyzed. Demographic, clinical, and immunologic characteristics of children with juvenile SSc at the onset, at diagnosis, and during the disease course were evaluated.
Raynaud's phenomenon was the most frequent symptom, followed by skin induration in ∼75% of patients. Musculoskeletal symptoms were present in one-third of patients, and the most frequently involved internal organs were respiratory and gastrointestinal, while involvement of renal, cerebral, and cardiovascular systems was extremely rare. Antinuclear antibodies were present in the sera of 81% of patients. Anti–topoisomerase I (Scl-70) and anticentromere antibodies were found to be positive in 34% and 7.1% of patients, respectively. Involvement of the respiratory, gastrointestinal, and cardiovascular systems was more frequent and occurred earlier in patients who died than in those who survived. Compared with the adult form, juvenile SSc appears to be less severe, with the involvement of fewer internal organs, particularly at the time of diagnosis, and has a less characterized immunologic profile.
This study provides information on the largest collection of patients with juvenile SSc ever reported. Juvenile SSc appears to be less severe than in adults because children have less internal organ involvement, a less specific autoantibody profile, and a better long-term outcome.