Pediatric morphea (localized scleroderma): review of 136 patients.
Détails
ID Serval
serval:BIB_A0E0FB787319
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Pediatric morphea (localized scleroderma): review of 136 patients.
Périodique
Journal of the American Academy of Dermatology
ISSN
1097-6787
Statut éditorial
Publié
Date de publication
2008
Peer-reviewed
Oui
Volume
59
Numéro
3
Pages
385-396
Langue
anglais
Résumé
BACKGROUND: Morphea is an autoimmune inflammatory sclerosing disorder that may cause permanent functional disability and disfigurement. OBJECTIVES: We sought to determine the clinical features of morphea in a large pediatric cohort. METHODS: We conducted a retrospective chart review of 136 pediatric patients with morphea from one center, 1989 to 2006. RESULTS: Most children showed linear morphea, with a disproportionately high number of Caucasian and female patients. Two patients with rapidly progressing generalized or extensive linear morphea and arthralgias developed restrictive pulmonary disease. Initial oral corticosteroid treatment and long-term methotrexate administration stabilized and/or led to disease improvement in most patients with aggressive disease. LIMITATIONS: Retrospective analysis, relatively small sample size, and risk of a selected referral population to the single site are limitations. CONCLUSIONS: These data suggest an increased prevalence of morphea in Caucasian girls, and support methotrexate as treatment for problematic forms. Visceral manifestations rarely occur; the presence of progressive problematic cutaneous disease and arthralgias should trigger closer patient monitoring.
Mots-clé
Adolescent, Age of Onset, Antibodies, Antinuclear, Autoimmune Diseases, Child, Child, Preschool, Dermatologic Agents, European Continental Ancestry Group, Female, Humans, Infant, Male, Methotrexate, Prevalence, Retrospective Studies, Risk Factors, Scleroderma, Localized, Scleroderma, Systemic, Sex Factors, Skin
Pubmed
Web of science
Création de la notice
16/02/2009 11:15
Dernière modification de la notice
20/08/2019 15:06