Pediatric morphea (localized scleroderma): Review of 136 patients

BackgroundMorphea is an autoimmune inflammatory sclerosing disorder that may cause permanent functional disability and disfigurement.ObjectivesWe sought to determine the clinical features of morphea in a large pediatric cohort.MethodsWe conducted a retrospective chart review of 136 pediatric patients with morphea from one center, 1989 to 2006.ResultsMost 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.LimitationsRetrospective analysis, relatively small sample size, and risk of a selected referral population to the single site are limitations.ConclusionsThese 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.