TY - JOUR
T1 - Methotrexate and corticosteroid therapy for pediatric localized scleroderma
AU - Uziel, Yosef
AU - Feldman, Brian M.
AU - Krafchik, Bernice R.
AU - Yeung, Rae S.M.
AU - Laxer, Ronald M.
PY - 2000
Y1 - 2000
N2 - Introduction: Localized scleroderma (LS) can cause permanent disability, and there is no universally accepted effective treatment. Methotrexate (MTX) has been shown to be effective in the treatment of systemic sclerosis. Objectives: To determine the efficacy and tolerability of MTX and corticosteroid therapy in patients with LS. Methods: MTX, 0.3 to 0.6 mg/kg per week, was given to 10 patients (6 girls, 4 boys; mean age, 6.8 years; mean disease duration before starting treatment, 4 years) with active LS. In addition, pulse intravenous methylprednisolone, 30 mg/kg for 3 days monthly for 3 months, was given to 9 patients at the initiation of therapy. Results: One patient discontinued taking MTX after a month; the remaining 9 patients responded. The median time to response was 3 months (95% CI, 1.15-4.85). One responder discontinued taking MTX after a year because of leukopenia; the LS worsened within 2 months. In another patient LS flared up after 10 months and responded to an increased dose of MTX and intravenous methylprednisolone. At the last follow-up visit, all patients who continued to receive MTX therapy had inactive skin lesions. Conclusion: Treatment with MTX and corticosteroids appears to be effective in the treatment of LS and is generally well tolerated. A placebo-controlled study is necessary to confirm the efficacy of MTX therapy in LS.
AB - Introduction: Localized scleroderma (LS) can cause permanent disability, and there is no universally accepted effective treatment. Methotrexate (MTX) has been shown to be effective in the treatment of systemic sclerosis. Objectives: To determine the efficacy and tolerability of MTX and corticosteroid therapy in patients with LS. Methods: MTX, 0.3 to 0.6 mg/kg per week, was given to 10 patients (6 girls, 4 boys; mean age, 6.8 years; mean disease duration before starting treatment, 4 years) with active LS. In addition, pulse intravenous methylprednisolone, 30 mg/kg for 3 days monthly for 3 months, was given to 9 patients at the initiation of therapy. Results: One patient discontinued taking MTX after a month; the remaining 9 patients responded. The median time to response was 3 months (95% CI, 1.15-4.85). One responder discontinued taking MTX after a year because of leukopenia; the LS worsened within 2 months. In another patient LS flared up after 10 months and responded to an increased dose of MTX and intravenous methylprednisolone. At the last follow-up visit, all patients who continued to receive MTX therapy had inactive skin lesions. Conclusion: Treatment with MTX and corticosteroids appears to be effective in the treatment of LS and is generally well tolerated. A placebo-controlled study is necessary to confirm the efficacy of MTX therapy in LS.
UR - http://www.scopus.com/inward/record.url?scp=0033927514&partnerID=8YFLogxK
U2 - 10.1016/S0022-3476(00)90056-8
DO - 10.1016/S0022-3476(00)90056-8
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C2 - 10636981
AN - SCOPUS:0033927514
SN - 0022-3476
VL - 136
SP - 91
EP - 95
JO - Journal of Pediatrics
JF - Journal of Pediatrics
IS - 1
ER -