Cyclosporine in the treatment of an unusual case of juvenile systemic sclerosis.

al-Mayouf, S M; Silverman, E D; Feldman, B M; Thorner, P; Laxer, R M · J Rheumatol · 1998

case_report · Level V

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Abstract

We describe a child who initially presented with juvenile dermatomyositis (JDM). Four years after the complete remission of JDM she developed systemic sclerosis without internal organ involvement. She was unresponsive to a combination of systemic corticosteroid therapy and pencillamine. The institution of cyclosporine induced a complete remission.

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