been training intensively during the preceding 3 months. Examination revealed markedly indurated skin affecting the extremities. There was a decreased range of movement in the wrists and ankles (bilaterally). He could not fully clench his fist with either hand.A skin punch biopsy revealed prominent thickening of the collagen bundles throughout the dermis with a reduction in fibroblast numbers and a perivascular inflammatory infiltrate with scant eosinophils. There was a blood eosinophilia of 1.49 × 10 9 /L (normal range = 0.04 -0.4 × 10 9 /L). The clinical impression was that of generalized cutaneous scleroderma with features of eosinophilic fasciitis. High-dose prednisolone and hydroxychloroquine were commenced for 6 months. However, indurated patches of scleroderma spread to the trunk and his joints remained as before.Methotrexate at a dose of 15 mg once weekly was then commenced. There was little change after 2 months, and so psoralen-ultraviolet A therapy (PUVA) at a dose of 0.6mg/kg twice weekly was added, based on reports of its effectiveness in the literature. 1-3 The risk of non-melanotic skin cancers when combining immunosuppressive and PUVA therapy was considered. It was felt that this treatment was warranted in light of the significant limitation of mobility and potential for development of contractures. The risks were explained to the patient.PUVA treatment was continued for 20 sessions over 10 weeks at a cumulative dose of 25.4 J/cm 2 . Methotrexate was subsequently administered for 7 months. After this period he was able to make a full fist and normal range of movement in the ankles was achieved. The skin had returned to normal consistency and pigmentation. He has maintained clinical remission for 2 years.Cutaneous scleroderma is caused by the interaction between skin-infiltrating T-helper cells and dermal fibroblasts. The histological pattern includes cellular infiltrates of lymphocytes, plasma cells and eosinophils. The dermis is thickened with dense collagen, scant fibroblasts and reduced elastic tissue. Laboratory investigations may reveal a raised erythrocyte sedimentation rate, eosinophilia and hypocomplementaemia. Contractures and limb atrophy may occur.Eosinophilic fasciitis occurs more commonly in male subjects and can follow strenuous exertion. Haematic eosinophilia occurs frequently. Spontaneous remission may occur. Eosinophilic fasciitis and cutaneous scleroderma have been linked in the literature. One report suggests that eosinophilic fasciitis may be a steroid-responsive variant of scleroderma. 4 This patient had features of both clinical entities. The microscopical findings are compatible with either process. The lack of response to steroids and lack of spontaneous improvement are more suggestive of generalized cutaneous scleroderma.The rapid response to PUVA and methotrexate 2 years after onset of disease indicates that these treatments were highly effective, and successfully reversed generalized cutaneous scleroderma. Methotrexate has also been reported to be therapeutic in widespre...