Eosinophilic Fasciitis: A Case Report and Literature Review

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Charussri Leeyaphan
Kanokvalai Kulthanan
Panitta Sitthinamsuwan
Nisa Kiewjoy

Abstract

Eosinophilic fasciitis (EF) is a rare scleroderma-like syndrome. There has been no previous published report of EF in a Thai patient. We described a 41 year-old Thai man who presented with symmetric induration of the skin of forearms, arms, hands, fingers, lower aspects of the legs, and feet. Physical examination revealed bilateral symmetrical woody induration of the skin with peau d’orange appearance. A groove sign was positive on the flexural surface of both arms. Laboratory testing revealed a peripheral eosinophil count of 54%. The skin and superficial fascia biopsy specimen from the inner aspect of the left forearm was consistent with EF. He was treated with prednisolone, methotrexate, and colchicine. He experienced a gradual improvement within 4 months. A history of acute onset of scleroderma-like syndrome and careful physical examination can lead us to the diagnosis of EF.

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How to Cite
Leeyaphan, C. ., Kulthanan, K. ., Sitthinamsuwan, . P. ., & Kiewjoy, N. . (2020). Eosinophilic Fasciitis: A Case Report and Literature Review. Siriraj Medical Journal, 62(4), 173–175. Retrieved from https://he02.tci-thaijo.org/index.php/sirirajmedj/article/view/243896
Section
Case Report