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Article
August 1977

Eosinophilic Fasciitis

Author Affiliations

From the Rheumatology Section (Dr Krauser) and Department of Pathology (Dr Tuthill), Naval Regional Medical Center, Portsmouth, Va.

Arch Dermatol. 1977;113(8):1092-1093. doi:10.1001/archderm.1977.01640080094017
Abstract

• A detailed evaluation of the clinical and histologic manifestations of eosinophilic fasciitis is described in a 22-year-old woman. Scleroderma-like skin involvement is associated with eosinophilia and hypergammaglobulinemia. Visceral and serologic manifestations of a generalized scleroderma are lacking. Results of a biopsy showed severe thickening of the deep fascia accompanied by an infiltration of lymphocytes and plasma cells. This syndrome must be differentiated from generalized scleroderma because eosinophilic fasciitis has a benign course and may benefit from systemic corticosteroid therapy.

(Arch Dermatol 113:1092-1093, 1977)

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