Sarcoidal tissue reaction in Sézary syndrome - 13/06/12
Doi : 10.1067/mjd.2000.101593
Patrick J. Gregg, MDa, Gary R. Kantor, MDa, Gladys Hines Telang, MDa, Stuart R. Lessin, MDb, Peter C. Nowell, MDc, Eric C. Vonderheid, MDa
Philadelphia, Pennsylvania
From the Departments of Dermatology, MCP Hahnemann University of the Health Sciences,a and the University of Pennsylvania,b Philadelphia, and the Department of Pathology and Laboratory Medicine,c University of Pennsylvania, Philadelphia
Abstract |
Sézary syndrome (SS) is an erythrodermic and leukemic variant of cutaneous T-cell lymphoma (CTCL). Occasionally, the histology of CTCL exhibits evidence of a granulomatous infiltrate in the skin. A case of SS that showed epithelioid granulomas resembling sarcoidosis in the skin and lymph nodes is presented. The clinical course of this patient has been relatively indolent. (J Am Acad Dermatol 2000;43:372-6.)
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 | This supplement is made possible through an educational grant from Ortho Dermatological to the American Academy of Dermatology. |
| Reprint requests: Eric C. Vonderheid, MD, Department of Dermatology, MCP Hahnemann University, MS 478, Broad & Vine St, Philadelphia, PA 19102. E-mail: vonder@evols.com . |
© 2000
American Academy of Dermatology, Inc. Publié par Elsevier Masson SAS. Tous droits réservés.
Vol 43 - N° 2P2
P. 372-376 - août 2000 Retour au numéro
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