Mycosis fungoides: Cutaneous T-cell lymphoma

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Abstract

Most patients with mycosis fungoides are between 40 and 60 years of age. The disease has three clinical stages: (1) the premycotic, or patch, stage, consisting of macular, scaling, faint pink to red pruritic patches, usually on unexposed surfaces; (2) the mycotic, or plaque, stage, consisting of reddish, purple-brown plaques, often annular in shape and symmetric in distribution, and (3) the tumor stage, consisting of red-brown to violaceous, dome-shaped, firm tumors with a predilection for the face and body folds. The Sezary syndrome is a leukemic variant. Treatment depends on the extent of disease and includes topical or systemic chemotherapy, radiotherapy and psoralen plus long-wave ultraviolet light therapy.

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Zaim, M. T., & Grinkemeyer, M. D. (1991). Mycosis fungoides: Cutaneous T-cell lymphoma. American Family Physician, 43(5), 1703–1707. https://doi.org/10.5455/2349-3933.ijam20150215

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