(See also Overview of Lymphoma.)
Mycosis fungoides and Sézary syndrome are the 2 main types of cutaneous T-cell lymphomas. They comprise less than 5% of all lymphoma cases.
Cutaneous T-cell lymphomas are insidious in onset. Patients may initially present with a chronic, pruritic rash that is difficult to diagnose even with biopsies. This prodrome may exist for several years until the diagnosis of cutaneous T-cell lymphoma is finally made.
The lesions of mycosis fungoides are characterized as patches, plaques, or tumor nodules; the nodules often ulcerate and become infected.
In Sézary syndrome, the skin is typically diffusely red with cracking of the palms and soles. Lymphadenopathy is usually mild to moderate. Symptoms are related mostly to the skin, with fevers, night sweats, and unintentional weight loss coming later in the disease course.
Diagnosis is based on skin biopsy, but histology may be equivocal early in the course because of insufficient quantities of lymphoma cells. The malignant cells are mature CD4+ T cells that may have lost common T-cell markers such as CD7.
Characteristic Pautrier microabscesses are present in the epidermis on skin punch biopsies. In some cases, a leukemic phase called Sézary syndrome is characterized by the appearance of malignant T cells with serpentine nuclei in the peripheral blood. These can be detected on a routine Wright-stained smear or by flow cytometry.
After diagnosis, stage is determined to guide therapy. The commonly used ISCL/EORTC (International Society of Cutaneous Lymphomas/European Organization of Research and Treatment of Cancer) staging system incorporates physical examination findings, histopathology results, and results of imaging tests (1).
1. Olsen E, Vonderheid E, Pimpinelli N, et al: Revisions to the staging and classification of mycosis fungoides and Sezary syndrome: A proposal of the International Society for Cutaneous Lymphomas (ISCL) and the cutaneous lymphoma task force of the European Organization of Research and Treatment of Cancer (EORTC). Blood 110(6):1713–1722, 2007.
Most patients are > 50 years at diagnosis. Survival rates vary markedly depending on stage at diagnosis. Patients who receive treatment for stage IA disease have a life expectancy analogous to that of similar people without mycosis fungoides. Patients with stage II disease have a median survival >5 years, while those diagnosed with stage IV disease survive for just over 2 years.
Treatment can be divided into
Patients are managed by a team of dermatologists, radiation oncologists, and hematology/oncology specialists. Skin-directed therapies are used first and are often effective for years. As lesions become more resistant, oral or IV chemotherapies are used. Lesions may become infected, and the clinician must always consider an infectious cause for any skin flare.
Electron beam radiation therapy, in which most of the energy is absorbed in the first 5 to 10 mm of tissue, and topical nitrogen mustard have proved highly effective. Plaques may also be treated with sunlight and topical corticosteroids.
Systemic treatment with alkylating drugs and folic acid antagonists produces transient tumor regression, but systemic treatment is primarily used when other therapies have failed, after relapse, or in patients with documented extranodal or extracutaneous disease. Newer drugs include HDAC inhibitors given IV or orally. Extracorporeal photophoresis with a chemosensitive drug has shown modest success.
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