Cutaneous T-Cell Lymphomas: The Sézary Syndrome, Mycosis Fungoides, and Related Disorders

  1. MARVIN LUTZNER, M.D.;
  2. RICHARD EDELSON, M.D.;
  3. PHILIP SCHEIN, M.D., F.A.C.P.;
  4. IRA GREEN, M.D.;
  5. CHARLES KIRKPATRICK, M.D.; and
  6. AFTAB AHMED, Ph.D.
  1. Bethesda, Maryland

    Abstract

    Substantial evidence has accumulated to indicate not only that mycosis fungoides and the Sézary syndrome are closely related malignancies, but to suggest that they are part of a larger spectrum of cutaneous lymphomas. The neoplastic cells of these disorders have membrane features of thymus-derived (T) lymphocytes, a characteristic tissue distribution (skin infiltration, marrow sparing, localization in T-cell regions of lymphoid tissue), and distinctive morphology. For these reasons, we suggest that these lymphoproliterative disorders be grouped together as "cutaneous T-cell lymphomas." The anergy noted in patients of this group with leukemia probably is related to both decreased percentages of normal T cells and presence in the serum of macrophage migration inhibitory activity. Leukapheresis has been particularly effective in the management of selected patients. The homogeneous T-cell populations in the patients with leukemia also provide important opportunities to study many aspects of lymphocyte physiology that are of broad biologic significance.

    Article and Author Information

    • ▸An edited transcription of a Combined Clinical Staff Conference at the Clinical Center, Bethesda, Maryland, 12 September 1974, by the National Cancer Institute, National Institutes of Health, U.S. Department of Health, Education, and Welfare.

    • ▸Requests for reprints should be addressed to Marvin A. Lutzner, M.D., Chief, Dermatology Branch, National Cancer Institute, Bldg. 10, Room 12N-238, National Institutes of Health, Bethesda, MD 20014.

      • Received July 15, 1975.
      • Accepted July 22, 1975.
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