Seminars in Radiation Oncology
Volume 17, Issue 3 , Pages 184-189, July 2007

Nodular Lymphocyte-Predominant Hodgkin Lymphoma

  • Henry K. Tsai, MD
  • ,
  • Peter M. Mauch, MD

      Affiliations

    • Corresponding Author InformationAddress reprint requests to Peter M. Mauch, MD, Department of Radiation Oncology, Brigham and Women’s Hospital, 75 Francis Street, Boston, MA 02115.

Department of Radiation Oncology, Brigham and Women’s Hospital and Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.

Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL), a distinct subtype of Hodgkin lymphoma, is a rare disease with a generally favorable prognosis. The hallmark of NLPHL is the presence of the lymphocytic and histiocytic cell, which, in contrast to the classic Reed-Sternberg cell, is CD20+, CD15−, and CD30−. NLPHL tends to have an indolent natural history, a long time to disease progression, a delayed time to relapse, and a high likelihood of presenting as early-stage disease. The evidence to guide the management of patients with NLPHL is limited by the rarity of this disease, but the available data support the use of involved-field radiation therapy alone for localized disease. Treatment-related late effects contribute significantly to the causes of death in patients treated for NLPHL.

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PII: S1053-4296(07)00015-X

doi:10.1016/j.semradonc.2007.02.004

Seminars in Radiation Oncology
Volume 17, Issue 3 , Pages 184-189, July 2007