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Lymphocyte-Predominant Hodgkin Lymphoma

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Hodgkin Lymphoma

Part of the book series: Hematologic Malignancies ((HEMATOLOGIC))

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Abstract

Lymphocyte-predominant Hodgkin lymphoma (LPHL) was first described in 1944 by Jackson and Parker as nodular paragranuloma [1]. Other synonyms used were lymphocytic predominant Hodgkin disease, lymphocytic and histiocytic (L&H) predominant Hodgkindisease, nodular lymphocyte-predominant Hodgkin disease, and nodular LPHL [2–5]. This term has become the one that is currently being used. LPHL represents 5% of all HL cases and is a rare disease with an estimated incidence of 1.5 per million [6]. LPHL differs from classical Hodgkin lymphoma in pathological and clinical characteristics.

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Authors and Affiliations

  1. Department of Hematology and Oncology, University Hospital of Cologne, Kerpener Strasse 62, 50924, Köln, Germany

    Andreas Engert

  2. Department of Lymphoma and Myeloma, M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX, 77030, USA

    Anas Younes

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  1. Andreas Engert
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  2. Anas Younes
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Correspondence to Andreas Engert .

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Editors and Affiliations

  1. Klinik I für Innere Medizin, Universität Köln, Joseph-Stelzmann-Str. 9, Köln, 50924, Germany

    Andreas Engert

  2. Dept. Medicine, Stanford University, Stanford, 94305-5479, California, USA

    Sandra J. Horning

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© 2011 Springer-Verlag Berlin Heidelberg

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Engert, A., Younes, A. (2011). Lymphocyte-Predominant Hodgkin Lymphoma. In: Engert, A., Horning, S. (eds) Hodgkin Lymphoma. Hematologic Malignancies. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-12780-9_15

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  • DOI: https://doi.org/10.1007/978-3-642-12780-9_15

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  • Print ISBN: 978-3-642-12779-3

  • Online ISBN: 978-3-642-12780-9

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