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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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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