Abstract
Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) is a rare disease constituting only 3-8% of all Hodgkin lymphoma. It has a distinct histological and clinical presentation as well as significantly different natural history compared to the classical form of Hodgkin lymphoma. Presenting most often as early-stage disease, NLPHL is characterized by frequent relapses, but paradoxically an overall good prognosis. The approach to management should therefore reflect this pattern and focus on attaining prolonged remissions, with long-term follow-up paramount. Due to the rarity of the disease, few prospective data exist. Options for treatment include radiotherapy, chemotherapy or combined chemotherapy plus radiotherapy and targeted anti-CD20 antibody therapy, as well as observation in selected patients.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Antibodies, Monoclonal, Murine-Derived / therapeutic use
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Antineoplastic Combined Chemotherapy Protocols / administration & dosage
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use
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Bleomycin / administration & dosage
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Clinical Trials as Topic
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Dacarbazine / administration & dosage
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Doxorubicin / administration & dosage
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Histiocytes / pathology
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Hodgkin Disease / classification
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Hodgkin Disease / diagnosis
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Hodgkin Disease / epidemiology
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Hodgkin Disease / pathology*
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Hodgkin Disease / therapy
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Humans
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Immunophenotyping
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Lymph Node Excision
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Lymphatic Irradiation / methods
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Lymphocytes / pathology
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Prognosis
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Recurrence
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Rituximab
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Salvage Therapy
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Vinblastine / administration & dosage
Substances
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Antibodies, Monoclonal, Murine-Derived
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Bleomycin
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Rituximab
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Vinblastine
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Dacarbazine
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Doxorubicin