Department of Medical Oncology, British Columbia Cancer Agency, Vancouver, BC, Canada.
Br J Haematol. 2013 May;161(3):316-29. doi: 10.1111/bjh.12244. Epub 2013 Feb 8.
Nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) represents 5% of all Hodgkin lymphoma and has distinct clinico-pathological features. It is typified by the presence of lymphocyte predominant cells, which are CD20(+) , CD15(-) and CD30(-) and are found scattered amongst small B-lymphocytes arranged in a nodular pattern. Patients typically are males presenting with localized, peripheral lymphadenopathy. Despite frequent and often late or multiple relapses the prognosis is favourable. Deaths due to NLPHL are uncommon, but secondary malignancies and other treatment toxicities contribute appreciably to overall mortality. Secondary aggressive non-Hodgkin lymphoma can occur in approximately 7-14% of cases of NLPHL. Given this diseases' rarity, the optimal management is unclear and opinions differ as to whether treatment paradigms should be similar to or differ from those for classical Hodgkin lymphoma. This review provides an overview of the existing literature describing of the outcome and treatment approaches for limited and advanced stage NLPHL.
结节性淋巴细胞为主型霍奇金淋巴瘤(NLPHL)占所有霍奇金淋巴瘤的 5%,具有独特的临床病理特征。其特征在于存在淋巴细胞为主的细胞,这些细胞 CD20(+)、CD15(-)和 CD30(-),散布在呈结节状排列的小 B 淋巴细胞之间。患者通常为男性,表现为局限性、外周淋巴结病。尽管经常发生且往往延迟或多次复发,但预后良好。NLPHL 导致的死亡并不常见,但继发性恶性肿瘤和其他治疗毒性对总死亡率有相当大的影响。继发性侵袭性非霍奇金淋巴瘤在 NLPHL 病例中约占 7-14%。由于这种疾病的罕见性,其最佳治疗方法尚不清楚,对于治疗方案是否应该与经典霍奇金淋巴瘤相似或不同存在不同意见。本综述概述了描述局限性和晚期 NLPHL 的结局和治疗方法的现有文献。