Hematopathology Section, Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892, USA.
Cancer J. 2012 Sep-Oct;18(5):411-20. doi: 10.1097/PPO.0b013e31826aee97.
Diffuse large B-cell lymphomas (DLBCLs) are aggressive B-cell lymphomas that are clinically, pathologically, and genetically diverse, in part reflecting the functional diversity of the B-cell system. The focus in recent years has been toward incorporation of clinical features, morphology, immunohistochemistry, and ever evolving genetic data into the classification scheme. The 2008 World Health Organization classification reflects this complexity with the addition of several new entities and variants. The discovery of distinct subtypes by gene expression profiling heralded a new era with a focus on pathways of transformation as well as a promise of more targeted therapies, directed at specific pathways. Some DLBCLs exhibit unique clinical characteristics with a predilection for specific anatomic sites; the anatomic site often reflects underlying biological distinctions. Recently, the spectrum of Epstein-Barr virus (EBV)-driven B-cell proliferations in patients without iatrogenic or congenital immunosuppression has been better characterized; most of these occur in patients of advanced age and include Epstein-Barr virus (EBV)-positive large B-cell lymphoma of the elderly. Human herpesvirus 8 is involved in the pathogenesis of primary effusion lymphoma, which can present as a "solid variant." Two borderline categories were created; one deals with tumors at the interface between classic Hodgkin lymphoma and DLBCL. The second confronts the interface between Burkitt lymphoma and DLBCL, so-called "B-cell lymphoma, unclassifiable, with features intermediate between DLBCL and Burkitt lymphoma" in the 2008 classification. Most cases harbor both MYC and BCL2 translocations and are highly aggressive. Another interesting entity is anaplastic lymphoma kinase-positive DLBCL, which renders itself potentially targetable by anaplastic lymphoma kinase inhibitors. Ongoing investigations at the genomic level, with both exome and whole-genome sequencing, are sure to reveal new pathways of transformation in the future.
弥漫性大 B 细胞淋巴瘤(DLBCL)是一种侵袭性 B 细胞淋巴瘤,在临床、病理和遗传上均具有多样性,部分反映了 B 细胞系统的功能多样性。近年来,人们的关注点一直是将临床特征、形态学、免疫组织化学和不断发展的遗传数据纳入分类方案。2008 年世界卫生组织(WHO)分类通过增加几种新实体和变体反映了这种复杂性。基因表达谱的发现揭示了一个新的时代,其重点是转化途径以及更有针对性的治疗方法,针对特定途径。一些 DLBCL 表现出独特的临床特征,偏爱特定的解剖部位;解剖部位通常反映了潜在的生物学差异。最近,在没有医源性或先天性免疫抑制的情况下,EB 病毒(EBV)驱动的 B 细胞增殖谱得到了更好的描述;这些大多发生在老年患者中,包括老年 EBV 阳性大 B 细胞淋巴瘤。人类疱疹病毒 8 参与了原发性渗出性淋巴瘤的发病机制,其可表现为“实体样”。创建了两个交界类别;一个涉及经典霍奇金淋巴瘤和 DLBCL 之间的肿瘤。第二个涉及 Burkitt 淋巴瘤和 DLBCL 之间的界面,在 2008 年的分类中被称为“无分类特征的 B 细胞淋巴瘤,介于 DLBCL 和 Burkitt 淋巴瘤之间”。大多数病例均存在 MYC 和 BCL2 易位,且侵袭性高。另一个有趣的实体是间变性淋巴瘤激酶阳性 DLBCL,它可通过间变性淋巴瘤激酶抑制剂靶向治疗。在基因组水平上进行的外显子组和全基因组测序等正在进行的研究肯定会在未来揭示新的转化途径。