Li Jing, Zhao Shu, Wang Jingxuan, Chen Jingyu, Wen Wen, Zhang Qingyuan
Department of Internal Medicine, The Third Affiliated Hospital of Harbin Medical University, Haping Road 150 of Nangang District, Harbin, Heilongjiang Province, 150081, China.
Department of Internal Medicine, The Fourth Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province, 150081, China.
Tumour Biol. 2016 Mar;37(3):3619-37. doi: 10.1007/s13277-015-4205-5. Epub 2015 Oct 12.
CD20 expression is absent in a variety of diffuse large B cell lymphomas (DLBCLs), including plasmablastic lymphoma, primary effusion lymphoma, anaplastic lymphoma, kinase-positive DLBCL, and large B cell lymphoma arising in human herpesvirus 8-associated multicentric Castleman disease. These rare and heterogeneous tumors are characterized by the presence of proliferating immunoblasts with similar transcriptional profiles as those of plasma cells and are typically associated with highly aggressive pathologies, with high levels of chemotherapy resistance and low survival rates; thus, they pose significant diagnostic and treatment challenges. We conducted a systematic literature review of the limited existing clinical data to summarize the current knowledge regarding the biological basis, diagnostic limits, and potential therapeutic targets of distinct variants of CD20-negative DLBCL. This review will hopefully increase the awareness of these rare disorders among clinicians and pathologists and prompt basic and clinical research.
CD20表达在多种弥漫性大B细胞淋巴瘤(DLBCL)中缺失,包括浆母细胞性淋巴瘤、原发性渗出性淋巴瘤、间变性淋巴瘤、激酶阳性DLBCL以及人类疱疹病毒8相关多中心Castleman病中发生的大B细胞淋巴瘤。这些罕见且异质性的肿瘤特征为存在增殖的免疫母细胞,其转录谱与浆细胞相似,通常与高度侵袭性病理相关,化疗耐药水平高且生存率低;因此,它们带来了重大的诊断和治疗挑战。我们对有限的现有临床数据进行了系统的文献综述,以总结关于CD20阴性DLBCL不同变体的生物学基础、诊断局限和潜在治疗靶点的当前知识。本综述有望提高临床医生和病理学家对这些罕见疾病的认识,并促进基础和临床研究。