Gupta Neha, Nasim Mansoor, Spitzer Silvia G, Zhang Xinmin
1 Hofstra Northwell School of Medicine, Lake Success, NY, USA.
Int J Surg Pathol. 2017 Oct;25(7):599-603. doi: 10.1177/1066896917714325. Epub 2017 Jun 14.
Primary central nervous system T-cell lymphoma (PCNSTCL) is rare, accounting for 2% of CNS lymphomas. We report the first case of PCNSTCL with aberrant expression of CD20 and CD79a in an 81-year-old man with a left periventricular brain mass. A biopsy revealed dense lymphoid infiltrate consisting of medium-sized cells in a background of gliosis and many histiocytes. The lymphoid cells were positive for CD2, CD3, CD7, CD8, T-cell intracellular antigen-1, granzyme B, CD20, and CD79a and negative for CD4, CD5, PAX-5, OCT-2, BOB-1, human herpes virus-8, and Epstein-Barr virus-encoded small RNAs. Molecular studies revealed clonal TCR-β and TCR-γ gene rearrangements and negative immunoglobulin gene rearrangements. The patient was treated with chemotherapy (vincristine and methotrexate) and rituximab, but he died 1 month after the diagnosis. This is a unique case that emphasizes the use of a multimodal approach, including a broad immunohistochemical panel and molecular studies in lineage determination for lymphomas with ambiguous phenotype.
原发性中枢神经系统T细胞淋巴瘤(PCNSTCL)较为罕见,占中枢神经系统淋巴瘤的2%。我们报告了首例发生于一名81岁男性、伴有左侧脑室周围脑肿块且CD20和CD79a表达异常的PCNSTCL病例。活检显示在胶质增生和许多组织细胞背景下,有由中等大小细胞组成的密集淋巴样浸润。淋巴样细胞CD2、CD3、CD7、CD8、T细胞胞内抗原-1、颗粒酶B、CD20和CD79a呈阳性,而CD4、CD5、PAX-5、OCT-2、BOB-1、人类疱疹病毒8型和爱泼斯坦-巴尔病毒编码的小RNA呈阴性。分子研究显示克隆性TCR-β和TCR-γ基因重排,免疫球蛋白基因重排阴性。该患者接受了化疗(长春新碱和甲氨蝶呤)及利妥昔单抗治疗,但在诊断后1个月死亡。这是一个独特的病例,强调了采用多模式方法的重要性,包括使用广泛的免疫组织化学检测组以及对表型不明确的淋巴瘤进行谱系确定的分子研究。