Hussaini Mohammad O, Kreisel Friederike H, Hassan Anjum, Nguyen TuDung T, Frater John L
Mohammad O Hussaini, Division of Molecular Pathology, Department of Pathology and Immunology, Washington University in St. Louis School of Medicine, St. Louis, MO 63110, United States.
World J Methodol. 2016 Sep 26;6(3):181-6. doi: 10.5662/wjm.v6.i3.181.
CD4 expression is rare in diffuse large B-cell lymphoma (DLBCL), with 4 previously reported cases. Its significance is uncertain. We report five patients with CD4(+) DLBCL and one CD4(+) primary mediastinal large B-cell lymphoma. Cases were identified by searching the electronic database of the department; each was reviewed. Average age was 56 years. Neoplastic cells expressed CD20 (5/6 tested cases). BCL2/BCL6 expression were seen in 3/3 tested cases, suggesting a germinal center origin. Additionally, expression of T-cell antigens CD2 and CD5 was noted in 2/2 and CD7 in 1/1 tested case. CD3 was negative in all. Lymph nodes were commonly involved (67%). Patients received chemotherapy +/- radiation (6/6) and bone marrow transplant (2/6). Average survival was 44.2 mo. CD4 expression in DLBCL raises questions of lineage commitment. CD4(+) DLBCL is rare; care should be exercised not to diagnose these as T-cell lymphomas. A subset behaves aggressively.
CD4表达在弥漫性大B细胞淋巴瘤(DLBCL)中罕见,此前仅有4例报道。其意义尚不确定。我们报告了5例CD4(+)弥漫性大B细胞淋巴瘤患者和1例CD4(+)原发性纵隔大B细胞淋巴瘤患者。通过检索科室电子数据库确定病例;对每例病例进行了复查。平均年龄为56岁。肿瘤细胞表达CD20(5/6例检测病例)。在3/3例检测病例中可见BCL2/BCL6表达,提示生发中心起源。此外,在2/2例检测病例中发现T细胞抗原CD2和CD5表达,在1/1例检测病例中发现CD7表达。所有病例中CD3均为阴性。淋巴结常受累(67%)。患者接受了化疗±放疗(6/6)和骨髓移植(2/6)。平均生存期为44.2个月。DLBCL中的CD4表达引发了细胞系定向的问题。CD4(+)弥漫性大B细胞淋巴瘤罕见;应注意不要将这些病例诊断为T细胞淋巴瘤。一部分病例行为侵袭性。