Ng C S, Chan J K, Hui P K, Lau W H
Institute of Pathology, Caritas Medical Center, Queen Elizabeth Hospital, Hong Kong.
Hum Pathol. 1989 Dec;20(12):1145-54. doi: 10.1016/s0046-8177(89)80004-8.
Twenty-one cases of large, B-cell lymphoma with an unusually high content of reactive T lymphocytes are described in this report. Fifteen patients presented with lymphoma in nodal sites and six patients presented with lymphoma in extranodal sites. With two exceptions, all patients were more than 50 years of age. The male to female ratio was 1:2. Histologically, isolated to small groups of large lymphoid cells were intermingled with many small lymphocytes. The large cells were neoplastic and exhibited B-lineage markers; immunoglobulin light chain restriction could be demonstrated in two thirds of the cases. There was a rich infiltrate of immunophenotypically mature T lymphocytes that comprised more than 50% of the cellular population. The T lymphocytes ranged from small cells with dark, round nuclei to slightly larger cells with elongated, irregular nuclei. There were occasional medium-sized blastic cells. There was also a variable infiltrate of histiocytes with or without epithelioid features, eosinophils and plasma cells, and increased vascularity. The peculiar morphologic features were also reproduced in other sites in the four patients for whom additional histologic materials were available for examination. We postulate that the abundance of T cells results either from a florid host reaction or from cytokine secretion by the neoplastic B cells, attracting T cells to the vicinity. The morphologic and immunologic features mimic those of a variety of benign lymphoproliferative diseases, angioimmunoblastic lymphadenopathy and lymphomas arising in angioimmunoblastic lymphadenopathy, peripheral T-cell lymphoma, secondary B-immunoblastic lymphoma, and Hodgkin's disease. Careful morphologic evaluation and immunophenotypic studies using leukocyte antibodies reactive in paraffin-embedded sections are of great assistance in determining a diagnosis.
本报告描述了21例反应性T淋巴细胞含量异常高的大B细胞淋巴瘤。15例患者的淋巴瘤位于淋巴结部位,6例患者的淋巴瘤位于结外部位。除2例例外,所有患者年龄均超过50岁。男女比例为1:2。组织学上,孤立的或小群的大淋巴细胞与许多小淋巴细胞混合存在。大细胞为肿瘤性细胞,表现出B细胞系标志物;三分之二的病例可显示免疫球蛋白轻链限制。有丰富的免疫表型成熟T淋巴细胞浸润,占细胞总数的50%以上。T淋巴细胞范围从核暗圆形的小细胞到核细长不规则的稍大细胞。偶尔可见中等大小的母细胞。还有不同程度的组织细胞浸润,有或无上皮样特征、嗜酸性粒细胞和浆细胞,以及血管增多。在另外4例有额外组织学材料可供检查的患者中,其他部位也再现了这种特殊的形态学特征。我们推测T细胞数量丰富要么是由于强烈的宿主反应,要么是由于肿瘤性B细胞分泌细胞因子,将T细胞吸引到附近。其形态学和免疫学特征类似于多种良性淋巴增殖性疾病、血管免疫母细胞性淋巴结病以及由血管免疫母细胞性淋巴结病引起的淋巴瘤、外周T细胞淋巴瘤、继发性B免疫母细胞淋巴瘤和霍奇金病。使用在石蜡包埋切片中有反应的白细胞抗体进行仔细的形态学评估和免疫表型研究,对确定诊断有很大帮助。