Weisenburger D D, Nathwani B N, Forman S J, Rappaport H
Cancer. 1982 May 1;49(9):1839-47. doi: 10.1002/1097-0142(19820501)49:9<1839::aid-cncr2820490917>3.0.co;2-z.
We have studied the clinical and pathologic features of three patients with a distinctive non-Hodgkin's lymphoma of the diffuse mixed cell type. The tumors were characterized by a mixture of lymphoid cells of widely varying size and degree of nuclear transformation. A distinctive feature of the neoplastic cells was the presence of cerebriform nuclear contours identical to those seen in mycosis fungoides. Immunologic studies performed on lymph nodes from two patients revealed that the neoplastic cells were T-cells. Characteristic clinical features of the patients were an advanced stage of disease at diagnosis, absence of skin lesions, presence of lung involvement, poor response to aggressive chemotherapy, and a short survival time (9-13 months). The features described closely resemble those of the pleomorphic variant of Japanese adult T-cell leukemia-lymphoma.
我们研究了3例具有独特弥漫性混合细胞型非霍奇金淋巴瘤患者的临床和病理特征。肿瘤的特点是大小和核转化程度差异很大的淋巴细胞混合存在。肿瘤细胞的一个显著特征是存在与蕈样肉芽肿中所见相同的脑回状核轮廓。对2例患者的淋巴结进行的免疫学研究显示,肿瘤细胞为T细胞。这些患者的特征性临床特点为诊断时疾病处于晚期、无皮肤损害、有肺部受累、对积极化疗反应不佳以及生存时间短(9 - 13个月)。所描述的这些特征与日本成人T细胞白血病 - 淋巴瘤的多形性变异型非常相似。