Biernat W
Department of Tumour Pathology, Medical School, Lódź.
Pol J Pathol. 1994;45(1):39-44.
This report analysed the phenotype of fourteen cases of Ki-1-positive anaplastic large cell lymphoma, recently described high-grade malignant lymphoma. In 12 cases the neoplasm involved lymph nodes, two patients presented with primary extra-lymphoid involvement (stomach, larynx), whereas secondary involvement of the skin was observed in one patient. Immunohistochemical study revealed B-cell phenotype in seven cases; three cases presented T-cell specific markers; in three cases we found antigens characteristic for both lymphoid lineages and one case presented null phenotype. Ki-1 (CD30) antigen was found in every of 14 cases, and LeuM1 (CD15) antigen was not expressed in any of studied cases. In two cases we revealed the expression of cytokeratins (CAM 5,2). The foregoing results confirm heterogeneity of this neoplasm and suggest careful interpretation of the results of morphologic and immunohistochemical findings in any pleomorphic and anaplastic tumour.
本报告分析了14例Ki-1阳性间变性大细胞淋巴瘤(最近描述的一种高级别恶性淋巴瘤)的表型。12例肿瘤累及淋巴结,2例患者表现为原发性结外受累(胃、喉),而1例患者观察到皮肤继发性受累。免疫组织化学研究显示7例为B细胞表型;3例表现为T细胞特异性标志物;3例发现两种淋巴谱系的特征性抗原,1例表现为无表型。14例均发现Ki-1(CD30)抗原,且所有研究病例均未表达LeuM1(CD15)抗原。2例显示细胞角蛋白(CAM 5,2)表达。上述结果证实了该肿瘤的异质性,并提示对任何多形性和间变性肿瘤的形态学和免疫组织化学结果进行仔细解读。