Fauré P, Chittal S, Woodman-Mêmeteau F, Caverivière P, Gorguet B, Voigt J J, Delsol G
Department of Anatomical Pathology, CHR, Purpan, Toulouse, France.
Cancer. 1988 May 1;61(9):1852-61. doi: 10.1002/1097-0142(19880501)61:9<1852::aid-cncr2820610922>3.0.co;2-0.
Primary malignant lymphomas (ML) of the thyroid are rare and their conclusive morphologic diagnosis is not always possible. The authors report diagnostic features of 11 cases of ML and one case of plasmacytoma of thyroid compared with chronic lymphocytic thyroiditis and undifferentiated carcinomas of thyroid in an immunohistochemical study using monoclonal antibodies (MoAb). The lymphoid nature of tumors could be identified in all cases with three MoAb on paraffin sections. In ML, tumor cells expressed leucocyte common antigen (Dako-LC+) with negativity for epithelial membrane antigen (Dako-EMA-) and cytokeratin (KL1-). Newer MoAb identifying B-cell (LN-1, LN-2, MB2) and T-cell-associated antigens (MT1, UCHL1) not denatured by fixation, revealed B-cell nature of tumor cells in all cases of ML. Among anti-B MoAb, LN-1 and MB2 were most consistent in their reactivity. In cryostat sections of three ML cases, the tumor cells expressed one or more B-cell-associated antigens. Plasmacytoma was negative for Dako-LC and KL1 but positive for Dako-EMA and monotypic cytoplasmic Ig.
甲状腺原发性恶性淋巴瘤(ML)较为罕见,其确切的形态学诊断并非总是可行。作者报告了11例ML及1例甲状腺浆细胞瘤的诊断特征,并在一项使用单克隆抗体(MoAb)的免疫组化研究中,将其与慢性淋巴细胞性甲状腺炎及甲状腺未分化癌进行了比较。在石蜡切片上,使用三种MoAb可在所有病例中识别肿瘤的淋巴样性质。在ML中,肿瘤细胞表达白细胞共同抗原(Dako-LC+),而上皮膜抗原(Dako-EMA-)和细胞角蛋白(KL1-)呈阴性。用于识别未因固定而变性的B细胞(LN-1、LN-2、MB2)和T细胞相关抗原(MT1、UCHL1)的新型MoAb显示,所有ML病例中的肿瘤细胞均为B细胞性质。在抗B MoAb中,LN-1和MB2的反应性最为一致。在3例ML病例的冰冻切片中,肿瘤细胞表达一种或多种B细胞相关抗原。浆细胞瘤Dako-LC和KL1呈阴性,但Dako-EMA和单型细胞质Ig呈阳性。