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B 细胞和 T 细胞型侵袭性恶性淋巴瘤的脾脏受累:一项形态学和免疫表型研究。

Splenic involvement by aggressive malignant lymphomas of B-cell and T-cell types. A morphologic and immunophenotypic study.

作者信息

Stroup R M, Burke J S, Sheibani K, Ben-Ezra J, Brownell M, Winberg C D

机构信息

James Irvine Center for the Study of Leukemia and Lymphoma, Division of Pathology, City of Hope National Medical Center, Duarte, California.

出版信息

Cancer. 1992 Jan 15;69(2):413-20. doi: 10.1002/1097-0142(19920115)69:2<413::aid-cncr2820690223>3.0.co;2-j.

Abstract

To determine whether there are any consistent morphologic differences between B-cell and T-cell aggressive non-Hodgkin's lymphomas of the spleen, the authors analyzed 16 spleens involved by mixed cell (1 case) or large cell (15 cases) lymphomas. Immunologic data were derived from cell suspensions or frozen tissue in each case. Five cases had a T-cell phenotype, and 11 were B-cell. Morphologic features favoring a T-cell phenotype included epithelioid histiocytic reactions, confinement of the lymphomas to the splenic T-zones (periarteriolar lymphoid sheath and marginal zone), and clear cell or polymorphous cytologic features. Features favoring a B-cell phenotype included multiple discrete nodules in the white pulp, large coalescent tumor nodules in association with small lymphocytic lymphoma, and large non-cleaved or immunoblastic plasmacytoid cytologic characteristics. Four cases were unusual because most neoplastic large cells were distributed diffusely or formed only small aggregates in the red pulp without definite tumor masses or nodules involving the white pulp. Because of this distribution and the frequently encountered erythrophagocytosis by benign-appearing histiocytes, these cases resembled malignant histiocytosis. A T-cell phenotype was predicted for all four cases; however, only one case, a lymphoma with polymorphous cytologic characteristics, was of T-cell lineage. The other three cases were of B-cell lineage. The authors' results indicate that in most instances the B-cell or T-cell nature of aggressive splenic lymphomas is predictable from the distributional and cytologic features. As in lymph nodes, there are cases for which the morphologic characteristics of B-cell and T-cell lymphomas are indistinguishable.

摘要

为了确定脾脏的B细胞型和T细胞型侵袭性非霍奇金淋巴瘤之间是否存在任何一致的形态学差异,作者分析了16例累及脾脏的混合细胞型(1例)或大细胞型(15例)淋巴瘤。免疫数据来自于每例的细胞悬液或冰冻组织。5例为T细胞表型,11例为B细胞表型。支持T细胞表型的形态学特征包括上皮样组织细胞反应、淋巴瘤局限于脾脏的T区(动脉周围淋巴鞘和边缘区)以及透明细胞或多形性细胞学特征。支持B细胞表型的特征包括白髓内多个离散的结节、与小淋巴细胞淋巴瘤相关的大的融合性肿瘤结节以及大的无裂或免疫母细胞样浆细胞样细胞学特征。4例情况不寻常,因为大多数肿瘤性大细胞弥漫分布或仅在红髓中形成小聚集体,没有明确的肿瘤块或结节累及白髓。由于这种分布以及良性外观的组织细胞经常出现的红细胞吞噬现象,这些病例类似于恶性组织细胞增多症。预计这4例均为T细胞表型;然而,只有1例具有多形性细胞学特征的淋巴瘤为T细胞系。其他3例为B细胞系。作者的结果表明,在大多数情况下,侵袭性脾淋巴瘤的B细胞或T细胞性质可根据分布和细胞学特征预测。与淋巴结一样,存在B细胞和T细胞淋巴瘤的形态学特征无法区分的病例。

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