Pittaluga S, Verhoef G, Criel A, Wlodarska I, Dierlamm J, Mecucci C, Van den Berghe H, De Wolf-Peeters C
Department of Pathology, K.U. Leuven, Belgium.
Am J Surg Pathol. 1996 Feb;20(2):211-23. doi: 10.1097/00000478-199602000-00010.
Only 1 to 2% of all non-Hodgkin's lymphomas (NHL) present with an enlarged spleen, most of them "small B-cell lymphomas." Recently, several reports have identified these lymphomas as marginal zone B-cell lymphomas. We reviewed 39 cases of NHL presenting with an enlarged spleen without lymphadenopathy, documented by fixed and frozen material. Two were peripheral T-cell lymphomas, four diffuse large B-cell lymphomas, and 14 hairy cell leukemias. The remaining 19 belonged to the "small B-cell" category and constitute the focus of our study. Subtyping was achieved by combining morphology, immunophenotype, and cytogenetic features according to the proposal of the International Lymphoma Study Group; in addition, analysis of the peripheral blood and bone marrow smears was performed adopting the French-American-British (FAB) criteria. From this study, we can conclude that most "small B-cell" NHL of the spleen were either mantle cell lymphomas or marginal zone cell lymphomas and, by peripheral blood analysis, that the mantle cell lymphomas corresponded to intermediate lymphocytic lymphoma and the marginal zone cell lymphomas to splenic lymphomas with villous lymphocytes. As a result, several diagnostic criteria can be proposed that may be helpful in differentiating mantle cell lymphoma from marginal zone cell lymphoma in the spleen.
所有非霍奇金淋巴瘤(NHL)中只有1%至2%会出现脾脏肿大,其中大多数为“小B细胞淋巴瘤”。最近,几份报告将这些淋巴瘤鉴定为边缘区B细胞淋巴瘤。我们回顾了39例经固定和冷冻材料记录的无淋巴结病的脾脏肿大的NHL病例。其中2例为外周T细胞淋巴瘤,4例为弥漫性大B细胞淋巴瘤,14例为毛细胞白血病。其余19例属于“小B细胞”类别,构成了我们研究的重点。根据国际淋巴瘤研究组的提议,结合形态学、免疫表型和细胞遗传学特征进行亚型分类;此外,采用法国-美国-英国(FAB)标准对外周血和骨髓涂片进行分析。从这项研究中,我们可以得出结论,脾脏的大多数“小B细胞”NHL要么是套细胞淋巴瘤,要么是边缘区细胞淋巴瘤,通过外周血分析,套细胞淋巴瘤对应于中等淋巴细胞淋巴瘤,边缘区细胞淋巴瘤对应于伴有绒毛状淋巴细胞的脾淋巴瘤。因此,可以提出一些诊断标准,可能有助于区分脾脏中的套细胞淋巴瘤和边缘区细胞淋巴瘤。