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原发性胃肠道B细胞淋巴瘤的组织形态学和免疫表型谱

Histomorphologic and immunophenotypic spectrum of primary gastro-intestinal B-cell lymphomas.

作者信息

Mielke B, Möller P

机构信息

Institute of Pathology, Univesity of Heidelberg, Germany.

出版信息

Int J Cancer. 1991 Feb 1;47(3):334-43. doi: 10.1002/ijc.2910470304.

DOI:10.1002/ijc.2910470304
PMID:1704353
Abstract

In order to compare primary gastro-intestinal (GI) B-cell lymphomas histomorphologically and immunophenotypically with orthologous steps of B-cell differentiation within the mucosa-associated lymphoid tissue (MALT) of the GI tract, a comprehensive panel of well characterized leucocyte differentiation antigens was composed. It comprised immunoglobulin constituents CD5, CD10, CD11c, CD20, CD23, CD24, CD30, CDw32, CD38, CD39, CDw75, CD76, and vimentin. These antigens yield characteristic immunoprofiles for the following B-cell compartments of the MALT, per se closely linked to cytologically distinct B-cell phenotypes: mantle zone (MZ), extrafollicular compartment (EF), follicle center (FC), and plasma-cell compartment (PC). An unselected series of 31 MALT B lymphomas (13 of low and 18 of high grade malignancy) was classified histologically in routine preparations and subsequently characterized immunohistochemically using fresh frozen tissue, monoclonal antibodies (MAbs) against the antigen panel listed above, and an indirect immunoperoxidase method. The final classification considered both morphology and immunoprofile of tumor cells. Ten tumors were "typical" in both respects: 2 closely corresponded to MZ, 5 to EF, 2 to FC and 1 to PC. The remaining 21 cases were characterized as "atypical" because of anaplastic cytology and/or abnormal co-expression and/or loss of antigens. A hybrid EF/FC phenotype was most frequently observed together with centrocyte-like or centrocytic anaplastic cytology of tumor cells. We conclude that MALT B-cell neoplasia comprises a broad spectrum of histo- and immunophenotypes ranging from well differentiated forms closely mimicking normal B-cell development to highly abnormal tumors which cannot be subclassified.

摘要

为了从组织形态学和免疫表型上比较原发性胃肠道(GI)B细胞淋巴瘤与胃肠道黏膜相关淋巴组织(MALT)内B细胞分化的同源步骤,构建了一组全面的、特征明确的白细胞分化抗原。它包括免疫球蛋白成分CD5、CD10、CD11c、CD20、CD23、CD24、CD30、CDw32、CD38、CD39、CDw75、CD76以及波形蛋白。这些抗原为MALT的以下B细胞区室产生特征性免疫谱,这些区室本身与细胞学上不同的B细胞表型密切相关:套区(MZ)、滤泡外区室(EF)、滤泡中心(FC)和浆细胞区室(PC)。对一组未经选择的31例MALT B淋巴瘤(13例低级别和18例高级别恶性肿瘤)在常规切片中进行组织学分类,随后使用新鲜冷冻组织、针对上述抗原组的单克隆抗体(MAb)以及间接免疫过氧化物酶法进行免疫组织化学特征分析。最终分类考虑肿瘤细胞的形态和免疫谱。10例肿瘤在两方面均为“典型”:2例与MZ密切对应,5例与EF对应,2例与FC对应,1例与PC对应。其余21例因肿瘤细胞的间变细胞学和/或异常共表达和/或抗原缺失而被表征为“非典型”。最常观察到的是EF/FC混合表型,同时伴有肿瘤细胞的中心细胞样或中心细胞间变细胞学。我们得出结论,MALT B细胞肿瘤形成包括广泛的组织学和免疫表型谱,从紧密模仿正常B细胞发育的高分化形式到无法进行亚分类的高度异常肿瘤。

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