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首页> 外文期刊>International Journal of Clinical and Experimental Pathology >Nodal involvement by marginal zone B-cell lymphoma harboring t(14;22)(q32;q11) involving immunoglobulin heavy chain and light chain lambda as the sole karyotypically recognizable abnormality in a patient with systemic lupus erythematosus
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Nodal involvement by marginal zone B-cell lymphoma harboring t(14;22)(q32;q11) involving immunoglobulin heavy chain and light chain lambda as the sole karyotypically recognizable abnormality in a patient with systemic lupus erythematosus

机译:系统性红斑狼疮患者的边缘区B细胞淋巴瘤累及t(14; 22)(q32; q11),涉及免疫球蛋白重链和轻链λ作为唯一的核型识别异常

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摘要

Recurrent non-random balanced chromosomal translocation, usually involving the immunoglobulin heavy chain (IgH) gene or an immunoglobulin light chain gene and a proto-oncogene, which results in the overexpression of the latter under the control of an enhancer or promoter of the former, is a hallmark of many types of non-Hodgkin lymphoma (NHL) of B-cell origin. However, translocations between IgH and the immunoglobulin (Ig) light chain lambda gene (IgL), namely, a t(14;22)(q32;q11), have rarely been described in B-cell NHL. Herein we report the first case of marginal zone B-cell lymphoma harboring a t(14;22)(q32;q11) as its sole genetic abnormality in a patient with a 12-year history of systemic lupus erythematosus (SLE). Other interesting findings of this case include: 1) the neoplastic B-cells lack expression of both surface and cytoplasmic Ig light chain as revealed by flow cytometry and 2) monoclonal rearrangement of Ig light chain kappa (IgK) only due to k-deleting element (kde) recombination event. This case illustrates the necessity of utilizing a multi-modality approach in the diagnosis of B-cell NHL.
机译:反复发生的非随机平衡染色体易位,通常涉及免疫球蛋白重链(IgH)基因或免疫球蛋白轻链基因和原癌基因,导致后者在前者的增强子或启动子的控制下过表达,是许多类型的B细胞源性非霍奇金淋巴瘤(NHL)的标志。但是,在B细胞NHL中很少描述IgH和免疫球蛋白(Ig)轻链λ基因(IgL)之间的易位,即t(14; 22)(q32; q11)。在此,我们报道了第一例以t(14; 22)(q32; q11)为特征的边缘性B细胞淋巴瘤,这是系统性红斑狼疮(SLE)有12年病史的患者的唯一遗传异常。该病例的其他有趣发现包括:1)肿瘤B细胞缺乏流式细胞仪显示的表面和细胞质Ig轻链的表达,以及2)仅由于k缺失元件导致的Ig轻链κ(IgK)的单克隆重排(kde)重组事件。这种情况说明了在B细胞NHL诊断中采用多模式方法的必要性。

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