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

被引:0
|
作者
Li, Ke [1 ]
Johnson, Rebecca L. [1 ]
Li, Shiyong [2 ]
Thorson, John A. [1 ]
Mulroney, Carolyn M. [3 ]
Dell'Aquila, Marie L. [1 ]
Wang, Huan-You [1 ]
机构
[1] Univ Calif San Diego Hlth Syst, Dept Pathol, La Jolla, CA 92093 USA
[2] Emory Univ, Dept Pathol, Atlanta, GA 30322 USA
[3] Univ Calif San Diego Hlth Syst, Dept Med, Div Hematol, La Jolla, CA 92093 USA
关键词
t(14; 22)(q32; q11); K-deleting element; marginal zone B-cell lymphoma; systemic lupus erythematosus; NON-HODGKIN-LYMPHOMA; LYMPHOPROLIFERATIVE DISORDERS; MALIGNANCIES; EXPRESSION; REMISSION; LEUKEMIA; THERAPY; GENES;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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.
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页码:5221 / 5231
页数:11
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