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源于单克隆起源的浆细胞样淋巴瘤患者中的三克隆丙种球蛋白病(IgA κ、IgG κ和IgM κ)

Triclonal gammopathy (IgA kappa, IgG kappa, and IgM kappa) in a patient with plasmacytoid lymphoma derived from a monoclonal origin.

作者信息

Murata T, Fujita H, Harano H, Hukawa M, Kanamori H, Matsuzaki M, Mohri H, Kudoh J, Shimizu N, Okubo T

机构信息

First Department of Internal Medicine, Yokohama City University, Japan.

出版信息

Am J Hematol. 1993 Feb;42(2):212-6. doi: 10.1002/ajh.2830420213.

Abstract

We report the case of a 64-year-old woman with plasma cytoid lymphoma of the ileum and gastric wall. Serum protein electrophoresis and immunoelectrophoresis showed a triclonal IgG kappa, IgA kappa, and IgM kappa gammopathy. Biopsy of the tumor revealed three different cell types, which were stained with antibodies specific for IgG, IgA, and IgM. However, DNA analysis of immunoglobulin gene rearrangements using JH, C mu, and C kappa gene probes showed a monoclonal pattern. These results suggest that the three types of malignant cells producing different classes of immunoglobulins were derived from a single clone of B-cells that had undergone a "class switch".

摘要

我们报告了一例64岁女性患有回肠和胃壁浆细胞样淋巴瘤的病例。血清蛋白电泳和免疫电泳显示为三克隆性IgG κ、IgA κ和IgM κ丙种球蛋白病。肿瘤活检显示三种不同的细胞类型,分别用针对IgG、IgA和IgM的特异性抗体染色。然而,使用JH、Cμ和Cκ基因探针进行免疫球蛋白基因重排的DNA分析显示为单克隆模式。这些结果表明,产生不同类免疫球蛋白的三种恶性细胞源自经历了“类别转换”的单个B细胞克隆。

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