A Case of Non Secretory Type Multiple Myeloma Associated with Systemic Lupus Erythematosus

Y. Jeong, H. S. Kim, Eun Jeong Kim, Yunsuek Kim, Chiyoung Park, B. Shin, G. Park
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引用次数: 1

Abstract

The development of malignant tumors is a more frequent finding in lupus patients than the general population. However, the incidence of multiple myeloma associated with systemic lupus erythematosus (SLE) is a rare manifestation. SLE is an autoimmune disease characterized by B cell hyperactivity, formation of autoantibodies, and multi-clonal hypergammaglobulinemia. Serum immunoglobulin increases, with a specific increase in IgG, which is due to an increase in autoantibody formation related to extrinsic and intrinsic antigens. We report on a patient with SLE combined with IgG, lambda type nonsecretory multiple myeloma, which was diagnosed with refractory anemia and hypergammaglobulinemia.
非分泌型多发性骨髓瘤合并系统性红斑狼疮1例
恶性肿瘤的发展是一个更常见的发现狼疮患者比一般人群。然而,多发性骨髓瘤与系统性红斑狼疮(SLE)的发病率是一种罕见的表现。SLE是一种自身免疫性疾病,以B细胞过度活跃、自身抗体形成和多克隆高γ球蛋白血症为特征。血清免疫球蛋白增加,IgG特异性增加,这是由于与外在和内在抗原相关的自身抗体形成增加。我们报告一例SLE合并IgG, lambda型非分泌性多发性骨髓瘤,诊断为难治性贫血和高γ球蛋白血症。
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