罕见的浆细胞骨髓瘤合并双克隆伽玛病

IF 0.1 Q4 MEDICINE, GENERAL & INTERNAL
M. Mardziah, Y. Nurasyikin, T. Rafeah, N. Dian, S. A. Aziz
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引用次数: 0

摘要

已知浆细胞骨髓瘤引起免疫球蛋白(Ig)单克隆扩增,导致分泌一种独特的均质单克隆蛋白(M成分)。然而,也有报道称,它也可以导致这些单克隆M蛋白产生两个不同的克隆。虽然它相对来说非常罕见,患病率仅为所有浆细胞骨髓瘤病例的2%,但临床特征据说与单克隆γ病相似。这些双克隆伽玛病可能是由单克隆伽玛病中的一个单克隆细胞引起的,也可能是由两个不同的单克隆细胞引起的。无论疾病的机制是什么,与单克隆病例相比,对治疗的反应似乎相似,尽管一些报告显示化疗耐药。在此,我们报告一例罕见的浆细胞骨髓瘤伴IgG (lambda)和IgA (lambda)型双克隆伽玛病,其临床表现、血液学和生化指标以及对治疗的反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare occurrence of plasma cell myeloma with biclonal gammopathy
Plasma cell myeloma is known to cause expansion of a single clone of immunoglobulin (Ig) which results in the secretion of a unique homogeneous monoclonal protein (M component). However, there are cases which reported that it can also cause production of two different clones of these monoclonal M proteins. Although it is relatively very rare as the prevalence is only 2% of all plasma cell myeloma cases, the clinical features are said to be similar to monoclonal gammopathy. It is suggested that these biclonal gammopathy results from either one monoclonal cell clone in monoclonal gammopathy or two different monoclonal cell clones. Whichever the mechanism of the disease be, the response to treatment seems to be similar as compared to the monoclonal cases although some reports shows chemoresistant. Here, we report a rare case of plasma cell myeloma with IgG (lambda) and IgA (lambda) type of biclonal gammopathy, the clinical presentation, the haematological and biochemical markers as well as the response to the treatment.
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来源期刊
Medicine and Health
Medicine and Health MEDICINE, GENERAL & INTERNAL-
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