Suppr超能文献

对4例B细胞慢性淋巴细胞白血病或淋巴浆细胞样淋巴瘤(里氏综合征)患者随后发生的继发性弥漫性大B细胞淋巴瘤的免疫球蛋白重链基因分析。

Analysis of the immunoglobulin heavy chain gene of secondary diffuse large B-cell lymphoma that subsequently developed in four cases with B-cell chronic lymphocytic leukemia or lymphoplasmacytoid lymphoma (Richter syndrome).

作者信息

Nakamura N, Kuze T, Hashimoto Y, Hoshi S, Tominaga K, Sasaki Y, Shirakawa A, Sato M, Maeda K, Abe M

机构信息

Department of Pathology, Fukushima Medical University School of Medicine, Fukushima, Japan.

出版信息

Pathol Int. 2000 Aug;50(8):636-43. doi: 10.1046/j.1440-1827.2000.01094.x.

Abstract

The immunoglobulin heavy chain gene (IgH gene) was analysed in four cases of B-cell Richter syndrome, in order to determine whether a secondary diffuse large B-cell lymphoma (DLBCL) could arise from the same clone as the initial B-cell chronic lymphocytic leukemia (B-CLL) and lymphoplasmacytoid lymphoma (LPL) or be a de novo event, and whether secondary DLBCL shows an intraclonal microheterogeneity. Both the initial B-CLL and secondary DLBCL in two cases expressed CD5 antigen. Both samples of the initial B-CLL or LPL and the secondary DLBCL in three cases were examined for comparison. The polymerase chain reaction-amplified IgH gene of secondary DLBCL in two cases (CD5+ case and CD5- case) were different from those of the initial B-CLL, revealing a new malignant clone. The other case (CD5-) showed that secondary DLBCL had a sequence identical to the initial LPL, indicating the same clonal origin. The variable region of the IgH gene of secondary DLBCL (CD5+ two cases and CD5- two cases) exhibited a 0.5-9.0% somatic mutation range and no intraclonal microheterogeneity.

摘要

为了确定继发性弥漫性大B细胞淋巴瘤(DLBCL)是否可能源自与初始B细胞慢性淋巴细胞白血病(B-CLL)和淋巴浆细胞样淋巴瘤(LPL)相同的克隆,或者是一个新发事件,以及继发性DLBCL是否表现出克隆内微异质性,我们对4例B细胞Richter综合征患者的免疫球蛋白重链基因(IgH基因)进行了分析。2例患者的初始B-CLL和继发性DLBCL均表达CD5抗原。为了进行比较,对3例患者的初始B-CLL或LPL样本以及继发性DLBCL样本都进行了检测。2例继发性DLBCL(CD5阳性病例和CD5阴性病例)的聚合酶链反应扩增的IgH基因与初始B-CLL的不同,显示出一个新的恶性克隆。另一例(CD5阴性)显示继发性DLBCL的序列与初始LPL相同,表明克隆起源相同。继发性DLBCL(2例CD5阳性和2例CD5阴性)的IgH基因可变区表现出0.5%-9.0%的体细胞突变范围,且无克隆内微异质性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验