Suppr超能文献

非系统性轻链淀粉样变相关性单克隆丙种球蛋白病肾损害中的细胞遗传学异常:一个有待探索的领域。

Cytogenetic abnormality in non-systemic light chain amyloidosis monoclonal gammopathy of renal significance: A field needs to be explored.

机构信息

National Clinical Research Center of Kidney Diseases, Jinling Hospital, Nanjing University School of Medicine, Nanjing, China.

出版信息

Br J Haematol. 2024 Nov;205(5):1677-1678. doi: 10.1111/bjh.19768. Epub 2024 Sep 18.

Abstract

The role of cytogenetic abnormalities in non-systemic light chain amyloidosis monoclonal gammopathy of renal significance diseases still needs to be clarified. Bhutani et al. present the results of a study investigating the underlying plasma cell cytogenetic abnormalities in monoclonal immunoglobulin deposition disease (MIDD). The results show that translocation (11;14) is a common abnormality in MIDD and affects the presentation and outcomes. Commentary on: Bhutani et al. Translocation (11;14) is a common cytogenetic abnormality in clonal plasma cells in monoclonal immunoglobulin deposition disease. Br J Haematol 2024; 205:1860-1865.

摘要

在非系统性轻链淀粉样变性单克隆丙种球蛋白相关性肾脏疾病中,细胞遗传学异常的作用仍需阐明。Bhutani 等人报告了一项研究的结果,该研究调查了单克隆免疫球蛋白沉积病(MIDD)中浆细胞细胞遗传学异常的潜在情况。结果表明,易位(11;14)是 MIDD 的常见异常,会影响其表现和结局。述评:Bhutani 等人。易位(11;14)是单克隆免疫球蛋白沉积病克隆浆细胞中的常见细胞遗传学异常。英国血液学杂志 2024;205:1860-1865。

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