Suppr超能文献

骨髓增生异常综合征的克隆性研究:通过荧光原位杂交检测骨髓细胞涂片中的8号染色体三体

Study of clonality in myelodysplastic syndromes: detection of trisomy 8 in bone marrow cell smears by fluorescence in situ hybridization.

作者信息

Abruzzese E, Buss D, Rainer R, Rao P N, Pettenati M J

机构信息

Department of Pediatrics, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, NC 27157-1076, USA.

出版信息

Leuk Res. 1996 Jul;20(7):551-7. doi: 10.1016/0145-2126(95)00130-1.

Abstract

The lineage involvement in myelodysplastic syndromes (MDS) is still unclear. To determine the clonality and the evolution of the disorder, a retrospective study on bone marrow smears from seven MDS patients with trisomy 8 was performed using fluorescence in situ hybridization (FISH). We observed that the trisomy of chromosome 8 was selectively expressed in the myeloid-derived cells. No mature lymphocytes or plasma cells expressed three signals. Our studies demonstrate here the value of FISH for identifying the affected cell lineage. Furthermore, the easy quantification of the abnormal cells can help in assessing the progression of the disease.

摘要

骨髓增生异常综合征(MDS)中的谱系受累情况仍不明确。为了确定该疾病的克隆性及演变,我们使用荧光原位杂交(FISH)技术对7例8号染色体三体的MDS患者的骨髓涂片进行了回顾性研究。我们观察到8号染色体三体在髓系来源的细胞中选择性表达。未发现成熟淋巴细胞或浆细胞表达三个信号。我们的研究在此证明了FISH在识别受累细胞谱系方面的价值。此外,对异常细胞的轻松定量有助于评估疾病的进展。

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