[细胞遗传学检测在恶性血液病诊断中的作用]。

Magyar onkologia Pub Date : 2024-12-10 Epub Date: 2024-11-06
Anikó Ujfalusi
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引用次数: 0

摘要

在恶性血液病中,染色体畸变和基因突变等克隆基因改变是导致异常造血细胞失控分裂的原因。克隆变异的检测不仅具有诊断意义,还具有预后和治疗意义。通过检测克隆变异,可以对患者进行基于风险的差异化治疗,并使用靶向(基因型特异性)疗法。染色体异常可通过细胞基因组检测(核型分析、荧光原位杂交--FISH、芯片)来确定。对于慢性髓性白血病、骨髓增生异常性肿瘤和急性白血病,染色体分析是诊断时必须进行的检测。在某些淋巴恶性肿瘤(慢性淋巴细胞白血病、多发性骨髓瘤)中,可通过 FISH 方法检测亚显微异常和易位,而不是核型分析。尽管高灵敏度的新一代测序技术迅速普及,细胞遗传学研究在恶性血液病的常规诊断中仍然必不可少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The role of cytogenetic tests in the diagnosis of malignant hematologic diseases].

In malignant hematological diseases, clonal genetic alterations, such as chromosomal aberrations and gene mutations, are responsible for the uncontrolled division of abnormal hemopoietic cells. The detection of clonal variants has not only diagnostic, but also prognostic and therapeutic significance. They enable risk-based differentiated treatment of patients and the use of targeted (genotype-specific) therapies. Chromosomal abnormalities can be identified with cytogenomic testing (karyotyping, fluorescent in situ hybridization - FISH, microarray). In chronic myeloid leukemia, myelodysplastic neoplasia and acute leukemias, chromosome analysis is a mandatory test at the time of diagnosis. In some lymphoid malignancies (chronic lymphocytic leukemia, multiple myeloma), instead of karyotyping, submicroscopic abnormalities and translocations are detected by FISH method. Despite the rapid spread of high-sensitivity new-generation sequencing techniques, cytogenetic studies are still essential in the routine diagnosis of malignant hematological diseases.

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