骨髓增生异常综合征和急性髓系白血病的诊断谱。

IF 5.1 2区 医学 Q1 PATHOLOGY
Daniel A Arber, Attilio Orazi
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引用次数: 0

摘要

骨髓增生异常综合征(MDS)和急性髓性白血病(AML)的国际共识分类(ICC)扩展了先前分类的工作,以完善MDS和AML的诊断标准,并确定特定的遗传疾病亚型。本文综述了从ICC角度诊断MDS和AML的方法。对于MDS,检测SF3B1突变(通常与环状铁母细胞相关)的意义以及TP53突变的不良预后现在被纳入考虑。对于AML,包括了新的遗传类别,并且通过识别具有TP53突变的AML和具有先前治疗或MDS相关基因突变的AML,现在的分类纳入了额外的临床显著基因突变。最后,引入了新的MDS/AML类别,用于无复发性新生遗传异常的成人患者,其外周血或骨髓母细胞含量为10%至19%,根据临床结果允许更大的治疗灵活性。虽然遗传类别的增加和胚细胞需求的变化可能令人困惑,但提供了一种循序渐进的方法,以便易于使用分类。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Diagnostic Spectrum of Myelodysplastic Syndromes and Acute Myeloid Leukemia.

The International Consensus Classification (ICC) of myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML) expands on the work of prior classifications to refine the diagnostic criteria for MDS and AML and to identify specific genetic disease subtypes. This review summarizes the approach to the diagnosis of MDS and AML from the ICC perspective. For MDS, the significance of detecting mutations in SF3B1, usually associated with ring sideroblasts, as well as the poor prognosis of mutations of TP53 are now included. For AML, new genetic categories are included, and the classification now incorporates additional clinically significant gene mutations by recognizing AML with TP53 mutation and AML with mutations in genes associated with prior therapy or MDS. Finally, the new category of MDS/AML is introduced for adult patients without recurrent de novo genetic abnormalities with 10% to 19% peripheral blood or bone marrow blasts that allow for more treatment flexibility based on clinical findings. While the increase in genetic categories and changes in blast cell requirements can be confusing, a stepwise approach is provided to allow easy use of the classification.

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来源期刊
CiteScore
10.30
自引率
3.00%
发文量
88
审稿时长
>12 weeks
期刊介绍: Advances in Anatomic Pathology provides targeted coverage of the key developments in anatomic and surgical pathology. It covers subjects ranging from basic morphology to the most advanced molecular biology techniques. The journal selects and efficiently communicates the most important information from recent world literature and offers invaluable assistance in managing the increasing flow of information in pathology.
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