Myelodysplastic Syndrome with Excess Blasts 2 (MDS-EB-2): A Historical Overview and Review of Forthcoming Classifications.

Julian S Tan, Juli-Anne Gardner, Katherine A Devitt, Joanna L Conant
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Abstract

Objectives: Myelodysplastic syndrome with excess blasts-2 (MDS-EB-2) primarily affects adults older than 50 years and confers a worse prognosis with a higher risk of transformation to acute myeloid leukemia (AML) compared to myelodysplastic syndrome (MDS) and MDS with excess blasts-1 (MDS-EB-1). In ordering diagnostic studies for MDS, cytogenetic and genomic studies are vital as they have significant clinical and prognostic implications for the patient. We present a case of a 71-year-old male diagnosed with MDS-EB-2 with a pathogenic loss-of-function TP53 variant and discuss presentation, pathogenesis, and the importance of thorough diagnostic testing through multiple modalities to accurately diagnose and subtype MDS. In addition, we explore a historical overview of the diagnostic criteria of MDS-EB-2 and how it has changed over time from the World Health Organization (WHO) 4th edition in 2008, the WHO revised 4th edition in 2017, and the upcoming WHO 5th edition and International Consensus Classification (ICC) for 2022.

骨髓增生异常综合征伴过多母细胞2 (MDS-EB-2):历史回顾和即将到来的分类回顾。
目的:骨髓增生异常综合征伴过量母细胞-2 (MDS- eb -2)主要影响50岁以上的成年人,与骨髓增生异常综合征(MDS)和MDS伴过量母细胞-1 (MDS- eb -1)相比,预后更差,转化为急性髓性白血病(AML)的风险更高。在为MDS安排诊断研究时,细胞遗传学和基因组学研究至关重要,因为它们对患者具有重要的临床和预后意义。我们报告一例71岁男性被诊断为MDS- eb -2伴致病性功能丧失TP53变异的病例,并讨论其表现、发病机制以及通过多种方式进行全面诊断测试以准确诊断和分型MDS的重要性。此外,我们还探讨了MDS-EB-2诊断标准的历史概况,以及它是如何随着时间的推移而变化的,从2008年世界卫生组织(WHO)第4版,到2017年世卫组织修订的第4版,以及即将到来的世卫组织第5版和国际共识分类(ICC) 2022年。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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