The Department of Hematopathology, UT MD Anderson Cancer Center, Houston, TX 77030, USA.
Int J Lab Hematol. 2010 Oct;32(5):461-76. doi: 10.1111/j.1751-553X.2010.01246.x. Epub 2010 Jul 7.
The fourth edition of the World Health Organization (WHO) classification of myeloid neoplasms refined the criteria for some previously described myeloid neoplasms and recognized several new entities based on recent elucidation of molecular pathogenesis, identification of new diagnostic and prognostic markers, and progress in clinical management. Protein tyrosine kinase abnormalities, including translocations or mutations involving ABL1, JAK2, MPL, KIT, PDGFRA, PDGFRB, and FGFR1, have been used as the basis for classifying myeloproliferative neoplasms (MPN). Two new entities - refractory cytopenia with unilineage dysplasia and refractory cytopenia of childhood have been added to the group of myelodysplastic syndromes (MDS), and 'refractory anemia with excess blasts-1' has been redefined to emphasize the prognostic significance of increased blasts in the peripheral blood. A list of cytogenetic abnormalities has been introduced as presumptive evidence of MDS in cases with refractory cytopenia but without morphologic evidence of dysplasia. The subgroup 'acute myeloid leukemia (AML) with recurrent genetic abnormalities' has been expanded to include more molecular genetic aberrations. The entity 'AML with multilineage dysplasia' specified in the 2001 WHO classification has been renamed 'AML with myelodysplasia-related changes' to include not only cases with significant multilineage dysplasia but also patients with a history of MDS or myelodysplasia-related cytogenetic abnormalities. The term 'therapy-related myeloid neoplasms' is used to cover the spectrum of disorders previously known as t-AML, t-MDS, or t-MDS/MPN occurring as complications of cytotoxic chemotherapy and/or radiation therapy. In this review, we summarize many of these important changes and discuss some of the diagnostic challenges that remain.
世界卫生组织(WHO)第四版髓系肿瘤分类修订了一些先前描述的髓系肿瘤的标准,并基于最近对分子发病机制的阐明、新诊断和预后标志物的识别以及临床管理的进展,确认了几种新实体。蛋白酪氨酸激酶异常,包括 ABL1、JAK2、MPL、KIT、PDGFRA、PDGFRB 和 FGFR1 的易位或突变,已被用作分类骨髓增生性肿瘤(MPN)的基础。两种新实体 - 难治性血细胞减少伴单系发育异常和儿童难治性血细胞减少症已被添加到骨髓增生异常综合征(MDS)组中,“难治性贫血伴原始细胞增多-1”已重新定义,以强调外周血中原始细胞增多的预后意义。异常核型列表已被引入,作为伴有难治性血细胞减少但无形态发育异常证据的 MDS 的假定证据。“伴有反复遗传异常的急性髓系白血病(AML)”亚组已扩大,包括更多的分子遗传学异常。在 2001 年 WHO 分类中指定的“伴多系发育异常的 AML”实体已更名为“伴伴 MDS 相关变化的 AML”,以包括不仅具有显著多系发育异常的病例,还包括具有 MDS 或 MDS 相关细胞遗传学异常病史的患者。“治疗相关髓系肿瘤”一词用于涵盖以前称为 t-AML、t-MDS 或 t-MDS/MPN 的疾病谱,这些疾病是细胞毒性化疗和/或放射治疗的并发症。在这篇综述中,我们总结了其中的许多重要变化,并讨论了一些仍然存在的诊断挑战。