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接受新型靶向异柠檬酸脱氢酶1/2抑制剂治疗的急性髓系白血病患者的骨髓特征

Bone Marrow Features in Patients With Acute Myeloid Leukemia Treated With Novel Targeted Isocitrate Dehydrogenase 1/2 Inhibitors.

作者信息

Hagiya Ashley, Vaidya Poorva, Khedro Tarek, Yaghmour Bassam, Siddiqi Imran, Yaghmour George

机构信息

Department of Pathology, Keck School of Medicine of University of Southern California, Los Angeles, CA 90033, USA.

Internal Medicine, Keck School of Medicine of University of Southern California, Los Angeles, CA 90033, USA.

出版信息

World J Oncol. 2019 Dec;10(6):226-230. doi: 10.14740/wjon1231. Epub 2019 Dec 16.

DOI:10.14740/wjon1231
PMID:31921378
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6940036/
Abstract

This case report aimed to review the bone marrow features of patients with acute myeloid leukemia (AML) treated with isocitrate dehydrogenase 1/2 () inhibitors. Five patients with AML treated with an inhibitor were identified and retrospectively reviewed. We described the morphologic and immunophenotypic findings in the bone marrow, as well as ancillary study results. Two patients showed a hypercellular bone marrow with morphologic and immunophenotypic differentiation of blasts. The bone marrow of one patient displayed a hypoplastic phase. Four of the five patients demonstrated unusual morphologic and/or immunophenotypic populations, including basophilia with mild alterations on the myeloid blasts, a small subset of blasts with expression of T-cell markers not seen in the original immunophenotype, a cluster of differentiation 117 (CD117)-positive progenitor population with erythroid differentiation, and another population reminiscent of erythroid differentiation. Unusual morphologic and immunophenotypic populations can be seen in the bone marrows of patients treated with inhibitors in the presence or absence of definite residual disease. The significance of these populations is uncertain, but further studies could be helpful to understand the meaning of these findings.

摘要

本病例报告旨在回顾接受异柠檬酸脱氢酶1/2(IDH1/2)抑制剂治疗的急性髓系白血病(AML)患者的骨髓特征。确定了5例接受IDH1/2抑制剂治疗的AML患者,并进行回顾性分析。我们描述了骨髓的形态学和免疫表型结果,以及辅助检查结果。2例患者骨髓细胞增多,原始细胞有形态学和免疫表型分化。1例患者的骨髓显示增生低下期。5例患者中有4例表现出异常的形态学和/或免疫表型细胞群,包括嗜碱性粒细胞增多伴髓系原始细胞轻度改变、一小部分原始细胞表达原始免疫表型中未见到的T细胞标志物、一群分化簇117(CD117)阳性且有红系分化的祖细胞群,以及另一群类似红系分化的细胞群。在接受IDH1/2抑制剂治疗的患者骨髓中,无论有无明确的残留病,均可出现异常的形态学和免疫表型细胞群。这些细胞群的意义尚不确定,但进一步研究可能有助于理解这些发现的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3b9/6940036/19ccf5473190/wjon-10-06-226-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3b9/6940036/19ccf5473190/wjon-10-06-226-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3b9/6940036/19ccf5473190/wjon-10-06-226-g001.jpg

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