An interesting case of chronic myeloid leukemia with twists and turns.

IF 1.8 Q3 HEMATOLOGY
Hematology, Transfusion and Cell Therapy Pub Date : 2024-12-01 Epub Date: 2023-03-07 DOI:10.1016/j.htct.2023.02.001
Thulasi Raman Ramalingam, J Subramanian, I Nagarathinam, C Chandran, L Vaidhyanathan, J M Easow
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引用次数: 0

Abstract

Additional cytogenetic abnormalities (ACA) are known to crop up in Ph+ cells of chronic myeloid leukemia (CML) patients due to cytogenetic evolution. But the frequency of molecular evolution and ACA is much less in Ph- cells of CML patients and is poorly understood. We report an interesting and rare case of Ph+ CML, who progressed to B lymphoblastic crisis, achieved remission, and later developed Ph- acute myeloid leukemia (AML) with KMT2A gene rearrangement and no detectable BCR- ABL transcripts.

一个有趣的慢性髓性白血病病例,病情曲折。
由于细胞遗传进化,慢性髓性白血病(CML)患者的Ph+细胞中会出现额外的细胞遗传异常(ACA)。但是分子进化和ACA的频率在CML患者的Ph细胞中要少得多,而且人们对其了解甚少。我们报告了一个有趣而罕见的Ph+ CML病例,他进展到B淋巴细胞危像,获得缓解,后来发展为Ph-急性髓性白血病(AML), KMT2A基因重排,没有检测到BCR- ABL转录物。
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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来源期刊
CiteScore
2.40
自引率
4.80%
发文量
1419
审稿时长
30 weeks
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