骨髓增殖性疾病背景下慢性骨髓性白血病的出现:JAK2V617F是BCR-ABL易位的潜在危险因素

Sai Ravi Kiran Pingali , Michelle A. Mathiason , Steven D. Lovrich , Ronald S. Go
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引用次数: 35

摘要

我们报道了一名患有jak2v617f阳性真性红细胞增多症的患者在接受15年的静脉切开术后出现慢性髓性白血病(CML)。真性红细胞增多症的临床和分子表现在CML诊断时受到抑制,仅在用伊马替尼成功治疗白血病后才再次出现。在当前文献的背景下,我们探索了骨髓增生性疾病和CML之间的潜在关联,并基于每种特定情况的已知流行病学数据发现了高于预期的巧合。我们假设骨髓增生性疾病(JAK2V617F或导致JAK2V617F的分子事件)是CML (BCR-ABL易位)的危险因素。由于治疗的意义,临床医生应该意识到,这些情况共同发生的频率比以前认为的要高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Emergence of Chronic Myelogenous Leukemia From a Background of Myeloproliferative Disorder: JAK2V617F as a Potential Risk Factor for BCR-ABL Translocation

We report the emergence of chronic myelogenous leukemia (CML) in a patient with JAK2V617F-positive polycythemia vera after 15 years of phlebotomy. The polycythemia vera clinical and molecular findings were suppressed at the time of CML diagnosis, only to re-emerge after the leukemia was successfully treated with imatinib. We explored the potential association between myeloproliferative disorders and CML in the context of the current literature and found a higher-than-expected coincidence based on known epidemiologic data for each specific condition. We hypothesize that myeloproliferative disorder (JAK2V617F or molecular events that cause JAK2V617F) is a risk factor for CML (BCR-ABL translocation). Because of therapeutic implications, clinicians should be aware that the conditions co-occur more frequently than once thought.

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