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A Case of Myeloid Sarcoma with Correlation to JAK2V617F Mutation, Complicated by Myelofibrosis and Secondary Acute Myeloid Leukemia

机译:一例与JAK2V617F突变相关的髓样肉瘤,并发骨髓纤维化和继发性急性髓样白血病

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The activating mutation of JAK2, V617F, has been found as a frequent mutation in myeloproliferative neoplasms (MPNs), including polycythemia vera (PV), essential thrombocytosis (ET), and primary myelofibrosis (PMF). This mutation is observed not only in MPNs, but also in chronic myelomonocytic leukemia, myelodysplastic syndrome and acute myeloid leukemia (AML). We report a case of myeloid sarcoma and myelofibrosis, followed by secondary AML, with detection of homozygous JAK2 V617F mutation. This report describes the first case of myeloid sarcoma with JAK2 V617F mutation and implication of its progression to AML.
机译:JAK2的激活突变V617F已被发现是骨髓增生性肿瘤(MPN)的常见突变,包括真性红细胞增多症(PV),原发性血小板增多症(ET)和原发性骨髓纤维化(PMF)。这种突变不仅在MPN中观察到,而且在慢性粒细胞单核细胞白血病,骨髓增生异常综合症和急性髓细胞性白血病(AML)中也观察到。我们报告一例髓样肉瘤和骨髓纤维化,继发继发性AML,并检测出纯合JAK2 V617F突变。该报告描述了首例具有JAK2 V617F突变的髓样肉瘤及其向AML发展的意义。

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