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Secondary Acute Myeloid Leukemia in a One-Year-Old Girl Diagnosed with JAK2-V617F Mutation Positive Myeloproliferative Neoplasm

机译:一岁大女孩的继发性急性髓细胞性白血病,经诊断为JAK2-V617F突变阳性骨髓增生性肿瘤

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Myeloproliferative neoplasms (MPNs) are a group of clonal disorders characterized by hyperproliferation of hematologic cell lines and have been associated with tyrosine kinase JAK2-V617F mutations. Secondary acute myeloid leukemia (sAML) is a known complication of JAK2-V617F+ MPNs and bears a poor prognosis. Although the evolution of a JAK2-V617F+ MPN to a mixed-lineage leukemia has been reported in the pediatric population, no evolutions into sAML have been described. We present a case of a one-year-old girl diagnosed with JAK2-V617F+ MPN with evolution into sAML. Despite initial morphologic remission, she eventually relapsed and succumbed to her disease.
机译:骨髓增生性肿瘤(MPN)是一组以血液细胞系过度增殖为特征的克隆性疾病,并与酪氨酸激酶JAK2-V617F突变相关。继发性急性髓细胞性白血病(sAML)是JAK2-V617F + MPN的已知并发症,预后较差。尽管在儿科人群中已经报道了JAK2-V617F + MPN向混合谱系白血病的进化,但尚未描述向sAML的进化。我们介绍了一例诊断为JAK2-V617F + MPN并演变为sAML的一岁女孩。尽管最初形态缓解,但她最终复发并屈服于疾病。

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