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Acute promyelocyte leukemia arose from CALR 1 mutated post essential thrombocythemia- myelofibrosis with splanchnic vein thrombosis: A case report

机译:来自 Calr 1突变后基本血小板血症 - 骨髓血管血栓血栓形成:案例报告

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Major disease complications for patients with essential thrombocythemia (ET) include thrombosis and fibrotic or leukemic transformation. Calreticulin (CALR) mutation type 1 frequencies in ET are estimated between 7% and 11% and ET patients carryingCALRtype 1 mutation are associated with lower risk of thrombosis but higher risk of myelofibrosis transformation compared to ET patients withJAK2mutation. Leukemic transformation rates at 20 years are estimated at less than 5% for ET and risk factors for leukemic transformation are advanced age, thrombosis history, leukocytosis, and anemia. Amongst the subtypes of blast phase myeloproliferative neoplasms, acute promyelocytic leukemia is extremely rare. Herein, we present a case of a promyelocytic blast crisis of post-ET myelofibrosis with associated life-threatening splanchnic vein thrombosis. This case suggests that inflammation plays a key role in thrombotic events and fibrotic/leukemic transformation in ET patients, regardless the molecular landscape.
机译:基本血小板血症(ET)的患者的主要疾病并发症包括血栓形成和纤维化或白血病转化。钙霉素(CALR)突变型ET中的频率估计在7%至11%之间,并且携带患者的患者患者血栓形成的较低风险较低,而肌电纤维化转化的风险较高,而肌电纤维化的风险相比,与患者患者与Jak2放弃相比。对20年的白血病转型率估计不到5%,并且性白血病转型的危险因素是先进年龄,血栓形成历史,白细胞增多和贫血。在爆炸期髓系肿瘤的亚型中,急性早幼粒细胞白血病非常罕见。在此,我们提出了威胁危及危及生命的植入血管静脉血栓形成的后肌细胞爆炸危机的情况。这种情况表明,无论分子景观,炎症在患者中血栓发生和纤维化/白血病转化中的关键作用。

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