Morsia E, Goteri G, Torre E, Garvey K B, Discepoli G, Tassoni A, Mancini S, Giantomassi F, Poloni A, Olivieri A, Rupoli S
Clinica Ematologica, Ospedali Riuniti di Ancona, Ancona, Italy.
Anatomia Patologica, Ospedali Riuniti di Ancona, Ancona, Italy.
Leuk Res Rep. 2021 May 8;15:100243. doi: 10.1016/j.lrr.2021.100243. eCollection 2021.
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 carrying type 1 mutation are associated with lower risk of thrombosis but higher risk of myelofibrosis transformation compared to ET patients with mutation. 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.
原发性血小板增多症(ET)患者的主要疾病并发症包括血栓形成以及纤维化或白血病转化。ET患者中1型钙网蛋白(CALR)突变频率估计在7%至11%之间,与携带其他突变的ET患者相比,携带1型突变的ET患者血栓形成风险较低,但骨髓纤维化转化风险较高。ET患者20年白血病转化率估计低于5%,白血病转化的风险因素包括高龄、血栓形成史、白细胞增多和贫血。在急变期骨髓增殖性肿瘤的亚型中,急性早幼粒细胞白血病极为罕见。在此,我们报告一例ET后骨髓纤维化的早幼粒细胞急变期病例,伴有危及生命的内脏静脉血栓形成。该病例表明,无论分子背景如何,炎症在ET患者的血栓形成事件以及纤维化/白血病转化中起关键作用。