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What cardiologists should know about essential thrombocythemia and acute myocardial infarction: report of two cases and advanced heart failure therapies considerations

机译:心脏病专家应了解哪些有关原发性血小板增多症和急性心肌梗塞的报道:2例病例报告和高级心力衰竭治疗注意事项

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We present the cases of two young male patients aged 22 and 31 without prior medical history nor cardiovascular risk factors, who presented to the hospital with large anterior ST-elevation myocardial infarction (STEMI). Urgent coronary angiography revealed acute thrombotic occlusion of the proximal left anterior descending artery in both patients. Persistent thrombocytosis was noted and subsequent investigations led to the diagnosis of essential thrombocythemia (ET) with positive JAK2-V617F mutation. Myocardial infarction as a first clinical manifestation of ET is rare but must be considered in patients without cardiovascular risk factors who show persistent thrombocytosis. In young patients without risk factors, there may be great delays before the diagnosis of STEMI is made. Longer time to revascularization of extensive STEMI is associated with adverse outcomes and cardiogenic shock which can lead to advanced therapies like heart transplant and left ventricular assist device (LVAD). Considering the favorable long-term prognosis of patients with ET, advanced therapies may be a valuable option in the presence of severe left ventricular dysfunction.
机译:我们介绍了两名既往没有既往病史或心血管危险因素的22岁和31岁的年轻男性患者,他们因巨大的前ST抬高型心肌梗死(STEMI)被送往医院。紧急冠状动脉造影显示两名患者的左前降支动脉近端均发生急性血栓闭塞。注意到持续性血小板增多症,随后的研究导致诊断为JAK2-V617F阳性突变的原发性血小板增多症(ET)。心肌梗塞作为ET的首例临床表现很少见,但对于没有心血管危险因素且持续存在血小板增多症的患者,必须考虑将其作为考虑因素。在没有危险因素的年轻患者中,STEMI诊断之前可能会有很大的延迟。广泛的STEMI血运重建时间较长与不良结局和心源性休克有关,可导致先进的疗法,例如心脏移植和左心室辅助装置(LVAD)。考虑到ET患者的长期预后良好,在存在严重的左心功能不全的情况下,先进的治疗可能是有价值的选择。

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