Soucy-Giguère Marie-Camille, Turgeon Pierre Yves, Sénéchal Mario
Department of Cardiology, Institut Universitaire de Cardiologie et de Pneumologie de Québec, Québec City, QC, Canada.
Int Med Case Rep J. 2019 Aug 8;12:253-259. doi: 10.2147/IMCRJ.S217568. eCollection 2019.
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.
我们报告了两名分别为22岁和31岁的年轻男性患者的病例,他们既往无病史且无心血管危险因素,因大面积前壁ST段抬高型心肌梗死(STEMI)入院。紧急冠状动脉造影显示两名患者的左前降支近端均发生急性血栓性闭塞。发现持续性血小板增多,随后的检查确诊为伴有JAK2-V617F突变阳性的原发性血小板增多症(ET)。心肌梗死作为ET的首发临床表现较为罕见,但对于无心血管危险因素且出现持续性血小板增多的患者必须予以考虑。在无危险因素的年轻患者中,STEMI的诊断可能会有很大延迟。广泛STEMI的再灌注时间延长与不良结局及心源性休克相关,这可能导致心脏移植和左心室辅助装置(LVAD)等高阶治疗。考虑到ET患者良好的长期预后,在存在严重左心室功能障碍的情况下,高阶治疗可能是一个有价值的选择。