Okabe Hiroki, Sonoda Shinjo, Abe Koji, Doi Hideki, Matsumura Toshiyuki, Otsuji Yutaka
The Second Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyusyu, Japan.
Department of Cardiology, Kumamoto Rousai Hospital, Kumamoto, Japan.
J Cardiol Cases. 2019 Jun 24;20(4):111-114. doi: 10.1016/j.jccase.2019.06.001. eCollection 2019 Oct.
A 59-year-old female was brought to our emergency room with severe chest pain. Based on the electrocardiogram (ECG) and echocardiography, an acute coronary syndrome (ACS) was suspected. Her initial ECG showed ST elevation in the inferior leads (II, III, and aVF), which had progressed to involve the anterior leads (V2-V4) by the time she was shifted to the catheterization room. A coronary angiogram revealed total occlusion of the mid-left anterior descending (LAD) artery and a filling defect of the distal right coronary artery. Although we had emergently treated her using thrombus aspiration following stent implantation, lots of thrombi re-formed on the stent. We surmised her ACS was primarily caused by thrombus formation due to polycythemia vera (PV) based on the presence of increased blood consistency on admission. We performed repetitive long-inflation using a perfusion balloon and repeated thrombus aspiration. Finally, she was diagnosed as an untreated case of PV as a result of detailed blood investigations. Thereafter, we successfully treated her using the combination of dual antiplatelet therapy and direct oral anticoagulant therapy. Our experience highlights the importance of an urgent identification of PV. Effective management strategies should be successfully implemented in such patients as soon as possible. < Polycythemia vera (PV) is an idiopathic, chronic myeloproliferative disease characterized by an increased red blood cell count and hematocrit, which in turn causes systematic thrombosis. A resultant acute myocardial infarction is therefore complicated and difficult to manage, due to the patient's continuous hypercoagulable state. In the absence of a defined treatment approach, newer and successfully implemented strategies for the management of consequent thrombotic events in PV patients are indispensable to clinicians.>.
一名59岁女性因严重胸痛被送至我院急诊室。根据心电图(ECG)和超声心动图检查,怀疑为急性冠状动脉综合征(ACS)。她最初的心电图显示下壁导联(II、III和aVF)ST段抬高,在转至导管室时已进展至累及前壁导联(V2-V4)。冠状动脉造影显示左前降支(LAD)中段完全闭塞,右冠状动脉远端有充盈缺损。尽管我们在支架植入后紧急对她进行了血栓抽吸治疗,但支架上仍有大量血栓重新形成。基于入院时血液黏稠度增加,我们推测她的ACS主要是由真性红细胞增多症(PV)导致的血栓形成引起的。我们使用灌注球囊进行了反复长时间扩张,并重复进行血栓抽吸。最终,通过详细的血液检查,她被诊断为未经治疗的PV病例。此后,我们使用双联抗血小板治疗和直接口服抗凝治疗联合成功地对她进行了治疗。我们的经验强调了紧急识别PV的重要性。应尽快在此类患者中成功实施有效的管理策略。<真性红细胞增多症(PV)是一种特发性慢性骨髓增殖性疾病,其特征是红细胞计数和血细胞比容增加,进而导致系统性血栓形成。因此,由于患者持续处于高凝状态,由此导致的急性心肌梗死病情复杂且难以处理。在缺乏明确治疗方法的情况下,针对PV患者后续血栓事件管理的更新且成功实施的策略对临床医生来说必不可少。>