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Updated: Dec 30, 2025

Myocardial Infarction and Functional Outcome Assessment in Pigs
Published on: April 25, 2014
Acute myocardial infarction following sequential multi-vessel occlusion in a case of polycythemia vera
Hiroki Okabe1, Shinjo Sonoda1, Koji Abe2
1The Second Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyusyu, Japan.
Insights
This case study shows that polycythemia vera (PV) can cause acute coronary syndrome (ACS) due to thrombosis. Early identification and management of PV are crucial for treating these complex cardiac events.
Area of Science:
- Cardiology
- Hematology
- Internal Medicine
Background:
- Polycythemia vera (PV) is a myeloproliferative neoplasm leading to erythrocytosis and hyperviscosity.
- Hypercoagulable states in PV significantly increase the risk of thrombotic events, including myocardial infarction.
- Managing acute coronary syndrome (ACS) in PV patients presents unique challenges due to persistent hypercoagulability.
Observation:
- A 59-year-old female presented with severe chest pain and ECG findings suggestive of ACS.
- Coronary angiography revealed occlusions in the LAD and RCA, with recurrent thrombus formation post-intervention.
- Elevated blood viscosity and subsequent investigations confirmed an underlying diagnosis of untreated polycythemia vera.
Findings:
- The patient's ACS was attributed to thrombotic complications of undiagnosed polycythemia vera.
- Aggressive management including perfusion balloon inflation, thrombus aspiration, dual antiplatelet therapy, and direct oral anticoagulants was employed.
- Successful treatment involved addressing both the acute thrombotic event and the underlying PV.
Implications:
- This case underscores the critical need for prompt diagnosis of polycythemia vera in patients presenting with seemingly idiopathic thrombotic events.
- Early recognition and comprehensive management strategies are essential for improving outcomes in PV patients with cardiovascular complications.
- Further research into optimized treatment protocols for managing thrombotic events in polycythemia vera is warranted.
Abstract:
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. <Learning objective: 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.>.
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