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Coronary artery disease associated with factor V Leiden mutation: a case report
Roberto Muniz Ferreira1, Paolo Blanco Villela1, Jose Ary Boechat2
1Department of Cardiology, Samaritano Hospital, Rio de Janeiro, RJ, Brasil.
A young woman with coronary artery disease was found to have the factor V Leiden mutation. This case highlights the need for further research into managing young patients with atherosclerosis and hereditary thrombophilia.
Area of Science:
- Cardiovascular Medicine
- Genetics
- Thrombophilia
Background:
- Coronary artery disease (CAD) is increasing in young adults.
- Traditional risk factors are often present, but new associations are emerging.
- The link between factor V Leiden mutation and atherosclerosis is debated.
Observation:
- A 37-year-old woman with no prior symptoms developed rapid angina.
- Coronary angiography showed significant left anterior descending artery obstruction.
- Optical coherence tomography revealed a vulnerable atherosclerotic plaque.
Findings:
- The patient underwent successful coronary angioplasty with a drug-eluting stent.
- Thrombophilia screening revealed a heterozygous factor V R506Q mutation (factor V Leiden).
- No prior thromboembolic events were noted.
Implications:
- This case underscores the potential role of factor V Leiden in early-onset atherosclerosis.
- Management strategies for young patients with atherosclerosis and hereditary thrombophilia require further investigation.
- Understanding these associations is crucial for personalized cardiovascular risk assessment.
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