Myocardial infarction with non-obstructive disease and anomalous coronary origin: look for the common in the uncommon
Gindomenico Disabato1,2, Antonia Camporeale2, Mauro Lo Rito3
1University of Pavia, Pavia, Italy.
Insights
Congenital coronary artery anomalies (CAA) lack standardized management, especially when detected during myocardial infarction with non-obstructive coronary arteries (MINOCA). This case highlights the need for precise risk stratification in complex CAA presentations.
Area of Science:
- Cardiology
- Cardiovascular Surgery
- Medical Imaging
Background:
- Management of congenital coronary artery anomalies (CAA) is challenging due to their rarity and diverse presentations.
- Coronary artery anomalies (CAA) are not integrated into current algorithms for myocardial infarction with non-obstructive coronary arteries (MINOCA).
- Surgical repair is suggested for symptomatic anomalous aortic origin of a coronary artery, complicating MINOCA management.
Observation:
- A 35-year-old male presented with suspected myocardial infarction.
- Coronary angiography revealed an anomalous origin of the left coronary artery from the right Valsalva sinus with a pre-pulmonic course.
- Stress cardiac magnetic resonance imaging showed recent myocarditis but no inducible ischaemia.
Findings:
- The case demonstrates a complex presentation of congenital coronary artery anomaly (CAA) in the context of myocardial infarction with non-obstructive coronary arteries (MINOCA).
- Accurate diagnosis and risk stratification are crucial, particularly when clinical scenarios are confounded by conditions like myocarditis.
- The interplay between CAA, MINOCA, and myocarditis necessitates careful evaluation beyond standard algorithms.
Implications:
- This case underscores the need for updated clinical guidelines to incorporate CAA management within MINOCA protocols.
- Accurate risk stratification is essential for determining appropriate treatment strategies in patients with complex CAA.
- Further research is required to standardize the approach to congenital coronary artery anomalies presenting with acute coronary syndromes.
Abstract:
Management of congenital coronary artery anomalies (CAA) is not standardized due to the variety of conditions included and their rare prevalence. Detection of CAA during myocardial infarction with non-obstructive coronary arteries (MINOCA) may induce clinicians to address the patient for surgery as CAA is not included in any algorithm1,2 for the management of MINOCA and American Association for Thoracic Surgery evidence-based guidelines suggest surgical repair for patients with anomalous aortic origin of a coronary artery and symptoms compatible with myocardial ischaemia.3 We present the case of a 35-year-old man with an anomalous origin of left coronary artery from right Valsalva sinus with pre-pulmonic course detected during urgent coronary angiography for suspected myocardial infarction. Stress cardiac magnetic resonance did not show signs of ischaemia at high-dose dobutamine but did reveal a recent myocarditis. This clinical case highlights the need for accurate risk stratification in CAA especially when confounding clinical scenarios co-exist.
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