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.

ESC Heart Failure
|July 9, 2022
PubMed

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.

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