A Rare Case of a Type IV Dual Left Anterior Descending Artery and Ectopic Left Anterior Descending and Circumflex

Muhammad Mansoor1, Waqar Ahmad Khan1, Fakhar Abbas2

  • 1National Institute of Cardiovascular Disorders, Karachi, Pakistan.

Insights

Congenital anomalous coronary arteries (CACAs) are usually benign but can cause severe cardiac events. This case highlights a rare CACA presentation in a 62-year-old man, successfully treated with bypass surgery.

Area of Science:

  • Cardiology
  • Cardiovascular Surgery
  • Medical Genetics

Background:

  • Congenital anomalous coronary arteries (CACAs) represent anatomical variations in coronary vasculature.
  • While often benign, certain CACAs can lead to severe ischemic events, including myocardial infarction and sudden cardiac death.

Observation:

  • A 62-year-old male presented with acute substernal chest pain, ECG changes (Q waves in leads II, III, aVF), and elevated troponin I.
  • Left heart catheterization revealed triple vessel disease with significant left main coronary artery (LMCA) stenosis.
  • Anatomical findings included anomalous origin of the left anterior descending (LAD) and left circumflex arteries from the right coronary ostium, and a rudimentary type IV dual LAD from the LMCA.

Findings:

  • The patient had complex congenital coronary anomalies combined with significant atherosclerotic disease.
  • Surgical intervention involved coronary artery bypass graft (CABG) surgery.

Implications:

  • This case underscores the importance of recognizing and managing complex CACAs, especially when associated with atherosclerotic disease.
  • Successful surgical revascularization can effectively treat symptomatic patients with these rare anomalies.
  • Further research into the long-term outcomes of managing combined CACAs and coronary artery disease is warranted.

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