Related Experiment Video

Updated: Feb 15, 2026

Direct Re-implantation of Left Coronary Artery into the Aorta in Adults with Anomalous Origin of Left Coronary Artery from the Pulmonary Artery ALCAPA
13:10

Direct Re-implantation of Left Coronary Artery into the Aorta in Adults with Anomalous Origin of Left Coronary Artery from the Pulmonary Artery ALCAPA

Published on: April 24, 2017

19.3K

Adult presentation of ALCAPA: Echo and CT diagnosis

Edmund Kenneth Kerut1, Philip G Kogos2, Jason H Anderson3

  • 1Heart Clinic of Louisiana, Marrero, LA, USA.

Echocardiography (Mount Kisco, N.Y.)
|January 23, 2018
PubMed

Insights

A rare congenital heart defect, anomalous left coronary artery from the pulmonary artery (ALCAPA), was diagnosed in a young male presenting with aborted sudden death. Advanced imaging confirmed ALCAPA

Area of Science:

  • Cardiology
  • Congenital Heart Disease
  • Medical Imaging

Background:

  • Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital heart anomaly.
  • It can lead to significant morbidity and mortality if not diagnosed and treated early.

Observation:

  • A 20-year-old male presented with aborted sudden death, a critical manifestation of ALCAPA.
  • Diagnostic imaging was crucial for identifying this rare coronary anomaly.

Findings:

  • Thoracic echocardiography and cardiac computed tomographic angiography revealed characteristic ALCAPA findings.
  • These included a dilated, tortuous right coronary artery, septal and epicardial collateral vessels, and anomalous origin of the left coronary artery from the pulmonary artery.

Implications:

  • Accurate diagnosis of ALCAPA using complementary imaging modalities is essential for timely surgical intervention.
  • Early detection and surgical correction can prevent life-threatening cardiac events.

Keywords:
ALCAPAsudden death

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