Late intervention in an asymptomatic pediatric patient with anomalous left coronary artery

John C Lam1, Michael Giuffre1, Kimberley A Myers1

  • 1John C Lam, Michael Giuffre, Kimberley A Myers, Department of Pediatrics, University of Calgary, Alberta Children's Hospital, Calgary, Alberta T3B 6A8, Canada.

World Journal of Cardiology
|September 18, 2014
PubMed

Insights

Anomalous left coronary artery from the pulmonary artery (ALCAPA) is rare in older children. Early surgical repair in late-diagnosed ALCAPA may improve heart function and prevent further damage.

Area of Science:

  • Pediatric Cardiology
  • Congenital Heart Disease
  • Cardiovascular Surgery

Background:

  • Anomalous left coronary artery from the pulmonary artery (ALCAPA) typically presents in infancy with severe left ventricle (LV) dysfunction.
  • Late diagnosis of ALCAPA is uncommon and presents unique clinical challenges.

Observation:

  • A 5-year-old patient with late-diagnosed ALCAPA presented with mild LV dilatation and minimal mitral regurgitation.
  • The patient had no significant LV dysfunction despite the anomalous coronary artery origin.

Findings:

  • Surgical intervention involving revascularization was performed.
  • Post-operative assessment showed no significant change in LV function or mitral regurgitation.

Implications:

  • The optimal timing for surgical intervention in late-diagnosed ALCAPA remains debated.
  • Early revascularization may potentially reverse ventricular and valvular dysfunction in these cases.
  • This case highlights the variability in presentation and potential for favorable outcomes with timely intervention.

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