Hoarseness as the initial clinical presentation of anomalous left coronary artery from the pulmonary artery
D R Allen1, R M Schieken, M T Donofrio
1Division of Pediatric Cardiology, Department of Pediatrics, Virginia Commonwealth University Health System, PO Box 980026, Richmond, VA 23298, USA.
Insights
An unusual congenital heart defect, anomalous left coronary artery from the pulmonary artery, can present with a hoarse cry in infants. Early diagnosis is critical to prevent severe heart damage and mortality.
Area of Science:
- Cardiology
- Pediatric Cardiology
- Congenital Heart Disease
Background:
- Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital heart defect.
- Untreated ALCAPA often leads to severe myocardial ischemia, significant morbidity, and mortality in infants.
Observation:
- A 2-month-old infant presented with an unusual symptom: a hoarse cry.
- This presentation was linked to a diagnosed case of ALCAPA.
Findings:
- The hoarse cry was theorized to result from recurrent laryngeal nerve impingement.
- Pulmonary artery dilatation secondary to ALCAPA was the likely cause of nerve impingement.
Implications:
- This case highlights that congenital heart disease can manifest with atypical symptoms.
- It underscores the importance of considering serious cardiac anomalies even with unusual presenting complaints.
Abstract:
Anomalous origin of the left coronary artery from the pulmonary artery is a rare congenital anomaly that, if left untreated, will most often result in severe myocardial ischemia and significant morbidity and mortality. We report an unusual presentation of this defect in a 2-month-old infant who had an initial complaint of a "hoarse cry." We theorize that impingement of the recurrent laryngeal nerve due to dilatation of the pulmonary artery was the most likely etiology of the patient's symptoms. This case serves as an important reminder that serious congenital heart disease may present with any number of complaints and unusual findings.
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