First case of intracardiac foregut cyst occurring in the left-ventricular outflow tract
Jennifer H Huang1, Erin R Rudzinski, Mary S Minette
1Department of Pediatric Cardiology, Doernbecher Children's Hospital, 3604 SE Morrison Street, Portland, OR, 97239, USA, jenniferhhuang@gmail.com.
Insights
A rare intracardiac foregut cyst caused critical aortic stenosis and left-ventricular outflow obstruction (LVOT) in an infant. This case highlights the potential for foregut cysts to cause severe cardiac issues, necessitating surgical intervention.
Area of Science:
- Pediatric Cardiology
- Congenital Heart Disease
- Surgical Pathology
Background:
- Critical aortic stenosis in neonates often requires surgical intervention.
- Left-ventricular outflow obstruction (LVOT) is a significant concern in pediatric cardiac patients.
- Intracardiac masses are uncommon causes of congenital heart defects.
Observation:
- An 11-day-old infant presented with subaortic mass and critical aortic stenosis.
- Recurrent severe LVOT and heart failure occurred at 3 months of age.
- Redo surgery revealed an intracardiac foregut cyst as the obstructing mass.
Findings:
- The resected mass was identified as an intracardiac foregut cyst.
- This cyst was the cause of both initial critical aortic stenosis and subsequent recurrent LVOT.
- This represents the first reported case of an intracardiac foregut cyst causing LVOT.
Implications:
- Foregut cysts should be considered in the differential diagnosis of neonatal cardiac masses and outflow obstruction.
- Early diagnosis and surgical management are crucial for improving outcomes in affected infants.
- This case expands the understanding of rare causes of congenital heart disease and LVOT.
Abstract:
An 11 day-old female infant underwent resection of a mass in the subaortic region secondary to critical aortic stenosis. At 3 months of age, recurrent severe left-ventricular outflow obstruction (LVOT) in the setting of heart failure prompted redo surgery, and the resected mass revealed an intracardiac foregut cyst, which is a rare finding. To our knowledge, this is the first case describing obstruction of the LVOT.
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