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Congenital intrathoracic left ventricular diverticulum in an adult
C Suilen1, B Friedli, W Rutishauser
1University Hospital, Geneva, Switzerland.
Chest
|September 1, 1990
Insights
A rare congenital heart defect, left ventricular diverticulum, was found in an adult woman with no risk factors. Surgical resection confirmed normal cardiac layers, highlighting its extreme rarity in adults.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Cardiac Surgery
Background:
- Congenital heart anomalies are typically diagnosed in childhood.
- Intrathoracic left ventricular diverticulum is an exceptionally rare congenital cardiac malformation.
Observation:
- A 53-year-old woman presented with an incidentally discovered intrathoracic left ventricular diverticulum.
- The diverticulum had a narrow, elongated connection to the left ventricular cavity.
- The patient had no traditional risk factors for coronary artery disease.
Findings:
- Coronary angiography demonstrated normal coronary arteries, ruling out ischemic causes.
- Surgical resection of the diverticulum revealed intact, normal cardiac layers (endocardium, myocardium, epicardium).
- Histopathological examination confirmed the absence of pathological changes within the diverticulum wall.
Implications:
- This case underscores that congenital heart anomalies can remain undiagnosed into adulthood.
- The successful resection and identification of normal cardiac layers in this rare adult presentation offer valuable insights for surgical planning.
- Further research into the embryology and long-term implications of such rare adult congenital cardiac findings is warranted.
Abstract:
A 53-year-old woman without any risk factors for coronary artery disease was found to have a congenital intrathoracic left ventricular diverticulum with a narrow long connection to the left ventricular cavity. Coronary angiography revealed normal coronary arteries. The diverticulum was resected and showed three normal cardiac layers. This is an extremely rare finding in the adult population.