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Isolated double-chambered right ventricle in a young adult
Jung-Gil Park1, Han-Jun Ryu, Yeun-Su Jung
1Department of Internal Medicine, Daegu Fatima Hospital, Daegu, Korea.
Insights
Double-chambered right ventricle (DCRV), a rare congenital heart defect, can be asymptomatic in adults. This case highlights diagnosis using echocardiography, cardiac catheterization, and MRI.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Adult Congenital Heart Disease
Background:
- Double-chambered right ventricle (DCRV) is a rare congenital anomaly.
- It involves anomalous muscle bundle division of the right ventricle into high-pressure inlet and low-pressure outlet portions.
Purpose of the Study:
- To report a case of isolated DCRV.
- To describe the diagnosis of asymptomatic adult DCRV.
Main Methods:
- Echocardiography
- Cardiac catheterization
- Cardiac magnetic resonance imaging (CMR)
Main Results:
- Isolated DCRV was diagnosed in an adult.
- The patient was asymptomatic.
Conclusions:
- DCRV can remain undiagnosed into adulthood.
- Advanced imaging and hemodynamic assessment are crucial for diagnosing DCRV.
Abstract:
Double-chambered right ventricle (DCRV) is a rare congenital heart disorder in which the right ventricle is divided by an anomalous muscle bundle into a high pressure inlet portion and a low pressure outlet portion. We report a case of isolated DCRV without symptoms in adulthood, diagnosed through echocardiography, cardiac catheterization and cardiac magnetic resonance imaging.
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