Double-chambered right ventricle is a congential malformation caused by an anomalous muscle band obstructing the right ventricular outflow tract. Most reported cases of this condition have been diagnosed in infants, or adolescents. We encountered a 61-year-old woman with a double-chambered right ventricle, associated with a large interventricular septal aneurysm, which is a rare complication. The right ventricular obstruction was corrected with surgery.
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http://dx.doi.org/10.1007/BF02481440 | DOI Listing |
Cureus
January 2025
Cardiovascular Surgery, Nihon University School of Medicine, Tokyo, JPN.
[This retracts the article DOI: 10.7759/cureus.74051.
View Article and Find Full Text PDFKardiol Pol
January 2024
Department of Cardiology and Electrotherapy, Faculty of Medicine, Medical University of Gdansk, Gdańsk, Poland.
Cureus
November 2024
Cardiovascular Surgery, Nihon University School of Medicine, Tokyo, JPN.
Double-chambered right ventricle (DCRV) is a congenital heart disease. Most cases of DCRV are complicated by another congenital cardiac anomaly. Mostly, a ventricular septal defect (VSD) is the usual comorbidity.
View Article and Find Full Text PDFAsian J Surg
November 2024
Department of Cardiovascular Surgery, Binzhou Medical University Hospital, Binzhou, Shandong province, 256600, China.
CASE (Phila)
September 2024
The CardioVascular Center, Tufts Medical Center, Boston, Massachusetts.
• DCRV is a rare finding in older adults. • DCRV can be seen in association with a wide range of cardiac abnormalities. • Cardiac imaging characterizes anatomy, hemodynamics, and associated cardiac lesions.
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