Project description:A 55-year-old woman admitted with symptoms of right heart failure received a diagnosis of double-chambered right ventricle and a ventricular septal defect with aortic and pulmonic valve endocarditis. This case highlights the use of multimodality imaging and importance of adult congenital heart disease expertise in the diagnosis and treatment of such patients. (Level of Difficulty: Intermediate.).

| S-EPMC10429273 | biostudies-literature

Isolated Double-Chambered Right Ventricle - A Rare Entity.

Project description:A double-chambered right ventricle (DCRV) is a rare congenital heart disease and an uncommon cause of congestive heart failure. An anomalous muscle band divides the right ventricle into two cavities: the proximal high-pressure chamber and the distal low-pressure chamber. Most cases are diagnosed and treated during childhood. Furthermore, there is a tendency for progression, if not treated early. Echocardiography is considered useful for the diagnosis of this ailment. Most of the patients have associated congenital anomalies, such as ventricular septal defect, pulmonary stenosis, and subaortic stenosis. Isolated DCRV is a rare entity. Hence, we report a case of an isolated DCRV in an adult patient.

| S-EPMC7799069 | biostudies-literature

Acquired double-chambered right ventricle.

Project description: Not available

| S-EPMC8084404 | biostudies-literature

From Double-Chambered Right Ventricle to Double-Chambered Left Ventricle: Unusual Evolution of a Ventricular Septal Defect.

Project description:We present the first imaging registry of the progressive isolation of an apical chamber of the right ventricle caused by the hypertrophy of the moderator band generated from the hemodynamic effect of a ventricular septal defect, leaving the apex of the right ventricle as an accessory chamber of the left ventricle. (Level of Difficulty: Advanced.).

| S-EPMC9588453 | biostudies-literature

A rare case of double-chambered right ventricle associated with ventricular septal defect and congenital absence of the pulmonary valve.

Project description:Double-chambered right ventricle (DCRV) is a rare congenital heart disorder involving 2 different right ventricle (RV) pressure compartments that is often associated with ventricular septal defect (VSD). Usually, the obstruction is caused by an anomalous muscle bundle crossing the RV from the interventricular septum to the RV free wall. We are reporting a case of double-chambered right ventricle associated with ventricular septal defect and congenital absence of the pulmonary valve, a rare form of congenital infundibular pulmonary stenosis. In addition to ventricular septal defect, our patient had congenital absence of the pulmonary valve, which is very unusual and has never been reported to our knowledge.

| S-EPMC3966724 | biostudies-literature

Revisiting Folger's pouch in double-chambered right ventricle.

Project description:Folger's pouch is a right ventricular outflow pouch arising from the distal low-pressure chamber in double-chambered right ventricle. It is rarely described on echocardiogram due to difficult visualization and lack of knowledge of its existence. Retrospective assessment of echocardiogram after an angiocardiographic evaluation demonstrates the pouch in a modified high parasternal view.

| S-EPMC10158473 | biostudies-literature

Double-Chambered Right Ventricle in Adulthood: A Case Series.

Project description: Not available

| S-EPMC10954581 | biostudies-literature

Quadricuspid Aortic Valve: A Rare Cause of Aortic Regurgitation.

Project description: Not available

| S-EPMC7451882 | biostudies-literature

'Matrioska left ventricle': a case of double-chambered left ventricle with double mitral valve apparatus.

Project description: Not available

| S-EPMC9303002 | biostudies-literature