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Total anomalous pulmonary venous connection, also known as total anomalous pulmonary venous return, is a rare cyanotic congenital heart defect in which the pulmonary veins drain into the right side of the heart instead of the left, as is usually seen. This can happen within the heart (intracardiac) where it drains into the coronary sinus or ...
It is an anatomical area located at the base of the right atrium, and its boundaries are the coronary sinus orifice, tendon of Todaro, and the septal leaflet of the right atrioventricular valve (also known as the tricuspid valve). [2] It is anatomically significant because the atrioventricular node is located at the apex of the triangle. The ...
Changes in the conduction pathways of the heart can result in right axis deviation. For example, an accessory pathway from the left atrium to the left ventricle, as in Wolff-Parkinson-White Syndrome, will result in the left ventricle finishing depolarisation earlier than the right. [16]
The right atrial appendage (lat: auricula atrii dextra) is located at the front upper surface of the right atrium. Looking from the front, the right atrial appendage appears wedge-shaped or triangular. Its base surrounds the superior vena cava. [6] The right atrial appendage is a pouch-like extension of the right atrium and is covered by a ...
English: Diagram of the human heart. 1. Superior vena cava 2. 4. Mitral valve 5. Aortic valve 6. Left ventricle 7. Right ventricle 8. Left atrium 9. Right atrium 10. Aorta 11. Pulmonary valve 12. Tricuspid valve. 13. Inferior vena cava
Scimitar syndrome, or congenital pulmonary venolobar syndrome, is a rare congenital heart defect characterized by anomalous venous return from the right lung (to the systemic venous drainage, rather than directly to the left atrium). [1] This anomalous pulmonary venous return can be either partial (PAPVR) or total (TAPVR).
Occasionally, the eustachian valve crosses the floor of the right atrium from the orifice of the IVC and inserts into the lower portion of the interatrial septum adjacent to the atrioventricular valves. [2] However, higher insertion of a giant eustachian valve, which mimics the echocardiographic appearance of divided right atrium, is very rare.
Uhl anomaly is a rare cardiac malformation that was first identified by Dr. Henry Uhl in 1952. It is characterized by the absence of the right ventricle (RV) myocardium, either entirely or partially, and the replacement of the RV myocardium by nonfunctional fibroelastic tissue that resembles parchment. [1]