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The base is formed by the coronary sinus orifice and the vestibule of the right atrium, and the hypotenuse is formed by the tendon of Todaro, which is often a continuation off the Eustachian valve. Other structures near to it are the membranous septum and the Eustachian ridge. Variations in the size of Koch's triangle are common.
This can happen within the heart (intracardiac) where it drains into the coronary sinus or right atrium, or below it (infracardiac) where it drains into the liver at the portal or hepatic vein. The anomalous connection causes low blood oxygenation and limitation of venous return to the heart. [3]
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
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 superior vena cava (SVC) is the superior of the two venae cavae, the great venous trunks that return deoxygenated blood from the systemic circulation to the right atrium of the heart. It is a large-diameter (24 mm) short length vein that receives venous return from the upper half of the body, above the diaphragm.
The early bulbus cordis is formed by the fifth week of development. [4] The truncus arteriosus is derived from it later. [2]The adjacent walls of the bulbus cordis and ventricle approximate, fuse, and finally disappear, and the bulbus cordis now communicates freely with the right ventricle, while the junction of the bulbus with the truncus arteriosus is brought directly ventral to and applied ...
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]