Cor Triatriatum sinester

Cor triatriatum sinister.

C triatriatum is a very rare congenital cardiac anomaly with no known associated genetic abnormalities. Cor triatriatum is generally an isolated anomaly but may be associated with anomalous pulmonary venous return in approximately 10% of patients, patent ductus arteriosus, left superior vena cava, ventricular septal defects, Shone syndrome, tricuspid atresia, Ebstein malformation, atrioventricu...

Cor Triatriatum Sinistrum

Figure 1 – A) Transthoracic echocardiogram showing cor triatriatum: proximal and distal left atrium separated by a membrane (Pointing white arrow), LA: left atrium; LV: left ventricle; RV: right ventricle; RA: right atrium. B) Transesophageal echocardiogram showing cor triatriatum: proximal and distal left atrium separated by a membrane (Pointing white arrow), LA: left atrium; LV: left ventricl...

Cor triatriatum dexter in adults?

Rev Esp Cardiol. 2010;63(12):1510-6 1515 On the other hand, in the fetus and in childhood it is exceptional to find an obstructive CTD without associate anomalies, and in our experience it is also exceptional to find it associated with right-sided heart malformations. That perception is corroborated by the lack of description of this issue, limited to a few cases published in literature.4-6 In ...

Cor triatriatum with pericardial agenesis.

Coexistence of Cor triatriatum sinistrum and a prominent Eustachian valve mimicking a Cor triatriatum dextrum

Cor triatriatum is among the rarest of all congenital cardiac abnormalities accounting for 0.1-0.4% of all congenital heart disease. Its coexistence with a very prominent Eustachian valve which mimics a Cor triatriatum dextrum is an exceptionally rare finding in an asymptomatic adult. We report the case of a 44 year old male who presented to our department on observing a pulse rate of 44 beats ...