Cor Triatriatum: A Tale of Two Membranes

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Cor triatriatum dexter: two-dimensional echocardiographic diagnosis.

Cor triatriatum dexter is a malformation resulting from lack of normal regression of the embryonic right valve of the sinus venosus. In this situation, the right atrium is divided by a membrane into two chambers. Two-dimensional echocardiography was used in the antemortem diagnosis of this rare cardiac anomaly in a neonate. Associated cardiac lesions were also documented. The patient died, and ...

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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...

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A complicated case of cor triatriatum dexter.

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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 ...

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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...

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ژورنال

عنوان ژورنال: CASE

سال: 2019

ISSN: 2468-6441

DOI: 10.1016/j.case.2018.08.003