Successful repair of symptomatic cor triatriatum dexter in infancy

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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 ...

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A complicated case of cor triatriatum dexter.

over the right chest wall, not obviously associated with any clinical abnormality. Ten days after admission, oedema of the face became apparent. Emination revealed a swollen right arm, a much enlarged and tender right breast, associated with dilated veins in the chest wall, and non-pulsatile distension of the neck veins. A diagnosis of superior vena caval obstruction was made. The liver was enl...

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[Cor triatriatum dexter of an adult].

Cor triatriatum dexter is a rare congenital malformation in which a membrane divides the right atrium into two chambers. The membrane represents a persistence of the right sinus venosus valve (RSV). Normally the RSV regresses between the 9th and 15th week of gestation, as the cephalic portion forms the crista terminalis and the caudal portion develops into the Eustachian and Thebesian valve. An...

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Cor triatriatum dexter with imperforate Ebstein's anomaly.

A case of cor triatriatum dexter is described in which the anomalous right atrial partition is identified as the right venous valve; there is an associated anomaly of the right atrioventricular valve which combines features of Ebstein's anomaly, and an atypical, imperforate, tricuspid atresia.

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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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ژورنال

عنوان ژورنال: The Journal of Thoracic and Cardiovascular Surgery

سال: 1983

ISSN: 0022-5223

DOI: 10.1016/s0022-5223(19)38912-3