Editorial: Cor triatriatum: An intraoperative diagnosis
نویسندگان
چکیده
منابع مشابه
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 ...
متن کامل[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...
متن کاملCor 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...
متن کاملCor 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...
متن کاملCor 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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ژورنال
عنوان ژورنال: Journal of Cardiology Cases
سال: 2014
ISSN: 1878-5409
DOI: 10.1016/j.jccase.2013.11.001