Subtotal Cor Triatriatum on Dual-Source Computed Tomography
نویسندگان
چکیده
منابع مشابه
Asymptomatic cor triatriatum incidentally revealed by computed tomography.
We report a case of asymptomatic cor triatriatum in a 75-year-old man in whom the anomaly was incidentally revealed by computed tomography (CT). To our knowledge, this patient is the oldest case reported and the only such case in which the anomaly was demonstrated by CT.
متن کاملEvaluating adult cor triatriatum with total anomalous pulmonary venous connections by multidetector computed tomography angiography.
A 19-year-old female patient was admitted to our hospital with dyspnea, chest pain, and shortness of breath. A chest radiograph showed mild cardiomegaly. Echocardiography revealed an extra chamber in the heart. To evaluate this abnormality, ECG-gated 16-detector-row computed tomography angiography was performed. Multidetector computed tomography (MDCT), showing cor triatriatum with total anomal...
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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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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: The Annals of Thoracic Surgery
سال: 2019
ISSN: 0003-4975
DOI: 10.1016/j.athoracsur.2018.09.029