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1.
Journal of Cardiovascular Ultrasound ; : 49-51, 2012.
Article in English | WPRIM | ID: wpr-144951

ABSTRACT

We present a case of persistent left superior vena cava, anomalous right pulmonary venous connection to the right-sided superior vena cava and sinus venosus atrial septal defect detected by computed tomography (CT) pulmonary angiography and echocardiography. These defects were surgically corrected using a double-patch technique. In fact, CT can provide anatomical information about a complex anomaly in the systemic and pulmonary vasculatures. Though modern imaging techniques are useful for detecting complex cardiovascular disease, careful echocardiographic examination should be performed to diagnose complex cardiac anomalies.


Subject(s)
Angiography , Cardiovascular Diseases , Echocardiography , Heart Septal Defects, Atrial , Vascular Diseases , Vena Cava, Superior
2.
Journal of Cardiovascular Ultrasound ; : 49-51, 2012.
Article in English | WPRIM | ID: wpr-144938

ABSTRACT

We present a case of persistent left superior vena cava, anomalous right pulmonary venous connection to the right-sided superior vena cava and sinus venosus atrial septal defect detected by computed tomography (CT) pulmonary angiography and echocardiography. These defects were surgically corrected using a double-patch technique. In fact, CT can provide anatomical information about a complex anomaly in the systemic and pulmonary vasculatures. Though modern imaging techniques are useful for detecting complex cardiovascular disease, careful echocardiographic examination should be performed to diagnose complex cardiac anomalies.


Subject(s)
Angiography , Cardiovascular Diseases , Echocardiography , Heart Septal Defects, Atrial , Vascular Diseases , Vena Cava, Superior
3.
Journal of the Korean Radiological Society ; : 725-727, 2000.
Article in Korean | WPRIM | ID: wpr-74397

ABSTRACT

Anomalous unilateral single pulmonary vein is a rare abnormality of the pulmonary venous system characterized by a tortuous pulmonary venous confluence which never crosses the diaphragm and drains all arterialized blood from a lung to the left atrium, into which it normally flows. Cardiac and pulmonary anomalies are not associated. We report a case in which this condition was comfirmed by the findings of chest radiography, computed tomography, and magnetic resonance angiography.


Subject(s)
Diaphragm , Heart Atria , Lung , Magnetic Resonance Angiography , Pulmonary Veins , Radiography , Thorax
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