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Ann Thorac Surg 1996;62:1526-1528
© 1996 The Society of Thoracic Surgeons
St. Vincent Hospital, Portland, Oregon
Accepted for publication June 8, 1996.
Primary tumors of the aorta are rare and are usually malignant. Thirty-three cases are reported in the world literature, of which 2 are myxomas. The diagnosis is difficult and is commonly made postoperatively or at autopsy. We present a case of intraluminal aortic myxoma that presented as recurrent arterial emboli and was managed successfully. This case showed the sensitivity of magnetic resonance imaging and transesophageal echocardiography in diagnosis.
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