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Ann Thorac Surg 1996;62:1830-1831
© 1996 The Society of Thoracic Surgeons
Division of Cardiothoracic Surgery, The University of Alberta, Edmonton, Alberta, Canada
Accepted for publication June 15, 1996.
A patient with Marfan's syndrome and previous Bentall repair for aortic dissection required orthotopic cardiac transplantation for end-stage cardiomyopathy. Postoperatively he suffered recurrent aortic dissection involving the transverse and descending aorta leading to tracheal and esophageal compression. He underwent successful surgical replacement of his ascending aorta, transverse arch, and descending aorta.
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