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Patients with Marfan syndrome were a well-known risk population to develop aortic root aneurysm and aortic dissection through entire life span. Repeated operations for ascending, descending and abdominal aortic pathology were not uncommon. We present a case report of a total thoracoabdominal aortic replacement in a Marfan patient following heart transplantation and hemiarch repair. We achieved a successful...
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