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Ann Thorac Surg 2004;77:1101
© 2004 The Society of Thoracic Surgeons
a Department of Thoracic and Cardiovascular Surgery, Hokkaido Prefectural Kushiro Hospital, Kushiro, Japan
b Department of Thoracic and Cardiovascular Surgery, Sapporo Medical University School of Medicine, Sapporo, Japan
* Address reprint requests to Dr Hachiro, Department of Thoracic and Cardiovascular Surgery, Sapporo Medical University School of Medicine, South 1, West 16, Chuo-ku, Sapporo 060-8543, Japan
e-mail: hachiro@rf6.so-net.ne.jp
| The first 20% of the full text of this article appears below. |
A 30-year-old man with Marfan syndrome was admitted with severe chest pain 3 years after replacement of the entire aorta. The patient's medical history included bilateral bullectomy when he was 16 years old; a composite graft repair of the aortic root and total arch replacement with a distal elephant
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