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J Thorac Cardiovasc Surg 2009;137:e34-e36
© 2009 The American Association for Thoracic Surgery
Brief Communication |
Department of Thoracic and Cardiovascular Surgery, Guro Hospital, Korea University Medical Center, Seoul, Republic of Korea
Received for publication July 18, 2008; accepted for publication July 26, 2008. * Address for reprints: Man-Jong Baek, MD, Department of Thoracic and Cardiovascular Surgery, Guro Hospital, Korea University Medical Center, Guro 2-Dong, Guro-Gu, Seoul, Republic of Korea, 152-703. (Email: mdmjbaek@korea.ac.kr).
| The first 20% of the full text of this article appears below. |
Concomitant thoracic reconstruction in patients with Marfan syndrome, pectus excavatum, and associated aortic or cardiac surgery poses a major clinical challenge.
Clinical Summary
A 39-year-old man was seen with dyspnea in March 2008. He had no history of musculoskeletal disease or heart disease apart from Marfanoid features according to the Ghent criteria1
seen on general examination: kyphoscoliosis, pectus excavatum, arachnodactyly, severe myopia, and diastolic murmur on the apex. Routine laboratory values were also unremarkable. Transthoracic and transesophageal echocardiography showed severely dilated ascending aorta, severe aortic regurgitation, moderate mitral and tricuspid regurgitation, and a small type II atrial septal defect. Computed tomographic scans showed a fusiform aneurysm of the proximal ascending aorta with a maximum diameter of 73 mm, severe pectus excavatum (pectus index of 32.6; Figure 1
), thoracolumbar scoliosis, and dural ectasia of the lumbosacral area.
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