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Ann Thorac Surg 2001;71:1356-1358
© 2001 The Society of Thoracic Surgeons
a Department of Thoracic and Cardiovascular Surgery, Robert Debré Hospital, Reims, France
Accepted for publication May 1, 2000.
Address reprint requests to Dr Dabboussi, Service de Chirurgie Thoracique et Cardiovasculaire, Hôpital Robert Debré, Centre Hospitalier Universitaire de Reims, Avenue du Général Koenig, 51092 Reims Cedex, France
e-mail: mdabboussi{at}chu-reims.fr
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| Introduction |
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A 52-year-old hypertensive man was admitted to our hospital in November 1999 for intermittent left anterior atypical chest pain radiating into the back. He had a history of an anteroseptal myocardial infarction at the age of 35 years, and in 1982 at another institution, he had undergone a single reversed SVG to the left anterior descending coronary artery. In 1988, coronary angiography was performed because of a positive exercise test and revealed a complete occlusion of the left anterior descending coronary artery. The graft showed a diffuse ectasia, was patent, and provided flow to the first diagonal artery. That artery appeared to be less than 1 mm in diameter. Since that time, the patient had remained symptom free.
At this admission, a continuous murmur, particularly at the left sternal edge, was noted at the physical examination. The electrocardiogram showed sinus rhythm, anteroseptal Q waves, and left ventricular hypertrophy. The chest radiographs demonstrated a large suprahilar and left-sided anterior mediastinal mass. The thoracic computed tomographic scan revealed a 7.0 x 6.0-cm anterior mediastinal mass abutting the left side of the ascending aorta and adjacent to the main pulmonary artery. The vascular nature of the mass was revealed by partial enhancement (Fig 1). The coronary angiographic study showed obstructive changes with no major narrowing of the circumflex and right coronary arteries and their branches. The graft was not catheterized. Aortography indicated that the SVG was patent and demonstrated a fistulous communication between the graft and the main pulmonary artery (Fig 2).
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As a complication of these aneurysms, we note the development of a fistula to one chamber of the heart. Our review of the literature found four instances, one to the right ventricle [3], and three to the right atrium [46].
Early operation appears to be the treatment of choice to prevent complications [35]. Treatment includes resection of the aneurysm and further revascularization if necessary. Special care should be taken to prevent perioperative myocardial infarction by atheroembolism. No clinical signs of pulmonary embolization were noted in our patient. The myocardial enzymatic reaction was probably due to a limited infarction in the diagonal territory and could have been the result of atheroembolism or suppression of the graft.
In conclusion, the evolution of SVGs in coronary artery bypass operation, still has secrets to reveal. We think pulmonary artery fistula should be included as a late complication of SVG aneurysms.
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