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Ann Thorac Surg 1999;68:1392-1394
© 1999 The Society of Thoracic Surgeons
a Division of Thoracic and Cardiovascular Surgery, The Montreal General Hospital, McGill University, Montreal, Quebec, Canada
Address reprint requests to Dr Tchervenkov, The Montreal General Hospital, Rm L9-513, 1650 Cedar Ave, Montreal, PQ, Canada H3G 1A4
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| Introduction |
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A 19-year-old man was incidentally diagnosed with CoA at the age of 2 years by his physician on a routine physical examination. He underwent a standard subclavian flap angioplasty repair at the age of 7 years. There was no evidence of residual stenosis on regular physical and echocardiographic examinations. In 1994, a routine chest roentgenogram revealed an aortic aneurysm at the level of the aortic knob. Transesophageal echocardiography demonstrated a 7-cm aortic aneurysm at the level of the subclavian flap angioplasty. Subsequently, the patient underwent a magnetic resonance imaging that delineated the 7-cm by 8-cm proximal descending thoracic aortic aneurysm. The aortic arch and the distal descending thoracic aorta were of normal size. The aortic aneurysm was repaired by a left posterolateral thoracotomy through the fifth intercostal space. The fusiform aneurysm was identified extending from a point 1 cm distal to the origin of the left carotid artery for 7 cm of the proximal descending aorta. It was located at the site of the previous coarctation repair, involving the lateral wall of the aorta where the subclavian flap was used. Attenuated and fragmented fine Prolene suture material could be found embedded in the aortic wall. There was minimal adhesion between the aneurysm and the surrounding lung tissue. The aneurysm was resected and the aorta was reconstructed with a No. 20 Hemashield (Meadox Medical Inc, Oakland, NJ) interposition tube graft. The patient recovered uneventfully. Subsequent follow-up with magnetic resonance imaging revealed a normal reconstructed thoracic aorta.
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Aneurysm formation represents another rare but life-threatening late complication after CoA repair. It is particularly prevalent in patients who had a synthetic patch aortoplasty. In a recent review of the results of CoA repair involving 891 patients, aortic aneurysm developing at the site of repair was noted in 48 patients (5.4%), 90% (43 patients) of which had had synthetic patch aortoplasty [2]. The remaining 5 patients were confined to patients having coarctectomy and end-to-end anastomosis or prosthetic graft interposition. The incidence of aneurysmal formation after synthetic (Dacron) patch aortoplasty increased with the duration of follow-up: 6 patients were detected within 5 years after CoA repair, 32 patients (66.7%) were documented during 6- to 16-year observation periods. In another series, five aneurysms were detected in 38 patients (between 6 and 18 years postoperatively) in whom a Dacron patch had been used for primary CoA repair or to revise an earlier repair [4]. These aneurysms typically occurred in the aortic wall opposite the synthetic patch. These reports identified the serious complications of aneurysm formation associated with synthetic patch angioplasty and suggested to abandon this technique and called for a careful lifelong follow-up of patients who had this type of CoA repair.
Martin and colleagues [5] reported in 1988 aortic aneurysm in 3 patients at the site of previous CoA repair by SFA 2 to 3 years after operation. Two other case reports [6, 7] published within the past 4 years also documented true aneurysm formation at the site of CoA repair 5 to 12 years after SFA. The exact location of the aneurysm in relation to the flap and the native aortic wall were not mentioned in these reports. We noted a true aneurysmal dilatation involving the lateral aortic wall precisely at the site of the subclavian artery flap and not in the native aortic wall where the coarct shelf would have been.
Including our own patient, to date, there have only been 6 patients with aortic aneurysmal formation associated with SFA reported in the literature. Considering the popularity of this procedure in the past and the paucity of reported cases of aneurysm at the site of previous CoA SFA repair, this remains an uncommon complication of this procedure. It is, however, prudent to recommend that patients with SFA repair for CoA should be followed for life so that late aneurysm can be detected and managed accordingly.
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