- Case report
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Internal mammary artery dilatation in a patient with aortic coarctation, aortic stenosis, and coronary disease. Case report
© Alvarez et al; licensee BioMed Central Ltd. 2011
- Received: 13 December 2010
- Accepted: 17 April 2011
- Published: 17 April 2011
The ideal surgical approach is unclear in adult patients with coarctation of the aorta that is associated with other cardiovascular pathologies that require intervention. Standard median sternotomy allows simultaneous, coronary revascularization surgery, valve replacement and repair of aortic coarctation. However the collateral circulation and the anatomy of the mammary arteries must be determined, to avoid possible complications. We report a case of a 69 year-old man with aortic coarctation, aortic stenosis, coronary artery disease and internal mammary artery dilatation who underwent concomitant surgical procedures through a median sternotomy.
- Aortic Valve
- Aortic Stenosis
- Subclavian Artery
- Collateral Circulation
- Bicuspid Aortic Valve
The ideal surgical approach is unclear for adults patients with aortic coarctation whom have other associated cardiovascular pathologies. These patients have extensive collateral circulation, mainly from branches of the subclavian artery . Long-term complications include aneurysmal dilatation of collateral circulation, which may eventually rupture. This can be a problem when a median sternotomy is performed.
Although coarctation of the aorta is a congenital heart defect, it is frequently diagnosed in adulthood because patients can remain symptom-free for many years. However, hypertension is common and more severe in older than in younger patients, and as in this case study, older patients with coarctation of the aorta may present with heart failure. Collateral circulation between the part of the aorta proximal to the coarctation and that distal to it, it is one of the striking features of coarctation. There is usually extensive collateral circulation in adults with coarctation, and the source is mainly due to branches of both subclavian arteries, particularly the internal thoracic and vertebral arteries. In these patients, long-term complications include aortic aneurysm formation and aneurysmal dilatation of the collateral circulation, which may eventually rupture . Overall the prevalence of aneurysm is about 10% by the end of the second decade of life, 20% by the end of the third decade, and probably even higher in older patients . When an adult patient with aortic coarctation needs median sternotomy for cardiac surgery, Laks et al  suggested that magnetic resonance angiography with three dimensional computerized reconstruction to assess the transverse arch, isthmus, and descending aorta is often useful. We think it is necessary to define the anatomy and severity of the coarctation as well as the size of mammary arteries, because these may be damaged by the saw. In the patient presented here, we decided to use the vibrating saw because the computerized tomography showed a very large mammary artery near the sternum.
Approximately 25 to 50 percent of patients with coarctation have bicuspid aortic valves, and these valves have a tendency to calcify in adult life, producing aortic stenosis . All of these lesions impose increased afterload on the left ventricle and, if severe and untreated, result in hypertrophy and failure of the left ventricle . This was the case for our patient upon admission to the hospital.
In adult patients with aortic coarctation in combination with other cardiac diseases, surgical management may be complicated, and there is no consensus on the optimal approach. The long-term outcome is known only after surgery and although stent therapy has been proven efficient, relatively simple and free adverse events in the majority of cases, the equivalence of the endovascular repair in the long-term has not yet been determined . Some authors have suggested a single-stage repair [6–8], while exposure of the descending aorta through a median sternotomy and the posterior pericardium was described by Vijayanagar et al  in a patient with aortic coarctation associated with aortic valve regurgitation. In that patient, the vascular graft was placed around the left margin of the heart and was anastomosed proximally to the anterior wall of the ascending aorta. Powell et al  described a modification of this technique in which the graft is routed around the right margin of the heart and anastomosed proximally to the right lateral ascending aorta. Routing the graft behind the inferior vena cava but anterior to the right inferior pulmonary vein may protect the graft if reoperation is necessary.
We conclude that adult patients with aortic coarctation combined with other cardiac pathologies may be treated with a single-stage repair. Because median sternotomy is the best approach, we believe that to minimize morbidity, a computerized tomography angiogram should be performed prior to surgery to identify possible aneurysmal dilatation of vessels involved in collateral circulation.
Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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