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J Thorac Cardiovasc Surg 1994;107:1469-1471
© 1994 Mosby, Inc.
SURGERY FOR ACQUIRED HEART DISEASE |
Nieuwegein, The Netherlands
From the Department of Cardiothoracic Surgery, St. Antonius Hospital, Nieuwegein, The Netherlands.
Received for publication April 24, 1991. Accepted for publication Oct. 5, 1993. Address for reprints: Michel W. Verkroost, MD, St. Antonius Hospital, P.O. Box 2500, 3430 EM, Nieuwegein, The Netherlands.
Abstract
An aneurysmal origin of an aberrant right subclavian artery should preferably be closed with a prosthetic patch inserted with the aid of cardiopulmonary bypass with deep hypothermia and circulatory arrest. Three patients were operated on: a transaortic approach was used in two and a transaneurysmal approach in one. This technique allows a single-stage surgical correction of this rare anomaly through a median sternotomy and obviates the need for hazardous and difficult side clamping of the aorta. (J THORAC CARDIOVASC SURG 1994;107:1469-71)
Several types of congenital vascular anomalies produce partial or total encirclement of the trachea and esophagus. These vascular rings, slings, and other abnormalities of the aortic arch rather frequently lead to dysphagia or dyspnea with stridor, or both.
A left-sided aortic arch with an aberrant right subclavian artery, as first described by Hunauld,
1 is the most common aortic arch anomaly, occurring in approximately 0.5% of the population.
2 The second most common aortic arch anomaly is caused by persistence of both the right (posterior) and left (anterior) fourth branchial arches. The majority of patients with this anomaly have anatomic continuity but luminal atresia of the anterior arch.
Aneurysms in the course of an aberrant right subclavian artery are not frequently encountered.
3 Between 1956 and 1990 only 39 cases were reported.
4,5 An aneurysm at the very origin of an aberrant right subclavian artery is rare, with only four cases reported until now.
6-9 In the St. Antonius Hospital, in a 6-year period, we have operated on three patients with this latter combination of anomalies. To our belief repair of this rare entity necessitates a specific surgical technique of patch closure with the aid of deep hypothermia and circulatory arrest.
METHODS AND RESULTS
In our three patients a mass was visible in the upper part of the mediastinum on the chest x-ray films. Computed tomographic scans of the mediastinum and intraarterial angiograms revealed a large aneurysm at the origin of an aberrant right subclavian artery in two patients (both 68 years of age) (Fig. 1) and a double aortic arch with atresia of the anterior arch and a large aneurysm originating from the dorsal aortic arch in the third patient (47 years of age). The first two patients had dysphagia, and the third had progressive swelling of the head and neck because the aneurysm was compressing the superior vena cava.
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In children the aberrant right subclavian artery is soft and pliable, whereas by late adolescence the development of atherosclerotic rigidity, tortuosity, and dilation of its origin may result in compression of the esophagus or superior vena cava, as occurred in our three patients.
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The surgical approach in four patients with an aneurysmal origin of an aberrant right subclavian artery so far described in the literature consisted of the following: a left thoracotomy in two patients (one in combination with a right supraclavicular incision), a right thoracotomy in one patient,
6-8 and in the fourth patient a technique similar to the one that we described, namely, median sternotomy with a transaortic approach to the aneurysm with deep hypothermia and circulatory arrest.
9 In the fourth patient the operation was combined with myocardial revascularization.
We used a one-stage approach through a median sternotomy with deep hypothermia and circulatory arrest to facilitate a good exposure of the orifices of the aneurysm, either transaortically or through the aneurysm. Such an approach also obviates the need for difficult and hazardous clamping of the aorta around the base of the aneurysm, which is likely to be calcified in these generally older patients. In addition, the (peri)aneurysmal aortic tissue is frequently fragile. Extension of the incision into the right supraclavicular region adequately exposes the distal right subclavian artery and facilitates restoration of its circulation by insertion of an interposition graft that can be anastomosed to the ascending aorta or the right common carotid artery.
Profound hypothermia with circulatory arrest is the most common method of cerebral protection during operations on the aortic arch. Alternatively, as we currently favor, selective cold cerebral perfusion by cannulation of one or both carotid arteries with profound corporeal hypothermia and circulatory arrest can be performed. The latter technique may be safer in older patients or in complex arch operations with expected long arrest times. Another alternative for cerebral protection with cold cerebroplegia was recently described by Bachet and associates.
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References
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