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J Thorac Cardiovasc Surg 2007;134:1055-1057
© 2007 The American Association for Thoracic Surgery
Brief Communication |
a Department of Cardiothoracic Surgery, Juan Canalejo Hospital, A Coruña, Spain
b Department of Interventional Radiology, Juan Canalejo Hospital, A Coruña, Spain.
Received for publication June 3, 2007; accepted for publication June 21, 2007. * Address for reprints: Victor X. Mosquera, MD, Cardiac Surgery Department, Hospital Juan Canalejo, As Xubias n°84, CP 15006, A Coruña, Spain. (Email: vxmr{at}canalejo.org; vxmr{at}yahoo.es).
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Although an aberrant right subclavian artery (ARSA) is the most common abnormality of aortic arch development, it is an unusual entity to encounter associated with thoracic aortic dissection. We report the successful endovascular treatment of this association in a critically ill patient.
An 80-year-old man was referred to our institution with the diagnosis of an acute aortic Stanford type B dissection (Figure 1, A). The computed tomographic scan images also showed a thoracoabdominal aortic aneurysm extending from an ARSA (Figure 1, B) to the esophageal hiatus (Crawford type I).
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Because of the patients critical status and high surgical risk, emergency endovascular treatment was indicated. Notwithstanding, the procedure was technically demanding, because the endograft had to be deployed while avoiding occlusion of the ARSA. However, the diameter of the aortic aneurysm distal to the origin of the ARSA was greater than 46 mm, which is the maximum diameter amenable for the standard Medtronic Valiant thoracic endograft (Medtronic, Inc, Santa Rosa, Calif). Therefore, the deployment of the endoprosthesis was adjusted to the origin of the ARSA, where the thoracic aneurysm had a neck of 42 mm. A Valiant endograft, 160 mm in length and 46 mm in diameter, was deployed at the level of ARSA origin, so that its floppy FreeFlo straight portion (Figure 2, A), which is fenestrated, allowed blood flow through the artery. In this way, the flow through the aberrant artery was preserved (control computed tomographic scans, Figure 2, A and B).
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Aberrant subclavian artery, also called arteria lusoria, was first described by Bayford in 1794. It is the most common form of aortic arch anomaly and has a reported incidence of 0.5% to 2%. It results from regression of the right fourth aortic arch between the carotid and subclavian arteries.1
The association of aortic dissection and ARSA is rarely encountered; however, it has very important implications in treatment, either surgical or endovascular. A number of surgical techniques have been proposed for treatment of this pathologic condition. These include transposition or bypass of the distal portion of the aberrant artery into the adjacent carotid artery, resection of the origin of the aneurysm from the descending thoracic aorta, and repair of the aortic dissection/aneurysm with the elephant trunk technique.2
The use of partial or total cardiopulmonary bypass, hypothermia, and circulatory arrest is normally necessary. Nevertheless, endovascular therapy has revolutionized this surgery. Complex open surgical procedures may be replaced by endovascular treatment, which is associated with a lower perioperative morbidity and mortality.3
In this case, the very high surgical risk of the patient led us to choose an endovascular treatment. We decided to use the Valiant system, which is a third-generation endoprosthesis designed specifically for the exclusion of thoracic aortic disease.4
Its floppy FreeFlo straight portion allowed us to deploy the endograft without occluding the ARSA and, therefore, without compromising either the right arm blood supply or the right vertebral artery flow.
References
This article has been cited by other articles:
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V. X. Mosquera, J. M. Herrera, M. Marini, F. Estevez, I. Cao, D. Gulias, J. V. Valle, and J. J. Cuenca Mid-term results of thoracic endovascular aortic repair in surgical high-risk patients Interact CardioVasc Thorac Surg, July 1, 2009; 9(1): 61 - 65. [Abstract] [Full Text] [PDF] |
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