| Literature DB >> 25596402 |
Maurizio Taurino1, Roberta Ficarelli2, Luigi Rizzo1, Nazzareno Stella1, Francesca Persiani1, Fabio Capuano3.
Abstract
Marfan syndrome is a heritable disorder of connective tissue leading to aortic aneurysms and other cardiovascular complications associated with reduced life expectancy. Although contemporary management of ascending aortic disease requires open surgical reconstruction, the combined retrograde visceral revascularization and endovascular exclusion (hybrid procedure) of entire thoracoabdominal aorta has been introduced for the management of descending thoracic and abdominal aortic pathology. The present experience reports 2 cases of thoracoabdominal aortic aneurysms, in Marfan patients, previously submitted to major cardiovascular surgical procedures, through a hybrid approach.Entities:
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Year: 2015 PMID: 25596402 DOI: 10.1016/j.avsg.2014.10.034
Source DB: PubMed Journal: Ann Vasc Surg ISSN: 0890-5096 Impact factor: 1.466