Literature DB >> 25596402

Hybrid treatment for thoracoabdominal aortic aneurysms in patients with Marfan syndrome.

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.
Copyright © 2015 Elsevier Inc. All rights reserved.

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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


  1 in total

Review 1.  Overview of current surgical strategies for aortic disease in patients with Marfan syndrome.

Authors:  Shunsuke Miyahara; Yutaka Okita
Journal:  Surg Today       Date:  2015-11-19       Impact factor: 2.549

  1 in total

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