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Large aortic aneurysm and dissection in a patient with Marfan’s syndrome
Pivatto Júnior, Fernando; Ramos, Leila Denise Cardoso; Foppa, Murilo; Torres, Felipe Soares.
  • Pivatto Júnior, Fernando; Hospital de Clínicas de Porto Alegre. Serviço de Cardiologia. Porto Alegre. BR
  • Ramos, Leila Denise Cardoso; Hospital de Clínicas de Porto Alegre. Serviço de Cardiologia. Porto Alegre. BR
  • Foppa, Murilo; Hospital de Clínicas de Porto Alegre. Serviço de Cardiologia. Porto Alegre. BR
  • Torres, Felipe Soares; Hospital de Clínicas de Porto Alegre. Departmento de Radiologia. Porto Alegre. BR
Clin. biomed. res ; 35(2): 112-115, 2015. ilus
Article in English | LILACS | ID: lil-780246
ABSTRACT
Marfan’s syndrome is an autosomal dominant disorder of connective tissue affecting approximately 1 in 5000 people. In individuals with this syndrome, more than 90% of deaths from known causes result from cardiovascular complications, such as aortic dissection, aortic regurgitation, and congestive cardiac failure. In this report, we present a patient with a large symptomatic aortic aneurysm and chronic dissection, severe aortic regurgitation and cardiomegaly, treated successfully with resection of the proximal aorta and placement of a mechanic aortic valved graft...
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Full text: Available Index: LILACS (Americas) Main subject: Aortic Aneurysm / Aortic Dissection / Marfan Syndrome Limits: Humans Language: English Journal: Clin. biomed. res Journal subject: Medicine Year: 2015 Type: Article Affiliation country: Brazil Institution/Affiliation country: Hospital de Clínicas de Porto Alegre/BR

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Full text: Available Index: LILACS (Americas) Main subject: Aortic Aneurysm / Aortic Dissection / Marfan Syndrome Limits: Humans Language: English Journal: Clin. biomed. res Journal subject: Medicine Year: 2015 Type: Article Affiliation country: Brazil Institution/Affiliation country: Hospital de Clínicas de Porto Alegre/BR