Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros

Base de dados
Tipo de documento
País de afiliação
Intervalo de ano de publicação
1.
J Imaging ; 8(10)2022 Oct 14.
Artigo em Inglês | MEDLINE | ID: mdl-36286374

RESUMO

Ascending thoracic aortic aneurysm is a life-threatening disease, which is difficult to detect prior to the occurrence of a catastrophe. Epidemiology patterns of ascending thoracic aortic dilations/aneurysms remain understudied, whereas the risk assessment of it may be improved. The electronic databases PubMed/Medline 1966-2022, Web of Science 1975-2022, Scopus 1975-2022, and RSCI 1994-2022 were searched. The current guidelines recommend a purely aortic diameter-based assessment of the thoracic aortic aneurysm risk, but over 80% of the ascending aorta dissections occur at a size that is lower than the recommended threshold of 55 mm. Moreover, a 55 mm diameter criterion could exclude a vast majority (up to 99%) of the patients from preventive surgery. The authors review several visualization-based and alternative approaches which are proposed to better predict the risk of dissection in patients with borderline dilated thoracic aorta. The imaging-based assessments of the biomechanical aortic properties, the Young's elastic modulus, the Windkessel function, compliance, distensibility, wall shear stress, pulse wave velocity, and some other parameters have been proposed to improve the risk assessment in patients with ascending thoracic aortic aneurysm. While the authors do not argue for shifting the diameter threshold to the left, they emphasize the need for more personalized solutions that integrate the imaging data with the patient's genotypes and phenotypes in this heterogeneous pathology.

2.
Eur J Cardiothorac Surg ; 58(1): 196-198, 2020 07 01.
Artigo em Inglês | MEDLINE | ID: mdl-31860063

RESUMO

We present a case of a 42-year-old male patient with severe supravalvular aortic stenosis associated with aortic and mitral valve stenosis as well as an anomalous origin of the right coronary ostium caused by deletion in the q11.23 region of the human chromosome 7 in a patient with Williams-Beuren syndrome.


Assuntos
Estenose Aórtica Supravalvular , Anormalidades Cardiovasculares , Síndrome de Williams , Adulto , Estenose Aórtica Supravalvular/diagnóstico por imagem , Estenose Aórtica Supravalvular/etiologia , Estenose Aórtica Supravalvular/cirurgia , Humanos , Masculino
3.
Interact Cardiovasc Thorac Surg ; 22(6): 854-5, 2016 06.
Artigo em Inglês | MEDLINE | ID: mdl-26921885

RESUMO

This clinical case demonstrates a successful simultaneous approach for Type B aortic dissection in association with Kommerell's diverticulum using an E-vita OPEN PLUS Hybrid prosthesis. Computed tomography in the early postoperative period and after a 6-month follow-up showed favourable surgical outcomes.


Assuntos
Aorta Torácica/cirurgia , Aneurisma da Aorta Torácica/cirurgia , Dissecção Aórtica/cirurgia , Implante de Prótese Vascular/métodos , Divertículo/cirurgia , Artéria Subclávia/anormalidades , Dissecção Aórtica/complicações , Aneurisma da Aorta Torácica/etiologia , Divertículo/complicações , Humanos , Masculino , Pessoa de Meia-Idade , Artéria Subclávia/cirurgia , Tomografia Computadorizada por Raios X
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA