Literature DB >> 11500749

[Echocardiographic diagnosis of transposition of the great arteries associated with anomalous pulmonary venous connection].

L M Lopes1, G M Penha Tavares, F L Mailho, V P Cavalcante de Almeida , J A Mangione.   

Abstract

We report 2 cases of transposition of the great arteries associated with anomalous pulmonary venous connection emphasizing the clinical findings, the diagnosis, and the evolution of the association. One of the patients had the anomalous pulmonary venous connection in its total infradiaphragmatic form, in the portal system, and the other patient had a partial form, in which an anomalous connection of the left superior lobar vein with the innominate vein existed. At the time of hospital admission, the patients had cyanosis and respiratory distress with clinical findings suggesting transposition of the great arteries. The diagnosis in 1 of the cases, in which the anomalous connection was partial, was established only with echocardiography, without invasive procedures that would represent risk for the patient; in the other case, in which the anomalous connection was total, the malformation was only evidenced with catheterization. The patients underwent surgery for anatomical correction of the heart disease. Only 1 patient had a good outcome.

Entities:  

Mesh:

Year:  2001        PMID: 11500749     DOI: 10.1590/s0066-782x2001000700007

Source DB:  PubMed          Journal:  Arq Bras Cardiol        ISSN: 0066-782X            Impact factor:   2.000


  2 in total

1.  Transposition of the great arteries with total anomalous pulmonary venous connection in a 1½year-old child: Pulmonary arterial hypertension - An advantage.

Authors:  Rose Okwunu Abah; Atul Prabhu; Ashish Katewa; Balswaroop Sahu
Journal:  Ann Pediatr Cardiol       Date:  2021-02-16

2.  Unusual association of transposition of great arteries with infradiaphragmatic pulmonary venous return.

Authors:  Giuseppe Scrascia; Anna Maria Pia Grimaldi; Dario Troise; Gabriele Scalzo
Journal:  Ann Pediatr Cardiol       Date:  2019-12-04
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.