Congenitally corrected transposition and mitral atresia complicated by restrictive atrial septum.


Journal

Journal of clinical ultrasound : JCU
ISSN: 1097-0096
Titre abrégé: J Clin Ultrasound
Pays: United States
ID NLM: 0401663

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 15 05 2019
revised: 26 05 2020
accepted: 04 07 2020
pubmed: 5 8 2020
medline: 25 2 2021
entrez: 5 8 2020
Statut: ppublish

Résumé

Congenitally corrected transposition (ccTGA), also known as L-transposition of the great arteries (L-TGA), is a rare cardiac malformation accounting for approximately 0.05% of congenital heart disease, characterized by ventricular inversion, discordant ventriculo-arterial connections with a normal visceroatrial relationship. It was first described by Baron Rokitansky in 1875, and prenatal sonographic diagnosis can be difficult. Symptomatology and clinical presentation of this malformation are related to the associated intracardiac defects. We report a rare case of severe, complex cardiac disease: prenatally diagnosed ccTGA with atrial restriction, mitral atresia, Ebsteinoid tricuspid valve, and severe pulmonary valve stenosis, who subsequently developed left pulmonary vein stenosis.

Identifiants

pubmed: 32748445
doi: 10.1002/jcu.22897
doi:

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

510-512

Informations de copyright

© 2020 Wiley Periodicals LLC.

Références

Wallis GA, Debich-Spicher D, Anderson RH. Congenitally corrected transposition. Orphanet J Rare Dis. 2011;6:22.
Prieto LR, Hordof AJ, Secic M, et al. Progressive tricuspid valve disease in patients with congenitally corrected transposition of the great arteries. Circulation. 2018;98:997.
Santoro G, Masiello P, Baldi C, et al. Corrected transposition of the great arteries with isolated aortic coarctation: in utero echocardiographic diagnosis. Pediatr Cardiol. 1997;18:396.
Lowenthal A, Kipps AK, Brook MM, et al. Prenatal diagnosis of atrial restriction in hypoplastic left heart syndrome is associated with decreased 2-year survival. Prenat Diagn. 2012;32:485.
Divanovic A, Hor K, Cnota J, et al. Prediction and perinatal management of severely restrictive atrial septum in fetuses with critical left heart obstruction: clinical experience using pulmonary venous Doppler analysis. J Thorac Cardiovasc Surg. 2011;141988:.988-994.
Karl TR. The role of the Fontan operation in the treatment of congenitally corrected transposition of the great arteries. Ann Pediatr Cardiol. 2011;4:103.

Auteurs

Sarah Pradhan (S)

The Congenital Heart Collaborative, Rainbow Babies and Children's Hospital, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.

James Strainic (J)

The Congenital Heart Collaborative, Rainbow Babies and Children's Hospital, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.

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