| Literature DB >> 25120397 |
Petar M Vukovic1, Dragana Kosevic1, Miroslav Milicic1, Ljiljana Jovovic1, Ivan Stojanovic1, Slobodan Micovic1.
Abstract
Cor triatriatum dexter is a rare congenital heart anomaly in which a membrane divides the right atrium into 2 chambers. We report the case of a 43-year-old woman who had cor triatriatum dexter and a large atrial septal defect. During attempted percutaneous closure, the balloon disrupted the membrane and revealed that the defect had no inferior rim, precluding secure placement of an Amplatzer Septal Occluder. Surgical treatment subsequently proved to be successful. In patients with an incomplete membrane and a septal defect with well-defined rims, percutaneous treatment can be the first choice. In patients who have cor triatriatum dexter and unfavorable anatomic features or concomitant complex heart anomalies, open-heart surgery remains the gold standard for treatment.Entities:
Keywords: Abnormalities, multiple; cor triatriatum/complications/surgery; heart atria/pathology; heart defects, congenital/diagnosis; heart septal defects, atrial; treatment outcome
Mesh:
Year: 2014 PMID: 25120397 PMCID: PMC4120507 DOI: 10.14503/THIJ-13-3366
Source DB: PubMed Journal: Tex Heart Inst J ISSN: 0730-2347