Results 21 to 30 of about 221,247 (223)
Percutaneous Closure of Patent Foramen Ovale in a Patient With Incomplete Cor Triatriatum Sinister: A Case Report. [PDF]
J Clin UltrasoundWe present the case of a 55‐year‐old male who experienced a cryptogenic ischemic stroke, likely due to a patent foramen ovale (PFO) in the setting of an incomplete cor triatriatum sinister (CTS) and a 30 mm GORE Cardioform Septal Occluder was successfully implanted.
Apostolos A +8 more
europepmc +2 more sources
Cor triatriatum sinister: a case series
Türk Kardiyoloji Derneği Arşivi, 2016 Objective: As a highly rare congenital defect, cor triatriatum sinister represents only 0.1% of congenital cardiac anomalies. Depending on the degree of obstruction and the accompanying symptoms, cor triatriatum can be diagnosed at any age.
Onur Isik +4 more
doaj +2 more sources
Residual cor triatriatum sinistrum after atrial septal defect repair in an adult [PDF]
Journal of Cardiothoracic SurgeryCor triatriatum sinistrum is an uncommon congenital heart disease. The surgical repair outcomes are often satisfactory without reintervention. We report a case of residual cor triatriatum sinistrum after atrial septal defect repair in an adult.
YangBo Yan, Jia Hu, ChangPing Gan
doaj +2 more sources
Brazilian Journal of Cardiovascular Surgery, 2003 The association between total anomalous pulmonary venous connection and cor triatriatum is extremely rare. We emphasize the possibility of rupturing the membrane of cor triatriatum in the preoperative cineangiographic study, providing a significant ...
Ulisses Alexandre Croti +3 more
doaj +2 more sources
Clinical Case Reports, 2018 Key Clinical Message Cor triatriatum dexter (CTD) is an extremely rare finding (
Dominika Zoltowska +1 more
doaj +3 more sources
Wong's anomaly – A rare variant of cor triatriatum [PDF]
Indian Heart Journal, 2015 Cor triatriatum sinistrum is an extremely rare congenital heart disease. It is even more uncommon in adults, and clinically significant mitral valve lesion complicating cor triatriatum is distinctly rare.
K. Jayaprakash +5 more
doaj +2 more sources
Cor Triatriatum: Case Report of Emergency Department Diagnosis [PDF]
Clinical Practice and Cases in Emergency Medicine, 2018 Cor triatriatum is a rare, congenital heart defect. When diagnosis does not occur in infancy, primary symptoms in an older patient may mimic reactive airway disease. We report a case of cor triatriatum in an older child, previously diagnosed with asthma,
Camille Halfman +3 more
doaj +2 more sources
CJC Pediatric &Congenital Heart Disease, Volume 3, Issue 4, Page 137-140, August 2024.Cor triatriatum dexter is a rare but benign congenital heart abnormality where the right atrium is septated due to a prominent eustachian valve.1,2 The eustachian valve is an embryologic structure that lies at the junction of the inferior vena cava and protrudes into the inferior right atrial cavity.
Abdulmajeed Alotay +3 more
wiley +2 more sources
COR TRIATRIATUM DEXTER EN LA EDAD ADULTA / Cor triatriatum dexter in adulthood [PDF]
CorSalud, 2013 Resumen: El cor triatriatum dexter es una malformación muy rara, en el cual la aurícula derecha está dividida en dos cámaras por un tabique. Se presenta el caso de una joven de 24 años de edad con antecedentes de insuficiencia cardíaca por miocardiopatía
Aliet Arrué Guerrero +2 more
doaj +1 more source
Arquivos Brasileiros de Cardiologia, 2017 Um homem de 25 anos apresentou-se a clinica com queixas de palpitacoes. O ecocardiograma transtoracico (ETE) mostrou presenca de membrana no atrio esquerdo sugestiva de cor triatriatum (coracao triatrial) []. Esse achado foi confirmado com ecocardiograma transesofagico (ETE), que revelou uma membrana no atrio esquerdo que se fixa na crista de Coumadin ...
Hitesh Raheja +4 more
doaj +3 more sources