Results 31 to 40 of about 1,273 (168)

Case report: The impact of percutaneous atrial septal defect closure in pulmonary hypertension with co-existing cor triatriatum sinister and multiple cardiac comorbidities

Frontiers in Cardiovascular Medicine, 2022
Cor triatriatum sinister is a rare congenital anomaly characterized by the left-sided triatrial form of the heart. Diverse theories have been proposed regarding its formation, and the failure of incorporation of the common pulmonary vein into the left ...
I-Hsin Tai, I-Hsin Tai, I-Hsin Tai, Tsung-Cheng Shyu, Tsung-Cheng Shyu, Tsung-Cheng Shyu, Kai-Sheng Hsieh, Kai-Sheng Hsieh, Kai-Sheng Hsieh, Ke-Wei Chen, Ke-Wei Chen, Wan-Jane Tsai, Kuo-Yang Wang, Kuo-Yang Wang, Kuo-Yang Wang   +14 more
doaj   +1 more source

A Case of Acquired Cor Triatriatum Dextrum

Journal of the Indian Academy of Echocardiography & Cardiovascular Imaging
Cor triatriatum is a rare congenital heart condition, with cor triatriatum sinistrum being more common than cor triatriatum dextrum. Most patients are asymptomatic, but some may experience symptoms due to inflow obstruction.
M. Haashim, M. Nandakumaran, G. Prathap Kumar, D. Rajasekhar Ramesh   +3 more
doaj   +1 more source

Cor Triatriatum: Case Report of Emergency Department Diagnosis

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, Asalim Thabet, Rebecca Blue, Tyler Greenfield   +3 more
doaj   +1 more source

A Rare Cause of Pulmonary Hypertension in a 4-Year-Old Toddler: Association of Cor Triatriatum Sinister and Pulmonary Arteriovenous Malformation

Case Reports in Pediatrics, 2020
Cor triatriatum sinister is a rare congenital cardiac anomaly. The anomaly is caused by a fibromuscular membrane that divides the left atrium into two cavities.
Can Yilmaz Yozgat, Erkan Cakir, Hakan Yazan, Hafize Otcu Temur, Kahraman Yakut, Yilmaz Yozgat   +5 more
doaj   +1 more source

Transcatheter Closure of Atrial Septal Defect in a Patient with Cor Triatriatum Sinister and Atrial Septal Defect

Case Reports in Cardiology, 2011
Cor triatriatum sinister is a rare congenital heart disease and rarely found in adults. The authors describe an asymptomatic 20-year old man presenting with heart murmur by check up.
Wasana Hongkan, Kriangsak Thongchaiprasit, Kritvikrom Durongpisitkul   +2 more
doaj   +1 more source

Cor triatriatum presenting as heart failure with reduced ejection fraction: a case report

Journal of Cardiothoracic Surgery, 2011
Cor triatriatum is a rare congenital cardiac malformation and it usually refers to the left atrium. We report an unusual case of cor triatriatum in a 33 - year old woman presented with congestive heart failure caused by left ventricular systolic ...
Prapa Efi, Kratimenos Theodoros, Nenekidis Ioannis, Paralikas Ioannis, Almpanis George, Anagnostakou Vania, Kokotsakis John, Tragotsalou Nikolitsa, Lioulias Achilleas, Mazarakis Andreas   +9 more
doaj   +1 more source

A Rare Congenital Heart Disease in an Elderly Long-Distance Runner: A Case Report

Case Reports in Cardiology, 2012
Introduction. Cor triatriatum is a rare congenital heart disease found incidentally in children. Although cor triatriatum can be an incidental finding in asymptomatic adults; it is extremely rare to find elderly patients without symptoms and is unique in
K. R. Bhamidipati, N. C. Shah, M. C. Connaughton   +2 more
doaj   +1 more source

A six-chambered heart: cor triatriatum sinister with double-chambered right ventricle in association with ventricular septal defect

The Egyptian Heart Journal, 2022
Background Cor triatriatum has been described as a heart with three atria in which the left atrium (cor triatriatum sinistrum) or right atrium (cor triatriatum dextrum) is divided into two compartments by a fold of tissue, a membrane, or a fibromuscular ...
Vivek Jaswal, Pratyaksha Rana, Vidur Bansal, Krishna Prasad Gourav, Arun Sharma, Shyam Kumar Singh Thingnam   +5 more
doaj   +1 more source

Fetal Diagnosis of Hypoplastic Left Heart Syndrome With Restrictive Atrial Septum—Atrial Septal Morphology, Associated Lung Disease and Outcomes

Prenatal Diagnosis, Volume 46, Issue 2, Page 183-192, February 2026.
ABSTRACT Objective Fetuses with hypoplastic left heart syndrome (HLHS) and restrictive/intact atrial septum (RAS) have high mortality, partly due to pulmonary lymphangiectasia (PL). This study aimed to characterize atrial septal morphology in fetuses with HLHS and RAS and evaluate the impact of fetal intervention on PL and outcomes.
Sofie Dannesbo, Gloria Ho, Mike Seed, Vitor Guerra, Rajiv Chaturvedi, Andrew C. Cook, Niels Vejlstrup, Kasper Iversen, Henning Bundgaard, Lindsay R. Freud   +9 more
wiley   +1 more source

Chylothorax after patent ductus arteriosus ligation in a dog with persistent left cranial vena cava

Australian Veterinary Journal, Volume 103, Issue 12, Page 919-922, December 2025.
This report is the first to document chylothorax after patent ductus arteriosus (PDA) ligation in a dog with a persistent left cranial vena cava (PLCVC), highlighting potential complications arising from concurrent cardiovascular anomalies. A nine‐month‐old female desexed Pomeranian was referred for PDA. Echocardiography confirmed a left‐to‐right shunt
TR Nash, GL Hosgood
wiley   +1 more source