Results 151 to 160 of about 724 (165)
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Herz, 2011
A 58-year-old male was referred for catheter ablation for atrial fibrillation. He was incidentally diagnosed with cor triatriatum sinister by preoperative transesophageal echocardiography and cardiovascular computed tomography. The patient has since been free from atrial fibrillation for over 24 months following successful electrical pulmonary vein ...
K, Fukumoto +9 more
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A 58-year-old male was referred for catheter ablation for atrial fibrillation. He was incidentally diagnosed with cor triatriatum sinister by preoperative transesophageal echocardiography and cardiovascular computed tomography. The patient has since been free from atrial fibrillation for over 24 months following successful electrical pulmonary vein ...
K, Fukumoto +9 more
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Prenatal diagnosis of cor triatriatum sinister
Ultrasound in Obstetrics & Gynecology, 2023Y. Matsubara +3 more
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Surgical correction of cor triatriatum sinister in a kitten
Journal of the American Animal Hospital Association, 1998A seven-month-old, male domestic shorthair was presented for respiratory distress. Cor triatriatum sinister was diagnosed based on echocardiography. Surgical dilatation and tearing of the anomalous membrane dividing the left atrium resulted in resolution of clinical signs. Intraoperative echocardiography was used to evaluate the adequacy of the repair.
K W, Wander, E, Monnet, E C, Orton
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COR TRIATRIATUM SINISTER: A SILENT THREAT
European Heart Journal SupplementsAbstract We present the clinical case of a 22–year–old man practicing competitive sport (sprinter) who underwent an echocardiogram in asymptomatic condition. The patient appeared to be in good health. No previous medical history. No cardiovascular risk factors. Echocardiogram revealed good biventricular function and no valvular diseases;
M Russo, D Zaffalon, F De Conti
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Multimodality Imaging of Cor Triatriatum Sinister in an Octagenerian
Echocardiography, 2014Cor triatriatum sinister (CTS) is a rare congenital cardiac anomaly in which a fibromuscular membrane divides the atrium into two chambers. As CTS can occur as an isolated anomaly, it is frequently associated with other cardiac anomalies. Although symptoms are usually encountered in infancy, CTS may rarely present in adulthood when the membrane ...
Tahir, Bezgin +6 more
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Cor triatriatum sinister--three case reports.
Medicinski arhiv, 2010Cor triatriatum is a rare congenital heart disease (0.1% of all congenital cardiac defects), but a higher incidence, up to 0.4% has been reported in autopsies of pts with CHD (1, 2, 7). There are two types: left and right. Cor triatriatum sinister is more common that dexter. Cor triatriatum dextrum is extremely rare.
Myrvete, Kelmendi +3 more
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Obstructed Supramitral Inflow: Cor Triatriatum Sinister Presentation in Adulthood
Journal of Cardiothoracic and Vascular AnesthesiaCor triatriatum is a rare congenital heart defect that occurs when a fibromuscular membrane divides the atrium into two chambers, which may impair blood flow to the ventricle. When it does, the symptoms usually manifest during infancy or early childhood.
Sara Medellin +2 more
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Cor triatriatum sinister: echocardiographic assessment.
Puerto Rico health sciences journal, 1990A 16 year old white female presented with paroxysmal cough and hemoptysis of recent onset. Cardiac evaluation was consistent with pulmonary hypertension. Cor triatriatum sinister was diagnosed by echocardiography. The clinical presentation and the echocardiographic features of this anomaly are discussed.
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Atrioventricular septal defect with cor triatriatum sinister.
Chang Gung medical journal, 2007Cor triatriatum (CT) is a rare cardiac anomaly, characterized by a membrane in the left atrium which separates the atrium into the proximal and distal chambers. Association of CT with atrioventricular septal defects (AVSD) is extremely rare; only three cases with complete AVSD and 10 with partial AVSD have been reported. In this study, we present an 11-
Yu-Yin, Liu +6 more
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