Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Dilated right atrium"'
Publikováno v:
CASE : Cardiovascular Imaging Case Reports
Graphical abstract
Highlights • Isolated coronary sinus defect without persistent left superior vena cava is a rare cardiac defect. • Diagnosis can be difficult in the absence of other defects in an asymptomatic child. • Missed or difficul
Highlights • Isolated coronary sinus defect without persistent left superior vena cava is a rare cardiac defect. • Diagnosis can be difficult in the absence of other defects in an asymptomatic child. • Missed or difficul
Publikováno v:
Cardiology in the Young. 32:135-137
A Melody valve was successfully placed across a very stenotic right-sided component of a common atrioventricular valve because of ongoing troublesome arrhythmias in a young woman with an unbalanced atrioventricular septal defect, a very dilated right
Publikováno v:
JACC: Case Reports, Vol 3, Iss 4, Pp 594-596 (2021)
JACC Case Reports
JACC Case Reports
An acutely angulated coronary sinus ostium coupled with a dilated right atrium presents technical challenges for cardiac resynchronization therapy (CRT) implantation. Innovative use of a deployable left ventricle lead as an anchor to support guidewir
Autor:
S Balasubramanian
Publikováno v:
Journal of the Indian Academy of Echocardiography & Cardiovascular Imaging, Vol 4, Iss 2, Pp 217-219 (2020)
Aneurysms of the right atrium are extremely rare. These aneurysms can be associated with tachyarrhythmia, intracardiac thrombus formation, thromboembolism, and right ventricular compression precipitating heart failure. We report a case of a right atr
Publikováno v:
Asian Cardiovascular and Thoracic Annals. 26:563-565
A 17-year-old boy presented with facial puffiness and swelling in the lower limbs for 6 months and one episode of syncope 15 days earlier. Transthoracic echocardiography showed a dilated right atrium and right ventricle with right ventricular systoli
Autor:
Joanna Ganczar, Robert A. English
Publikováno v:
Annals of Pediatric Cardiology
Annals of Pediatric Cardiology, Vol 8, Iss 1, Pp 71-73 (2015)
Annals of Pediatric Cardiology, Vol 8, Iss 1, Pp 71-73 (2015)
We report a case of Uhl's anomaly in a 3-week-old infant that underwent central shunt placement, patent duct us arteriosus and main pulmonary artery ligation. The infant presented with room air saturation of 43%, dilated right ventricle with decrease
Autor:
Hiroaki Mano, Masayoshi Kofune, Kazumasa Sonoda, Toshiko Nakai, Yasuo Okumura, Koichi Nagashima, Kimie Ohkubo, Satoshi Kunimoto, Ichiro Watanabe, Tatsuya Kofune, Hironori Haruta, Atsushi Hirayama
Publikováno v:
Journal of Arrhythmia, Vol 29, Iss 4, Pp 238-241 (2013)
We describe a 49-year-old woman with atrial tachycardia (AT) and arrhythmogenic right ventricular cardiomyopathy/dysplasia. Cardiac magnetic resonance images showed a markedly dilated right atrium and right ventricle. Electroanatomical mapping showed
Publikováno v:
Pediatrics & Therapeutics.
The substrate for atrial fibrillation (AF) in young patients with congenital heart disease could be heterogeneous. We report a 24-year old patient with persistent AF having the dilated right atrium following surgical repair of congenital heart diseas
Publikováno v:
Indian Pacing and Electrophysiology Journal, Vol 12, Iss 1, Pp 15-18 (2012)
Indian Pacing and Electrophysiology Journal
Indian Pacing and Electrophysiology Journal
In this “featured arrhythmia” article we present a set of unusual intracardiac electrode tracings that were recorded in a patient with typical clockwise flutter but a very dilated right atrium. The potential mechanism underlying this phenomenon i
Publikováno v:
World journal for pediatriccongenital heart surgery. 7(4)
Giant right atrial aneurysm is a rare entity in infants and children. It needs to be distinguished from an atrial diverticulum, which can have similar presentation. Generally, an incidental finding in children, it can present with varied symptoms. We