scholarly journals Giant right atrial aneurysm

2018 ◽  
Vol 28 (4) ◽  
pp. 645-646 ◽  
Author(s):  
Aisling Kinsella ◽  
Jagdish Butany ◽  
Bernd J Wintersperger ◽  
Christopher Feindel
2000 ◽  
Vol 48 (1) ◽  
pp. 35-37 ◽  
Author(s):  
M. Suedkamp ◽  
M. Horst ◽  
U. Mehlhorn ◽  
U. Hoppe ◽  
G. Arnold ◽  
...  

2017 ◽  
Vol 29 (1) ◽  
pp. 23-26
Author(s):  
Fatoş ALKAN ◽  
Özgür BAYTURAN ◽  
Mecnun ÇETİN ◽  
Şenol COŞKUN

2018 ◽  
Vol 2018 ◽  
pp. 1-3
Author(s):  
Ayse Sulu ◽  
Osman Baspinar ◽  
Selim Kervancıoglu ◽  
Samil Hizli

Right atrial aneurysms were first described in 1955, and subsequently, only a few cases have been reported. The etiology of this condition is unknown. Its comorbidity with cholestasis has not previously been reported in the literature. An 11-month-old baby female, who was an offspring from a first-cousin marriage, was referred to our hospital for investigation of jaundice. She underwent echocardiography because of a heart murmur, and this revealed a giant right atrial aneurysm. In addition, her liver biopsy confirmed the diagnosis of progressive familial intrahepatic cholestasis (PFIC) type 3. Although both conditions are rare, we found their comorbidity interesting and are thus reporting the case.


2015 ◽  
Vol 10 (1) ◽  
Author(s):  
Karolis Jonavicius ◽  
Arturas Lipnevicius ◽  
Rita Sudikiene ◽  
Edvardas Zurauskas ◽  
Virgilijus Lebetkevicius ◽  
...  

2008 ◽  
Vol 129 (1) ◽  
pp. e5-e6 ◽  
Author(s):  
John Papagiannis ◽  
Andrew Chatzis ◽  
George Sarris

2012 ◽  
Vol 64 (2) ◽  
pp. 200-202 ◽  
Author(s):  
V.S. Narain ◽  
Aniket Puri ◽  
R. Sethi ◽  
Pallavi Aga ◽  
Suresh Behera ◽  
...  

2001 ◽  
Vol 9 (3) ◽  
pp. 226-228
Author(s):  
Yavuz Beşoğul ◽  
Bülent Tünerir ◽  
Celal Kirdar ◽  
Bilgin Timuralp ◽  
Recep Aslan

2016 ◽  
Vol 9 (4) ◽  
pp. 459-462 ◽  
Author(s):  
Laurynas Bezuska ◽  
Frances A. Bu’Lock ◽  
Robert H. Anderson ◽  
Simone Speggiorin ◽  
Antonio F. Corno

Giant congenital right atrial aneurysms are rare, with their natural history complicated by death, heart failure, arrhythmias, and thrombosis. Prenatal diagnosis of the defect is feasible and allows an early preparation of a plan for management. We present details of a patient diagnosed prenatally with a giant right atrial aneurysm, which was successfully treated surgically as soon as the patient became symptomatic.


2016 ◽  
Vol 65 (7) ◽  
pp. 404-407
Author(s):  
Sanae Yamauchi ◽  
Yasuyuki Suzuki ◽  
Kazuyuki Daitoku ◽  
Masaomi Kimura ◽  
Ken Okumura ◽  
...  

2015 ◽  
Vol 18 (2) ◽  
pp. 66
Author(s):  
I. A. Shelestova ◽  
Ye. D. Kosmacheva ◽  
V. A. Porkhanov ◽  
N. V. Soroka

In this paper, we describe the case of a giant right atrial aneurysm in a 78-year old patient with atrial fibrillation diagnosed during echocardiography.


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