| Literature DB >> 29152268 |
Hossein Sate1, Najmeh Reshadati1, Parvaneh Aliakbarzadeh1, Negin Molazadeh1.
Abstract
Right atrial appendage aneurysm (RAAA) is rarely encountered with variable intracardiac anatomy. We report a case of asymptomatic RAAA in a patient with dextrocardia and anomalous origin of RCA from left coronary sinus which was treated successfully by CABG and the aneurysm was completely excised.Entities:
Keywords: Atrial appendage aneurysm; dextrocardia; echocardiography
Year: 2017 PMID: 29152268 PMCID: PMC5676291 DOI: 10.1002/ccr3.1150
Source DB: PubMed Journal: Clin Case Rep ISSN: 2050-0904
Figure 1Electrocardiogram showing acute ST elevation myocardial infarction.
Figure 2Chest X‐ray (posterior anterior view) of a 53‐year‐old man showing dextrocardia, with the cardiac apex pointing to the right.
Figure 3CAG findings indicating subtotal lesion in LAD and 50% stenosis in LM and LCX along with abnormal origin of RCA from left coronary sinus without significant lesion.
Figure 4(A) Transthoracic echocardiography from apical four‐chamber view demonstrating a large echo‐free cavity lateral of right ventricle with anticontrast inside it and compressive of RV and contiguous with main body of right atrium. (B) Transesophageal echocardiography showed a right atrial appendage aneurysm and atrial structures. Contrast study showed better visualization of RAA and its connection with RA. (C) Transesophageal echocardiography demonstrating combination of dextrocardia and RAAA.