[Retracted Article] Congenital Left Atrial Appendage Aneurysm:A Case Report

Hanieh Bazrafshan; Alireza  Moaref; Amirhossein Salimi; Reza Fakhar; Shirin Sarejloo; Abdolali Zolghadrasli

International Cardiovascular Research Journal

The Official Annually Journal of Cardiovascular Research Center, Shiraz University of Medical Sciences

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[Retracted Article] Congenital Left Atrial Appendage Aneurysm:A Case Report

Author(s):

Hanieh Bazrafshan

^1,*,

Alireza Moaref²,

Amirhossein Salimi³,

Reza Fakhar⁴,

Shirin Sarejloo²,

Abdolali Zolghadrasli²

1Clinical Neurology Research Center, Department of Neurology, Shiraz University of Medical Sciences, Shiraz, IR Iran

2Cardiovascular Research Center, Shiraz University of Medical Sciences, Shiraz, IR Iran

3Student Research Committee, Shahid Sadoughi University of Medical Sciences, Yazd, IR Iran

4Shiraz University of Medical Sciences, Shiraz, IR Iran

International Cardiovascular Research Journal:Vol. 16, issue 1; e123932

Published online:Mar 31, 2022

Article type:Case Report

Received:Mar 07, 2022

Accepted:Apr 18, 2022

This article has been retracted. See Retraction Notice: "Congenital Left Atrial Appendage Aneurysm:A Case Report" [Int Cardio Res J. 2022;16(1):e123932].

How to Cite:Bazrafshan H, Moaref A, Salimi A, Fakhar R, Sarejloo S, et al. [Retracted Article] Congenital Left Atrial Appendage Aneurysm:A Case Report. Int Cardiovasc Res J. 2022;16(1):e123932. doi:

Abstract

Introduction: Left atrial appendage aneurysm is an infrequent abnormality presenting as atrial tachyarrhythmia, progressive dyspnea, atypical chest pain, and systemic thromboembolism. Surgical excision is considered to prevent fatal complications, even in asymptomatic cases. The present study aimed to report a 20-year-old male who presented with sudden onset palpitation and dyspnea.
Case Presentation: The case was really novel, because congenital left atrial appendage aneurysm was accompanied by dilated cardiomyopathy and Left Ventricular (LV) non-compaction. Electrocardiography (ECG) showed atrial fibrillation with Rapid Ventricular Response (RVR) secondary to a massive congenital left atrial appendage aneurysm. At first, left-sided weakness was diagnosed. In the next Computed Tomography (CT) scan performed in the hospital, right temporoparietal hypodensity was detected, which was in favor of right Middle Cerebral Artery (MCA) territory infarction that progressed with hemorrhagic transformation.
Conclusion: The patient did not accept surgical treatment and was discharged with medical therapy (oral anticoagulants and antiarrhythmic medications). He was expired as a result of multiple strokes.

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Author(s):

Hanieh Bazrafshan:[PubMed][Scholar]
Alireza Moaref:[PubMed][Scholar]
Amirhossein Salimi:[PubMed][Scholar]
Reza Fakhar:[PubMed][Scholar]
Shirin Sarejloo:[PubMed][Scholar]
Abdolali Zolghadrasli:[PubMed][Scholar]

The Official Annually Journal of Cardiovascular Research Center, Shiraz University of Medical Sciences

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[Retracted Article] Congenital Left Atrial Appendage Aneurysm:A Case Report

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