Large dissecting sinus of Valsalva aneurysm creating a 'triple ventricle' appearance: case report.

IF 0.8 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
European Heart Journal: Case Reports Pub Date : 2025-07-15 eCollection Date: 2025-07-01 DOI:10.1093/ehjcr/ytaf308
Swasthi S Kumar, Sudipta Mondal, Jayakrishnan Radhakrishnan, Ramya Das
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引用次数: 0

Abstract

Background: Dissecting aneurysm of the interventricular septum (DAIS) is a rare congenital or acquired anomaly which can have a progressive course. We report a large DAIS incidentally detected by a routine echocardiogram.

Case summary: An asymptomatic tricenarian was incidentally detected to a DAIS during a routine pre-operative evaluation. Multimodality imaging with cardiac CT, MRI, and aortic root angiograms confirmed the diagnosis. Work-up for infectious causes like syphilis and inflammatory causes like connective tissue disorders were negative. Patient is planned for surgical repair.

Discussion: Dissecting aneurysm of the interventricular septum is a rare anomaly with a poor prognosis. The rupture of sinus of Valsalva aneurysm is the most common cause. Infections like syphilis and infective endocarditis, connective tissue disorders (Marfan syndrome and Ehler-Danlos syndrome), autoimmune diseases (Behcet's disease, ankylosing spondylitis, systemic lupus erythematosus, Takayasu's arteritis), bicuspid aortic valve with aortopathy, atherosclerosis, surgery, or trauma are the reported causes. Such dissecting aneurysms can have a progressive course, leading to right or left ventricular outflow tract obstructions, severe aortic regurgitation, and rupture into ventricular chambers, portending a grave prognosis. Hence, surgical correction is the norm.

Valsalva动脉瘤的大解剖窦形成“三心室”外观:1例报告。
背景:室间隔夹层动脉瘤(DAIS)是一种罕见的先天性或后天性异常,其病程可呈进行性发展。我们报告一个大DAIS偶然发现常规超声心动图。病例总结:一名无症状的三岁老人在常规术前评估中偶然发现DAIS。心脏CT、MRI和主动脉根血管造影证实了诊断。梅毒等传染性疾病和结缔组织紊乱等炎症性疾病的检查结果为阴性。病人计划进行手术修复。讨论:室间隔夹层动脉瘤是一种罕见的异常,预后较差。动脉瘤窦破裂是最常见的原因。感染,如梅毒和感染性心内膜炎,结缔组织疾病(马凡氏综合征和埃勒-丹洛斯综合征),自身免疫性疾病(白塞氏病,强直性脊柱炎,系统性红斑狼疮,高雅氏动脉炎),主动脉病变,动脉粥样硬化,手术或创伤是报告的原因。这类夹层动脉瘤可呈进行性发展,可导致右或左心室流出道阻塞,严重的主动脉反流,破裂进入心室,预后严重。因此,手术矫正是常态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Heart Journal: Case Reports
European Heart Journal: Case Reports Medicine-Cardiology and Cardiovascular Medicine
CiteScore
1.30
自引率
10.00%
发文量
451
审稿时长
14 weeks
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