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多叶状瓦氏窦瘤破入室间隔并破裂入左心室:一例报告

Multilobulated Sinus of Valsalva Aneurysm Dissecting into the Interventricular Septum (DAIS) and Rupturing into Left Ventricle: A Case Report.

作者信息

Ghosh Soumitra, Bootla Dinakar, Barward Parag, Sharma Arun

机构信息

Department of Cardiology, Advanced Cardiac Centre, Post Graduate Institute of Medical Education & Research, Sector 12, Chandigarh 160012, India.

Department of Radiodiagnosis, Post Graduate Institute of Medical Education & Research, Sector 12, Chandigarh 160012, India.

出版信息

Eur Heart J Case Rep. 2022 Feb 7;6(2):ytac019. doi: 10.1093/ehjcr/ytac019. eCollection 2022 Feb.

Abstract

BACKGROUND

Dissecting aneurysm of sinus of Valsalva (SOV) into the interventricular septum is a rare entity. Multilobulated form of dissection rupturing into the left ventricle (LV) has never been reported in the literature.

CASE SUMMARY

A 52-year-old male presented with dyspnoea and palpitation with wide pulse pressure and peripheral signs of distal run-off and a continuous murmur along the left parasternal area. Echocardiography revealed dilated right coronary cusp (RCC), which burrowed into the interventricular septum (IVS), forming multi-loculated cystic lesion which ruptured into LV with associated restrictive ventricular septal defect (VSD) and severe aortic regurgitation. Computed tomography (CT) angiography confirmed a 4.8 cm × 5.3 cm × 5.4 cm multiseptated aneurysm. The surgery involved excision of the aortic valve (AV) with the sinus, ligation of its penetrating portion at the crest of IVS, closure of VSD, and AV replacement. Postoperative echocardiography showed the complete collapse of the IVS component of the SOV aneurysm and the normally functioning mechanical AV.

DISCUSSION

Dissecting aneurysm into the IVS is a rare variant of SOV aneurysm, usually arising from RCC. It is mostly congenital in origin and has wide variety of presentations like congestive heart failure, palpitations, recurrent syncope, chest pain, sudden cardiac arrest, infective endocarditis, cerebral infarction, or asymptomatic. Aortic regurgitation is present in 30-50% of cases. Conduction disturbances from first-degree block to complete heart block are common. Echocardiogram, CT angio, and magnetic resonance imaging are useful for diagnosis. Surgical repair is the only option for treatment.

摘要

背景

瓦尔萨尔瓦窦(SOV)夹层动脉瘤破入室间隔是一种罕见的疾病。文献中从未报道过呈多叶状且破入左心室(LV)的夹层形式。

病例摘要

一名52岁男性因呼吸困难和心悸就诊,伴有脉压增宽、远端血流灌注的外周体征以及左胸骨旁区域连续性杂音。超声心动图显示右冠状动脉瓣叶(RCC)扩张,该瓣叶向室间隔(IVS)内延伸,形成多房性囊性病变,破入左心室,伴有相关的限制性室间隔缺损(VSD)和严重主动脉瓣反流。计算机断层扫描(CT)血管造影证实为一个4.8 cm×5.3 cm×5.4 cm的多房性动脉瘤。手术包括切除带有窦部的主动脉瓣(AV),在室间隔嵴处结扎其穿透部分,关闭室间隔缺损,并置换主动脉瓣。术后超声心动图显示SOV动脉瘤的室间隔部分完全塌陷,机械主动脉瓣功能正常。

讨论

破入室间隔的夹层动脉瘤是SOV动脉瘤的一种罕见变异型,通常起源于右冠状动脉瓣叶。其大多为先天性起源,有多种表现形式,如充血性心力衰竭、心悸、反复晕厥、胸痛、心脏骤停、感染性心内膜炎、脑梗死或无症状。30% - 50%的病例存在主动脉瓣反流。从一度房室传导阻滞到完全性心脏传导阻滞的传导障碍很常见。超声心动图、CT血管造影和磁共振成像对诊断有帮助。手术修复是唯一的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ac5/8874869/0d64bc7b08fe/ytac019f1.jpg

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