Suppr超能文献

心脏计算机断层扫描显示,一名儿童因先天性主动脉狭窄继发亚急性感染性心内膜炎,出现升主动脉霉菌性动脉瘤。

Ascending aorta mycotic aneurysm in a child secondary to subacute infective endocarditis on the basis of congenital aortic stenosis demonstrated by cardiac computerized tomography.

作者信息

Gemalmaz Hüseyin, Tok Özge Ö, Bingöl Gülsüm, Bakan Selim, Sari Ibrahim, Korkmaz Ali A

机构信息

Cardiovascular Surgery Department, Memorial Bahçelievler Hospital, Istanbul, Turkey.

Cardiology Department, Memorial Bahçelievler Hospital, Istanbul, Turkey.

出版信息

J Card Surg. 2021 Mar;36(3):1150-1153. doi: 10.1111/jocs.15344. Epub 2021 Jan 21.

Abstract

Infective endocarditis (IE) is rarely seen in children, and it can cause significant morbidity and mortality. Congenital heart disease is a predisposing cardiac condition for IE and has an increasing prevalence. A mycotic aortic aneurysm is a rare disease due to infection and it has been reported that it may be a result of IE. We present a 10-year-old boy who was referred to our cardiovascular surgery department due to severe aortic stenosis (AS). Transthoracic echocardiography revealed calcific severe AS and computerized tomography (CT) angiography was performed to better evaluate the ascending aorta. CT angiography demonstrated a saccular aneurysm of the ascending aorta. The underlying pathology was considered as chronic IE on top of congenital AS with an unknown number of cusps. Histologic findings supported our diagnosis and accompanied by a saccular aneurysm. The patient underwent a successful aortic root enlargement, mechanical aortic valve replacement, and ascending aorta repair surgery.

摘要

感染性心内膜炎(IE)在儿童中很少见,但可导致严重的发病率和死亡率。先天性心脏病是IE的易患心脏疾病,且患病率呈上升趋势。霉菌性主动脉瘤是一种由感染引起的罕见疾病,据报道它可能是IE的结果。我们报告一名10岁男孩,因严重主动脉瓣狭窄(AS)转诊至我们的心血管外科。经胸超声心动图显示钙化性严重AS,并进行了计算机断层扫描(CT)血管造影以更好地评估升主动脉。CT血管造影显示升主动脉有一个囊状动脉瘤。潜在病理被认为是先天性AS基础上的慢性IE,瓣叶数量不明。组织学检查结果支持我们的诊断,且伴有囊状动脉瘤。该患者成功接受了主动脉根部扩大、机械主动脉瓣置换和升主动脉修复手术。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验