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病例报告与文献综述:心脏血性囊肿

Case report and literature review: cardiac hematic cyst.

作者信息

Baltodano-Arellano Roberto, Alvarez-Tiburcio Eduardo, Barriales-Revilla Lucia, Bellido-Yarlequé David, Cachicatari Angela, Cupe-Chacalcaje Kelly, La Torre-Zuñiga Alan, Velarde-Acosta Kevin

机构信息

Cardiac Imaging Area of Cardiology Service, Hospital Guillermo Almenara Irigoyen - EsSalud, Lima, Peru.

School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Peru.

出版信息

Front Cardiovasc Med. 2024 Jul 30;11:1417074. doi: 10.3389/fcvm.2024.1417074. eCollection 2024.

Abstract

A 49-year-old female patient, asymptomatic, presented to the cardiology office for a right atrial mass, identified incidentally in a non-electrocardiogram (ECG)-gated contrast-enhanced computed tomography, performed for follow-up of pulmonary tuberculosis. Echocardiography, surprisingly, showed an anechogenic ovoid mass in the right atrium measuring 40 × 40 mm, implanted in the interatrial septum without affecting the tricuspid valve. ECG-gated computed tomography angiography (CTA), confirmed the dimensions of the mass, which presented homogeneous content, calcified areas, and a 12-mm pedicle implanted near the ostium of the coronary sinus. Additionally, contrast uptake and infiltration of adjacent structures were ruled out. In the surgical field, an encapsulated mass with blood content was found, which pathology reported as a hematic endocardial cyst (HEC). These are rare cardiac masses, constituting 1.5% of all primary cardiac tumors. It is usually an incidental finding, and its clinical presentation will depend on its dimensions and the intracardiac hemodynamic impact. A highlighting feature is its anechogenic content on ultrasound, however, multimodality imaging allows for making diagnostic assumptions, discerning between primary cardiac tumors, and provides morphological and hemodynamic information useful for therapeutic decision making. The age of the patient, the large size of the HEC, and its location in the interatrial septum make up a completely atypical presentation of this rare disease, which motivated this report.

摘要

一名49岁无症状女性患者因右心房肿块前往心脏病科就诊,该肿块是在为肺结核随访而进行的非心电图门控对比增强计算机断层扫描中偶然发现的。令人惊讶的是,超声心动图显示右心房有一个40×40毫米的无回声椭圆形肿块,附着在房间隔上,未影响三尖瓣。心电图门控计算机断层血管造影(CTA)证实了肿块的大小,其内容均匀,有钙化区域,在冠状窦口附近有一个12毫米的蒂。此外,排除了对比剂摄取和邻近结构浸润。在手术视野中发现了一个有血液成分的包膜肿块,病理报告为血性心内膜囊肿(HEC)。这些是罕见的心脏肿块,占所有原发性心脏肿瘤的1.5%。它通常是偶然发现的,其临床表现取决于其大小和对心内血流动力学的影响。一个突出特征是其在超声上的无回声内容,然而,多模态成像有助于做出诊断假设,区分原发性心脏肿瘤,并提供有助于治疗决策的形态学和血流动力学信息。患者的年龄、HEC的大尺寸及其在房间隔中的位置构成了这种罕见疾病的完全非典型表现,这促使了本报告的撰写。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bc6/11319172/a11b0c6b174e/fcvm-11-1417074-g001.jpg

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