Li Hao-Peng, Ye Xian-Wang, Wang Hai-Tao
Department of Radiology, Ningbo Women and Children's Hospital.
Department of Radiology, Ningbo No. 1 Hospital.
Medicine (Baltimore). 2020 Apr;99(16):e19748. doi: 10.1097/MD.0000000000019748.
Right atrial aneurysm (RAA) is a rare congenital heart disease (CHD) that usually shows no symptom and is discovered occasionally. This paper introduces the clinical and imaging data obtained in 2 RAA patients and presents a related literature review with the aim of increasing understanding of this disease.
One case showed chest distress, while the other showed symptoms on physical examination and positive signs.
Both of these 2 cases were diagnosed with RAA based on ultrasonography, computed tomography angiography (CTA), and enhanced magnetic resonance imaging (MRI) examinations.
One patient was orally administered warfarin anticoagulant therapy, while the other was given amiodarone to control arrhythmia as well as warfarin anticoagulant therapy.
The clinical symptoms of both cases were not aggravated.
RAA is a rare cardiac anomaly that can induce severe complications, and it is mainly diagnosed based on imaging examinations. Conservative treatment and regular imaging monitoring are recommended for asymptomatic patients with no high-risk factors, while surgical treatment should be performed in symptomatic patients with high-risk factors.
右心房瘤(RAA)是一种罕见的先天性心脏病(CHD),通常无症状,偶尔被发现。本文介绍了2例RAA患者的临床和影像学资料,并进行相关文献复习,旨在提高对该疾病的认识。
1例表现为胸部不适,另1例在体格检查时有症状及阳性体征。
这2例均基于超声心动图、计算机断层血管造影(CTA)和增强磁共振成像(MRI)检查诊断为RAA。
1例患者口服华法林抗凝治疗,另1例给予胺碘酮控制心律失常以及华法林抗凝治疗。
2例患者的临床症状均未加重。
RAA是一种罕见的心脏异常,可引发严重并发症,主要依靠影像学检查进行诊断。对于无高危因素的无症状患者,建议采取保守治疗并定期进行影像学监测,而对于有高危因素的有症状患者,则应进行手术治疗。