Rare Case of Cavernous Haemangioma of the Right Atrium with Probable Hepatic Haemangioma

IF 0.6 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
S. Harrison
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引用次数: 0

Abstract

Cardiac haemangiomas are rare causes of atrial masses. This case report is of a 44-year-old male who presented with a right atrial mass that was found incidentally on a CT performed for renal colic. The mass was further investigated with a transthoracic echocardiogram that showed that it was echodense and arising from the Eustachian valve in the right atrium. Coronary angiogram revealed large well-developed atrial branches that crossed superiorly over the left atrium and entered the mass in the right atrium. Surgical resection was undertaken, and this confirmed that the mass had a fleshy, encapsulated appearance with a sessile stalk. Histology demonstrated a cavernous haemangioma. The patient had a residual small defect in the interatrial septum postoperatively but otherwise made a good recovery.
右心房海绵状血管瘤合并肝血管瘤的罕见病例
心脏血管瘤是引起心房肿块的罕见原因。本病例报告是一位44岁男性患者,他在肾绞痛的CT检查中偶然发现了右心房肿块。经胸超声心动图显示肿块回声密集,起源于右心房的咽鼓瓣。冠状动脉造影显示发育良好的大心房分支在左心房上方穿过并进入右心房肿块。手术切除,这证实了肿块有肉质,包被外观与无柄柄。组织学表现为海绵状血管瘤。患者术后房间隔有残留的小缺损,但其他方面恢复良好。
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来源期刊
Case Reports in Cardiology
Case Reports in Cardiology CARDIAC & CARDIOVASCULAR SYSTEMS-
自引率
0.00%
发文量
63
审稿时长
13 weeks
期刊介绍: Case Reports in Cardiology is a peer-reviewed, Open Access journal that publishes case reports and case series related to hypertension, arrhythmia, congestive heart failure, valvular heart disease, vascular disease, congenital heart disease and cardiomyopathy.
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