Multimodality Imaging Uncovers Giant Coronary Artery Aneurysm Mimicking Cardiac Tumor.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL American Journal of Case Reports Pub Date : 2024-11-17 DOI:10.12659/AJCR.945434
Karoline Bjerg Dam-Huus, Hans Gustav Hørsted Thyregod, Redi Pecini, Morten Holdgaard Smerup, Ekim Seven, Ida Arentz Taraldsen, Jesper James Linde
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Abstract

BACKGROUND Giant coronary artery aneurysms (CAA) are extremely rare and can mimic cardiac tumors. Therefore, an unidentified mass in the heart requires a multimodality imaging approach for accurate diagnosis and guidance of further management, which for CAAs often include surgical intervention to prevent complications such as thrombosis or rupture. CASE REPORT A 37-year-old man presented with non-specific symptoms. A CT scan revealed multiple bilateral pulmonary embolisms and an indeterminate mass in the right atrium. Transthoracic echocardiography (TTE) showed a suspected cardiac tumor, and further imaging with transesophageal echocardiography (TEE), magnetic resonance imaging (MRI), and position emission tomography (PET) indicated a local inhomogeneous mass with arterial perfusion. A preoperative cardiac CT found the mass to be a giant thrombosed CAA in the proximal right coronary artery compressing the tricuspid annulus. The patient underwent successful surgical excision of the CAA along with coronary artery bypass grafting. Postoperative management included lifelong administration of acetylsalicylic acid and a 3-month course of anticoagulant therapy. Histopathology excluded systemic vasculitis, indicating a congenital etiology for the CAA. CONCLUSIONS This case illustrates the indispensable role of coronary CT angiography in accurately diagnosing and managing complex cardiac conditions. Due to the complex and diverse nature of suspected cardiac tumors, cardiac CT should always be added in the diagnostic workup to describe the coronary anatomy in relation to the tumor and to identify a differential diagnosis such as a giant coronary aneurysm.

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多模态成像发现模仿心脏肿瘤的巨大冠状动脉动脉瘤
背景 巨大冠状动脉瘤(CAA)极为罕见,可与心脏肿瘤相似。因此,如果心脏中出现不明肿块,需要采用多模态成像方法进行准确诊断,并指导进一步的治疗,对于 CAA,通常包括手术干预,以防止血栓形成或破裂等并发症。病例报告 一名 37 岁的男子出现非特异性症状。CT 扫描显示双侧多发肺栓塞,右心房有一不确定肿块。经胸超声心动图(TTE)显示疑似心脏肿瘤,进一步的经食道超声心动图(TEE)、磁共振成像(MRI)和体位发射断层扫描(PET)显示有动脉灌注的局部不均匀肿块。术前心脏 CT 发现肿块是右冠状动脉近端巨大的血栓性 CAA,压迫三尖瓣环。患者接受了冠状动脉旁路移植手术,成功切除了CAA。术后管理包括终身服用乙酰水杨酸和为期 3 个月的抗凝治疗。组织病理学检查排除了系统性血管炎的可能性,表明 CAA 的病因是先天性的。结论 本病例说明了冠状动脉 CT 血管造影术在准确诊断和处理复杂心脏疾病中不可或缺的作用。由于疑似心脏肿瘤的复杂性和多样性,在诊断工作中应始终加入心脏 CT,以描述与肿瘤相关的冠状动脉解剖结构,并鉴别巨大冠状动脉瘤等鉴别诊断。
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来源期刊
American Journal of Case Reports
American Journal of Case Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
599
期刊介绍: American Journal of Case Reports is an international, peer-reviewed scientific journal that publishes single and series case reports in all medical fields. American Journal of Case Reports is issued on a continuous basis as a primary electronic journal. Print copies of a single article or a set of articles can be ordered on demand.
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