Do Thanh Hoa, Le Xuan Duong, Vu Thu Thuy, Ngo Tuan Anh, Thi Minh Hanh Ngo, Tran Quang Thai, Dinh Hoang Diep, Nguyen Huu Giap, Lam Khanh
Department of Emergency, Hanoi, Vietnam.
Department of Diagnostic Imaging, Hanoi, Vietnam.
Radiol Case Rep. 2022 Jul 14;17(9):3349-3354. doi: 10.1016/j.radcr.2022.06.048. eCollection 2022 Sep.
Primary cardiac angiosarcoma is an extremely rare, high-grade malignancy. Here, we describe the case of a 44-year-old male patient with a heart tumor in the left atrium wall, which caused a large amount of pericardial effusion that invaded the surrounding area and is visible on transthoracic echocardiography, computed tomography, and magnetic resonance imaging. The postoperative histopathological results confirmed this case as a primary cardiac epithelioid angiosarcoma.
原发性心脏血管肉瘤是一种极其罕见的高级别恶性肿瘤。在此,我们描述了一名44岁男性患者的病例,其左心房壁有一个心脏肿瘤,该肿瘤导致大量心包积液,侵犯周围区域,经胸超声心动图、计算机断层扫描和磁共振成像均可见。术后组织病理学结果证实该病例为原发性心脏上皮样血管肉瘤。