Anthonissen N, Menting T, Verkroost M, Morshuis W
Department of Cardiothoracic Surgery, Radboud University Medical Center Nijmegen, Nijmegen, The Netherlands.
Department of Vascular Surgery, Radboud University Medical Center Nijmegen, Nijmegen, The Netherlands.
EJVES Short Rep. 2016 May 10;32:4-6. doi: 10.1016/j.ejvssr.2016.04.002. eCollection 2016.
Primary angiosarcomas of the aorta are rare and because of their non-specific presentation, the initial diagnosis is often very difficult.
A 66 year old woman, initially suffering from night sweats and general malaise, is presented. A computerized tomography (CT) scan was performed which showed a filling defect of the descending aorta. This defect later caused embolic occlusion of the celiac vessels. The patient underwent surgical resection of the filling defect of the descending aorta and an embolectomy of the celiac vessels. The defect was histopathologically diagnosed as an angiosarcoma. The clinical presentation, diagnostic pitfalls, histopathological diagnosis, and the therapeutic management are discussed.
In this case report, the importance of carefully diagnosing an angiosarcoma is highlighted as the consequences could be rapid metastasization or embolization.
主动脉原发性血管肉瘤罕见,因其临床表现不具特异性,故初始诊断往往极为困难。
本文介绍了一名66岁女性,最初出现盗汗和全身不适症状。进行了计算机断层扫描(CT),显示降主动脉存在充盈缺损。该缺损后来导致腹腔血管发生栓塞性闭塞。患者接受了降主动脉充盈缺损的手术切除及腹腔血管取栓术。该缺损经组织病理学诊断为血管肉瘤。文中讨论了临床表现、诊断陷阱、组织病理学诊断及治疗处理。
在本病例报告中,强调了仔细诊断血管肉瘤的重要性,因为其后果可能是快速转移或栓塞。