胸主动脉腹主动脉血管肉瘤伴系统性高血压、贫血和内脏缺血。
Angiosarcoma of the thoracoabdominal aorta presenting with systemic hypertension, anemia, and visceral ischemia.
作者信息
Karamlou Tara, Li Melissa K, Williamson W Kent, Heller Lloyd, Wiest John W
机构信息
Department of Surgery, Oregon Health & Science University, Portland, OR, USA.
出版信息
Ann Vasc Surg. 2008 May-Jun;22(3):459-64. doi: 10.1016/j.avsg.2007.09.010. Epub 2008 Mar 25.
Aortic angiosarcomas, one of the three major types of primary aortic tumors, are exceedingly rare, with only 25 cases reported in the literature. Peripheral thromboembolic complications are the most frequently described presenting feature, and therefore, these tumors can be mistaken for aortoiliac occlusive disease. We describe a rare case of an extensive thoracoabdominal angiosarcoma that manifested with hypertension, profound anemia, and visceral ischemia in a young woman.
主动脉血管肉瘤是原发性主动脉肿瘤的三种主要类型之一，极为罕见，文献中仅报道过25例。外周血栓栓塞并发症是最常描述的临床表现，因此，这些肿瘤可能会被误诊为主髂动脉闭塞性疾病。我们描述了一例罕见的广泛胸腹主动脉血管肉瘤病例，该病例发生在一名年轻女性身上，表现为高血压、严重贫血和内脏缺血。
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