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Primary angiosarcoma of the abdominal aorta: a case report and literature review (aortic angiosarcoma)

机译:腹主动脉原发性血管肉瘤:一例报道并文献复习(主动脉血管肉瘤)

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摘要

Fewer than 140 cases of aortic sarcoma have been reported with only 34 classified as angiosarcoma. These rare malignancies most often mimic aortoiliac occlusive or aneurysmal arteriosclerotic disease both clinically and on imaging studies, and the large majority are unexpected and diagnosed pathologically on a surgical specimen or at autopsy [1–5]. A 42-year-old woman who presented with low back pain and claudication was shown by CT and angiography to have infrarenal aortic occlusion. Angiosarcoma was an unexpected pathologic diagnosis based on tissue removed during aortobifemoral bypass surgery. Pre and postoperative CT and angiography are presented along with a review of the literature.
机译:据报道,少于140例主动脉肉瘤,其中34例归为血管肉瘤。这些罕见的恶性肿瘤最常在临床和影像学研究中模仿主动脉闭塞性或动脉瘤性动脉硬化性疾病,并且绝大多数是意外的,并且在手术标本或尸体解剖上经病理学诊断[1-5]。 CT和血管造影显示一名42岁的下腰痛和c行的女性患有肾下主动脉阻塞。血管肉瘤是一种预料不到的病理学诊断,其基于在主动脉分娩旁路手术中切除的组织。介绍了术前和术后的CT和血管造影以及文献回顾。

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