首页> 外文期刊>Journal of Cardiothoracic Surgery >Intimal aortic sarcoma mimicking ruptured thoracoabdominal type IV aneurysm. a rare case report and review of the literature
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Intimal aortic sarcoma mimicking ruptured thoracoabdominal type IV aneurysm. a rare case report and review of the literature

机译:模拟内膜主动脉肉瘤破裂的胸腹IV型动脉瘤。罕见的病例报告和文献复习

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Primary intimal aortic sarcoma represents a very rare and highly lethal medical entity. Diagnosis is made either by embolic events caused by the tumor or by surrounding tissue symptoms such as pain. Herein we report an extremely rare case of a 51-year-old man previously operated for ascending aortic aneurysm, who presented with clinical and radiological findings suggestive of a ruptured thoracoabdominal type IV aneurysm. The patient underwent radical resection of the aorta and surrounding tissue with placement of a composite 4-branched graft. The diagnosis was made by frozen section and regular histopathologic examination of the specimen and the patient received adjuvant chemotherapy. Nine months after surgery the patient is still alive and has no signs of recurrence. We review the literature and discuss the option of postoperative chemotherapy.
机译:原发性内膜主动脉肉瘤代表一种非常罕见且高度致死性的医学实体。通过肿瘤引起的栓塞事件或周围组织的症状(例如疼痛)进行诊断。在此,我们报道了一个非常罕见的病例,该病例先前曾因升主动脉瘤而手术,现年51岁,其临床和影像学表现提示胸腹IV型动脉瘤破裂。该患者接受了主动脉和周围组织的根治性切除,并植入了四分支复合移植物。诊断是通过冰冻切片和定期组织病理学检查标本进行的,患者接受了辅助化疗。手术后九个月,患者仍然活着并且没有复发的迹象。我们回顾了文献并讨论了术后化疗的选择。

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