Baškytė Arnolda Marija, Opulskis Donatas, Kuprytė Milda, Jankauskas Antanas, Velička Linas
Department of Vascular Surgery, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Faculty of Medicine, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Vasc Endovascular Surg. 2025 Jun 21;59(7):15385744251355185. doi: 10.1177/15385744251355185.
Primary aortic malignancy is a very rare pathology, with only 190 cases of aortic tumors reported in the literature to date. Usually, symptoms are insidious and nonspecific, so the disease is diagnosed at an advanced stage. Here, we present a case report of a primary malignant tumor of the aorta. In our case, the diagnosis was established using computed tomography angiography (CTA) and biopsy of indeterminate masses obtained during aortography. The patient underwent surgical resection of the affected aortic segment along with a tumor. Histopathological examination revealed the diagnosis of a primary malignant tumor of the aorta - angiosarcoma. Postoperatively, patient received adjuvant chemotherapy according to the standard treatment regimen for sarcoma. One month later, postoperative CT of a chest, abdomen and pelvis was performed, revealing no evidence of metastases or pathological lymph nodes in the examined areas. : Combined surgical and systemic therapies may improve overall survival.
原发性主动脉恶性肿瘤是一种非常罕见的病理情况,迄今为止文献中仅报道了190例主动脉肿瘤病例。通常,症状隐匿且不具有特异性,因此该疾病在晚期才被诊断出来。在此,我们报告一例原发性主动脉恶性肿瘤的病例。在我们的病例中,通过计算机断层血管造影(CTA)以及主动脉造影期间获取的不确定肿块活检确定了诊断。患者接受了受累主动脉段连同肿瘤的手术切除。组织病理学检查显示诊断为原发性主动脉恶性肿瘤——血管肉瘤。术后,患者根据肉瘤的标准治疗方案接受了辅助化疗。一个月后,进行了胸部、腹部和骨盆的术后CT检查,结果显示在检查区域没有转移或病理性淋巴结的迹象。联合手术和全身治疗可能会提高总体生存率。