主动脉血管肉瘤:血管肿瘤中一种罕见的侵袭性血管恶性肿瘤1例报告。

IF 0.7
Arnolda Marija Baškytė, Donatas Opulskis, Milda Kuprytė, Antanas Jankauskas, Linas Velička
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引用次数: 0

摘要

摘要:原发性主动脉恶性肿瘤是一种非常罕见的病理,迄今为止文献中仅报道了190例主动脉肿瘤。通常,症状是隐匿的和非特异性的,所以这种疾病在晚期才被诊断出来。目的:在此,我们报告一例原发性主动脉恶性肿瘤。在我们的病例中,诊断是通过计算机断层血管造影(CTA)和在主动脉造影中获得的不确定肿块的活检来建立的。方法:患者手术切除病变主动脉段并合并肿瘤。组织病理检查显示为原发性主动脉恶性肿瘤-血管肉瘤。术后患者按肉瘤标准治疗方案接受辅助化疗。结果:术后1个月行胸腹骨盆CT检查,未见病灶转移及病理淋巴结。结论:手术联合全身治疗可提高总生存率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unveiling Aortic Angiosarcoma: A Rare and Aggressive Vascular Malignancy in Vascular Oncology - A Case Report.

Introduction: 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. Objective: 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. Methods: 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. Results: 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. Conclusion: Combined surgical and systemic therapies may improve overall survival.

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