股动脉动脉瘤并发于内膜肉瘤1例。

IF 0.5 Q4 SURGERY Turkish Journal of Surgery Pub Date : 2022-09-01 DOI:10.47717/turkjsurg.2022.4381
Fatih Yanar, Gizem Öner, Sercan Yüksel, Ahmet Salduz, İbrahim Fethi Azamat, Beyza Özçınar, Bilge Bilgic, Rana Günöz Cömert, Erol Kozanoğlu, Mehmet Kurtoğlu
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引用次数: 0

摘要

内膜血管肉瘤是一种罕见的血管恶性肿瘤,由于其症状无特异性,诊断非常困难。关于内膜血管肉瘤的诊断、治疗和随访存在争议。本病例报告的目的是评估诊断为股动脉内膜血管肉瘤的患者的诊断和治疗过程。此外,与以往的研究一致,它的目的是阐明有争议的点。患者男,33岁,因股动脉动脉瘤破裂行手术,经病理诊断为内膜血管肉瘤。临床随访发现复发,并给予化疗和放疗治疗。由于治疗无效,患者接受了包括周围组织在内的积极手术。随访10个月未见复发或转移。虽然内膜血管肉瘤是罕见的,但当发现股动脉瘤时应考虑鉴别诊断。治疗中最重要的一步是积极的手术,但应考虑在治疗中加入化疗和放疗。
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Femoral artery aneurysm developed on intimal sarcoma: Case report.

Intimal angiosarcoma is a rare vascular malignancy, and diagnosis is very difficult due to nonspecific symptoms. There are controversial points regarding the diagnosis, treatment and follow-up of intimal angiosarcomas. The purpose of this case report was to evaluate the diagnosis and treatment process of a patient diagnosed with femoral artery intimal angiosarcoma. Furthermore, in line with previous studies, it was aimed to illuminate controversial points. A 33-year-old male patient, who had been operated on due to ruptured femoral artery aneurysm, was diagnosed with intimal angiosarcoma with the pathology result. Recurrence was observed during clinical follow-up, and the patient was treated with chemotherapy and radiotherapy. Since there was no response to treatment, the patient underwent aggressive surgery including the surrounding tissues. No recurrence or metastasis was observed in the patient's 10th month follow-up. Although intimal angiosarcoma is rare, it should be considered in differential diagnosis when femoral artery aneurysm is detected. The most important step in treatment is aggressive surgery, but adding chemo-radiotherapy to the treatment should be considered.

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