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Imaging features of soft tissue epithelioid angiosarcoma in the lower extremity: A case report

机译:下肢软组织上皮样血管肉瘤的影像学特征:一例报告

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摘要

Epithelioid angiosarcomas are extremely rare malignant tumors formed from endothelial cells. The majority of studies reporting these tumors have been concerned with the clinical and pathological aspects, with limited reporting of radiological diagnosis. The aim of the present study was to provide a reference to improve understanding of diagnosis, treatment choice and prognosis assessment of epithelioid angiosarcoma. The current study reports the case of a 44-year-old woman with epithelioid angiosarcoma located in the deep soft tissue of the lower extremities. Physical examination of the right thigh revealed a palpable hard mass and movement was clearly restricted and painful. X-ray, computed tomography (CT) scans and magnetic resonance imaging (MRI) were used to evaluate the imaging features of the tumor. Using X-ray and CT scanning, an inhomogenous tumor with osteolytic osseous destruction was observed. MRI revealed that the bordering skeletal muscles were infiltrated. The patient was treated with palliative surgery and chemotherapy, but succumbed to disease 1 year later.
机译:上皮样血管肉瘤是由内皮细胞形成的极为罕见的恶性肿瘤。报告这些肿瘤的大多数研究都与临床和病理方面有关,对放射学诊断的报道有限。本研究的目的是为提高对上皮样血管肉瘤的诊断,治疗选择和预后评估的了解提供参考。当前的研究报道了一名44岁的女性,其上皮样血管肉瘤位于下肢深部软组织中。右大腿的身体检查显示明显的硬块,运动明显受限且疼痛。 X射线,计算机断层扫描(CT)扫描和磁共振成像(MRI)用于评估肿瘤的成像特征。使用X射线和CT扫描,观察到具有溶骨性破坏的不均匀肿瘤。 MRI显示,周围的骨骼肌已浸润。该患者接受姑息手术和化学疗法治疗,但在一年后死于疾病。

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