Bahrami Mahshid, Sahba Sareh
Department of Radiology, Isfahan University of Medical Sciences, Isfahan, Iran.
Radiol Case Rep. 2024 Jul 27;19(10):4354-4357. doi: 10.1016/j.radcr.2024.06.094. eCollection 2024 Oct.
Ewing sarcoma (ES) is a rare group of undifferentiated tumors that originate from neuroectoderm. Although the overall prognosis is poor, early diagnosis and treatment by a multidisciplinary team with multimodal therapy can improve outcomes. Therefore, we present a 22-year-old female patient with primary renal ES with tumor thrombosis up to the vena cava who had radical nephrectomy and IVC tumor thrombectomy followed by adjuvant chemotherapy because a preoperative percutaneous biopsy was confirmed the diagnosis.
尤因肉瘤(ES)是一组罕见的起源于神经外胚层的未分化肿瘤。尽管总体预后较差,但由多学科团队采用多模式疗法进行早期诊断和治疗可改善治疗效果。因此,我们报告了一名22岁的女性原发性肾ES患者,其肿瘤血栓形成直至腔静脉,该患者接受了根治性肾切除术和下腔静脉肿瘤血栓切除术,随后进行辅助化疗,因为术前经皮活检确诊了该疾病。