Xiang Yingming, Yan Liping, Lin Xia, Zhang Xiangyan, Zhang Fangbiao, Wu Zhijun
Lishui Municipal Central Hospital, Lishui, China.
Front Surg. 2021 May 28;8:666389. doi: 10.3389/fsurg.2021.666389. eCollection 2021.
Epithelioid angiosarcoma arising in schwannoma is an extremely rare mesenchymal tumor that accounts for only 1 to 2% of all sarcomas. This type of tumor occurs in all parts of the body, most often in the skin and soft tissues and rarely in the mediastinum. The present study describes the case of an asymptomatic, 58-year-old male who presented with epithelioid angiosarcoma in the posterior mediastinum during a physical examination. Enhanced computed tomography of the chest revealed a 3.5 × 3.1-cm mass in the posterior mediastinum. Thoracoscopic mediastinal mass resection was performed under general anesthesia due to the possibility that the tumor was malignant. Pathological examination revealed the presence of angiosarcoma and schwannoma components. Immunohistochemical staining for cluster of differentiation (CD) 31, CD34, early growth response (EGR), vimentin, Sry-related HMG box (SOX)-10 and S-100 was strongly positive. The patient recovered and was discharged on postoperative day 5. Two months postsurgery, the patient returned for evaluation, and no evidence of tumor recurrence was observed.
起源于神经鞘瘤的上皮样血管肉瘤是一种极其罕见的间叶组织肿瘤,仅占所有肉瘤的1%至2%。这种类型的肿瘤可发生于身体的各个部位,最常见于皮肤和软组织,很少发生于纵隔。本研究描述了一例无症状的58岁男性病例,该患者在体检时发现后纵隔存在上皮样血管肉瘤。胸部增强计算机断层扫描显示后纵隔有一个3.5×3.1厘米的肿块。由于肿瘤可能为恶性,因此在全身麻醉下进行了胸腔镜纵隔肿块切除术。病理检查显示存在血管肉瘤和神经鞘瘤成分。分化簇(CD)31、CD34、早期生长反应(EGR)、波形蛋白、性别决定区Y相关高迁移率族盒(SOX)-10和S-100的免疫组织化学染色呈强阳性。患者康复并于术后第5天出院。术后两个月,患者返回进行评估,未观察到肿瘤复发的迹象。