Extraskeletal Ewing Sarcoma Disguised as a Vascular Malformation.

IF 0.5 Q4 SURGERY
Sanjay Kumar Giri, Akanksha Rajpoot, Santanu Suba
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引用次数: 0

Abstract

Extraskeletal Ewing sarcoma (EES) is a rare entity, accounting for only 3% of lesions encountered in upper extremity. We present two paediatric patients, who were initially diagnosed with a vascular malformation based on clinical assessment and imaging. Final histopathology revealed Ewing sarcoma of soft tissue origin, confirmed by immunohistochemical analysis. Hand surgeons, who are routinely approached for a myriad of hand pathologies, should be wary and consider EES as a differential when treating such lesions. A multidisciplinary approach with an appropriate treatment algorithm can help in a speedy diagnosis, improving the long-term prognosis of the disease. Level of Evidence: Level V (Therapeutic).

伪装成血管畸形的骨外尤文肉瘤
骨外尤文肉瘤(EES)是一种罕见病,仅占上肢病变的 3%。我们介绍了两名儿童患者,根据临床评估和影像学检查,他们最初被诊断为血管畸形。经免疫组化分析证实,最终的组织病理学检查显示为软组织来源的尤文肉瘤。手外科医生在治疗此类病变时应提高警惕,并将 EES 作为鉴别诊断。采用多学科方法和适当的治疗算法有助于快速诊断,改善疾病的长期预后。证据等级:五级(治疗)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.90
自引率
0.00%
发文量
304
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