Department of Plastic Surgery, St James's Hospital, Dublin 8, Ireland.
J Plast Reconstr Aesthet Surg. 2012 Jul;65(7):977-80. doi: 10.1016/j.bjps.2011.11.062. Epub 2012 Jan 11.
Epithelioid sarcoma, first described by Enzinger in 1970, classically presents in young adults and usually arises in the distal extremities. The proximal-type variant, first described in 1997 as a rare aggressive form of sarcoma, usually arises more proximally. It carries a higher mortality rate than classical limb epithelioid sarcoma and is often resistant to multimodal treatment. We report the case of a 27-year old male who had a delayed diagnosis of proximal-type epithelioid sarcoma of the forearm. This was originally thought to be a necrotising soft tissue infection and was unfortunately metastatic at the time of eventual diagnosis. The clinical and histopathological features of this challenging tumour are discussed and the relevant literature is reviewed.
上皮样肉瘤,于 1970 年由 Enzinger 首次描述,好发于年轻成人,通常发生于四肢远端。1997 年首次描述了近端型变异型,为一种罕见的侵袭性肉瘤,通常发生于更靠近近端的部位。与经典的肢体上皮样肉瘤相比,其死亡率更高,且通常对多模式治疗有抗性。我们报告了一例 27 岁男性前臂近端型上皮样肉瘤的延迟诊断病例。最初被误诊为坏死性软组织感染,最终诊断时已发生转移,令人遗憾。我们讨论了这一具有挑战性的肿瘤的临床和组织病理学特征,并复习了相关文献。