精索膜肉瘤:病例报告和文献综述

Roger Ziętek, Stanisław Czeszak, Zbigniew Ziętek
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引用次数: 0

摘要

摘要 精索线粒体肉瘤是一种罕见的肿瘤。它可以从任何间质细胞结构中产生。它主要发生在老年患者身上。它表现为坚硬、无痛的阴囊内肿块。我们报告了一例 30 岁男性的病例,他有 3 年的左侧阴囊无痛性肿块病史。超声检查显示为阴囊肿块。进一步检查显示手术前无远处转移。患者接受了附睾和精索的左侧根治性 1 块睾丸切除术。最终的组织病理学检查显示,患者患的是精索卵母细胞肉瘤。考虑到组织病理学检查的结果,肿瘤学委员会不建议再做手术,只建议观察等待。经过近 4 年的随访,该患者没有接受额外的治疗。原发性阴囊线粒体肉瘤是一种特殊的肿瘤,文献中仅报道过 100 例。由于其罕见性,需要更多的研究来更好地确定最佳治疗方法。本文对文献综述和治疗策略进行了讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Leiomyosarcoma of the spermatic cord: case report and literature review
Abstract Leiomyosarcoma of the spermatic cord is a rare entity. It can arise from any mesenchymal cell of its structure. It occurs mainly in elderly patients. It presents as a firm and painless intrascrotal mass. We present a case of a 30-year-old man with a 3-year history of a painless left-sided scrotal mass. Ultra-sound examination showed a scrotal mass. Further work-up revealed no distant metastasis before surgery. A left radical 1-block orchidectomy with epididymis and spermatic cord was performed. The final histopathologic examination showed a pattern of leiomyosarcoma of the spermatic cord. Considering the result of the histopathological examination, the Onco-logical Council did not recommend any additional surgery, but only watchful waiting. Almost 4 years of follow-up have passed without additional treatment. Primary scrotal leiomyosarcoma is an exceptional entity with only 100 cases reported in the literature. Due to its rarity, additional studies are needed to better define the optimal therapeutic management. A literature review and treatment strategy are discussed.
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