Paratesticular epithelioid sarcoma: A rare case

Aashita, Rajiv Sharma, Vikas K Yadav, T. Divya, N. Kaur
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引用次数: 0

Abstract

Primary soft-tissue sarcomas of the paratesticular region are uncommon tumors comprising 1% of all adult sarcomas. Paratesticular epithelioid sarcoma (ES) is a rare subtype. Here, we report the case of a 68-years-old male with scrotal swelling who underwent high inguinal exploration and right orchidectomy. Histopathology and immunohistochemistry revealed paratesticular ES. Very few cases of paratesticular ES have been reported so far in the literature. Clinical presentation, investigations, treatment interventions, and prognosis have been discussed. As it can be confused with other benign and malignant conditions, diagnosis is often made on histopathological evaluation.
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睾丸旁上皮样肉瘤:罕见病例
原发于睾丸旁区域的软组织肉瘤是罕见的肿瘤,占所有成人肉瘤的1%。睾丸旁上皮样肉瘤(ES)是一种罕见的亚型。在此,我们报告一个68岁男性阴囊肿胀的病例,他接受了高腹股沟探查和右侧睾丸切除术。组织病理学和免疫组织化学显示睾丸旁ES。迄今为止,文献中报道的特发性ES病例很少。讨论了临床表现、调查、治疗干预和预后。由于它可能与其他良性和恶性疾病混淆,诊断通常是在组织病理学评估。
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自引率
0.00%
发文量
27
审稿时长
11 weeks
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