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首页> 外文期刊>Journal of Clinical and Diagnostic Research >Embryonal Rhabdomyosarcoma of Testis- A Case Report
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Embryonal Rhabdomyosarcoma of Testis- A Case Report

机译：睾丸胚性横纹肌肉瘤1例

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Embroynal Rhabdomyosarcoma of the testis is a rare and aggressive tumour, mostly seen in children and young adults. It usuallyoriginates from the para testicular tissue. Intra testicular rhabdomyosarcoma of testis is a rare entity. The authors present acase of testicular rhabdomyosarcoma in a 28-year-old male patient. The patient presented to the surgical OPD with a painlessscrotal mass of two months duration. A clinical diagnosis of testicular mass was made and patient was investigated and treatedaccordingly. Ultrasound (USG) revealed a right sided testicular mass measuring 16×6 cm. Patient underwent right sided inguinalorchidectomy. On microscopic examination tumour had varying degrees of cellularity, alternating densely packed hypercellularareas of oval to spindle shaped cells showing vesicular nucleus and pleomorphism along with loosely textured myxoid areasin between. IHC for keratin, Alpha-Fetoprotein (AFP), Inhibin and CD 117 were negative while Immunohistochemistry (IHC) formyogenin was positive. On basis of histopathology and IHC a fnal diagnosis of Embryonal Rhabdomyosarcoma was given. Intratesticular rhabdomyosarcoma of the testis is a rare tumour but should be kept in mind when dealing with a case of scrotal mass.Rarity of this entity makes it a strong learning point for our fellow clinicians and pathologists.
机译：睾丸胚性横纹肌肉瘤是一种罕见的侵袭性肿瘤，主要见于儿童和年轻人。它通常起源于睾丸旁组织。睾丸内睾丸横纹肌肉瘤是一种罕见的实体。作者介绍了一例28岁男性患者的睾丸横纹肌肉瘤。患者接受了两个月的无痛阴囊肿块手术OPD。进行了睾丸肿块的临床诊断，并对患者进行了调查和治疗。超声（USG）显示右侧睾丸肿块尺寸为16×6 cm。患者进行了右侧腹股沟睾丸切除术。在显微镜下检查，肿瘤具有不同程度的细胞性，从椭圆形到纺锤形细胞的密集堆积的高细胞区交替出现，表现出水泡状核和多态性，其间存在松散的类胶状体区域。角蛋白，α甲胎蛋白（AFP），抑制素和CD 117的IHC阴性，而肌成蛋白的免疫组织化学（IHC）阳性。根据组织病理学和IHC，最终诊断为胚胎性横纹肌肉瘤。睾丸内横纹肌肉瘤是一种罕见的肿瘤，但在处理阴囊肿块时应牢记。这个实体的稀有性使其成为我们临床医生和病理学家的重要学习点。

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