Goubara M, Fujita T, Wada O, Okano M, Akino H, Isomatu Y, Muranaka K, Kanimoto Y, Shimizu Y, Okada K
Department of Urology, Fukui Medical School.
Hinyokika Kiyo. 1989 Oct;35(10):1801-5.
A case of rhabdomyosarcoma of the spermatic cord in a 6-year-old boy is reported. On February 26, 1986, he visited Nakamura Hospital with the chief complaint of enlargement of the left scrotal content. The contralateral scrotum was normal. The left scrotal content was a hard thumb-head-sized tumor. The left testis and epididymis were not distinguishable from the tumor. On the same day, left high inguinal orchiectomy was performed. The tumor was 3.5 by 2.5 by 2.5 cm in size and was distinguishable from the testis, epididymis and tunica vaginalis. Histopathological findings were embryonal rhabdomyosarcoma and it appeared to have originated from the spermatic cord. Two years after operation, the boy is living without metastasis. Including our experience, 101 cases of the paratesticular rhabdomyosarcoma found in Japanese literature are reviewed and briefly discussed.
报告了一例6岁男孩精索横纹肌肉瘤的病例。1986年2月26日，他因左侧阴囊内容物肿大为主诉就诊于中村医院。对侧阴囊正常。左侧阴囊内容物为一个拇指头大小的硬肿瘤。左侧睾丸和附睾与肿瘤无法区分。同一天，进行了左侧高位腹股沟睾丸切除术。肿瘤大小为3.5×2.5×2.5厘米，与睾丸、附睾和鞘膜可区分。组织病理学检查结果为胚胎性横纹肌肉瘤，似乎起源于精索。术后两年，该男孩无转移存活。结合我们的经验，对日本文献中发现的101例睾丸旁横纹肌肉瘤病例进行了回顾并简要讨论。
