Kondo Hideaki, Horikawa Naoki, Hayashi Yoshiki, Fujimoto Kiyohide, Hirao Yoshihiko
Department of Urology, Tane General Hospital.
Hinyokika Kiyo. 2003 Jul;49(7):381-3.
A 53-year-old man came to our hospital complaining of painful induration in the left scrotum. It was difficult to determine by manual palpation whether the induration was derived from the testis or paratesticular tissues including epididymis. Computerized tomographic scanning and ultrasonography revealed a left paratesticular mass, 3 cm in diameter, with unclear margin of the atrophic testis, which was suspected as originating from the epididymis. Although tumor extirpation was intended, he underwent inguinal orchiectomy due to strong adhesion of the mass to the ipsilateral atrophic testis. The tumor was opalescent, gum elastic, and solid, measuring 5 x 3 x 2 cm in size. Histopathological examination revealed a primary leiomyoma of the epididymis. The details of this rare case of primary epididymal leiomyoma that originated from the epididymal tail are reported herein.
一名53岁男性因左侧阴囊疼痛性硬结前来我院就诊。通过手法触诊很难确定硬结是来源于睾丸还是包括附睾在内的睾丸旁组织。计算机断层扫描和超声检查显示左侧睾丸旁有一肿块,直径3厘米,萎缩睾丸的边缘不清,怀疑起源于附睾。尽管打算进行肿瘤切除,但由于肿块与同侧萎缩睾丸粘连严重,他接受了腹股沟睾丸切除术。肿瘤呈乳白色、橡皮样且质地坚实,大小为5×3×2厘米。组织病理学检查显示为附睾原发性平滑肌瘤。本文报道了这例罕见的起源于附睾尾部的原发性附睾平滑肌瘤的详细情况。