Wehner M S, Humphreys J L, Sharkey F E
Department of Pathology, University of Texas Health Science Center at San Antonio, San Antonio, TX 78284-7750, USA.
Arch Pathol Lab Med. 2000 Oct;124(10):1518-9. doi: 10.5858/2000-124-1518-ER.
Genital rhabdomyoma is a rare tumor of skeletal muscle origin that is usually found in the vulvar area of young women. The English literature contains only 2 previous case reports involving men, both of whom were 19 years old. One of these lesions originated in the tunica vaginalis of the testis, and the other originated in the prostate gland. We present the clinical, histologic, and immunohistochemical findings of an epididymal rhabdomyoma in a 20-year-old man. To our knowledge, this is the first such case reported in this location.
生殖器横纹肌瘤是一种罕见的起源于骨骼肌的肿瘤，通常见于年轻女性的外阴区域。英文文献中仅有2例先前报道的累及男性的病例，患者均为19岁。其中1例病变起源于睾丸鞘膜，另1例起源于前列腺。我们报告了1例20岁男性附睾横纹肌瘤的临床、组织学和免疫组化检查结果。据我们所知，这是该部位报道的首例此类病例。
