Sule J D, Lemmers M J, Barry J M
Division of Urology, Oregon Health Sciences University, Portland.
J Urol. 1993 Dec;150(6):1917-9. doi: 10.1016/s0022-5347(17)35935-9.
We report a rare case of scrotal arteriovenous malformation in an adolescent. Arteriovenous malformation of the scrotum is distinguished radiographically and histologically by numerous arterioles and thick walled veins with no intervening capillary bed. The cardinal sign is a bruit. Complete excision is recommended as definitive treatment. Preoperative angio-embolization may be helpful but it should not be relied upon for clinical resolution.
我们报告一例青少年阴囊动静脉畸形的罕见病例。阴囊动静脉畸形在影像学和组织学上的特征是有大量小动脉和厚壁静脉，其间无毛细血管床。主要体征是血管杂音。建议将完整切除作为确定性治疗方法。术前血管栓塞可能有帮助，但不应依赖其实现临床治愈。
