Ikoma F, Shima H
Department of Urology, Hyogo College of Medicine, Japan.
J Pediatr Surg. 1991 Jul;26(7):858-61. doi: 10.1016/0022-3468(91)90157-o.
The location anomaly of the verumontanum has not been described in the literature. We confirmed that the verumontanum was located either in the sphincteric or bulbous urethra in 61 of 477 patients with hypospadias (12.8%) through endoscopic examination and urethorgraphy. There was a patient with bilateral cryptorchidism who had distal location of the verumontanum. The patients with hypospadias and caudal migration of the verumontanum showed significantly low response of testosterone to human chorionic gonadotropin stimulation compared with normal controls. The incidence of caudal migration of the verumontanum was higher in the patients with a severe degree of hypospadias than in those with mild hypospadias. These results suggest that distal location of the verumontanum may be the result of an insufficient action of androgens during the period of critical sexual differentiation in the male embryo. We call this phenomenon caudal migration of the verumontanum, which seems to be a new clinical entity.
精阜的位置异常在文献中尚未见描述。我们通过内镜检查和尿道造影证实,在477例尿道下裂患者中有61例(12.8%)的精阜位于括约肌或球部尿道。有1例双侧隐睾患者的精阜位置靠下。与正常对照组相比,尿道下裂且精阜向尾侧移位的患者对人绒毛膜促性腺激素刺激的睾酮反应明显较低。重度尿道下裂患者精阜向尾侧移位的发生率高于轻度尿道下裂患者。这些结果表明,精阜位置靠下可能是男性胚胎关键性别分化期雄激素作用不足的结果。我们将这种现象称为精阜向尾侧移位,这似乎是一种新的临床实体。