Daskalopoulos E I, Baskin L, Duckett J W, Snyder H M
Children's Hospital of Philadelphia, Philadelphia.
Urology. 1993 Dec;42(6):708-12. doi: 10.1016/0090-4295(93)90540-q.
We treated 30 patients aged six months to nine years with congenital penile curvature from 1988 to 1993. Twenty-four patients appeared to have a primary curvature with normal corpus spongiosum. In 12 of these 24 patients dissecting skin and dartos fascia were adequate to straighten the penis. In the other 12 patients, artificial erection demonstrated a varied degree of convexity of the penis after the skin and dartos fascia release, implying a disproportion of the corpora cavernosa bodies. We corrected this deformity using dorsal tumica albuginea plications (TAP). The remaining 6 patients presented with a primary curvature and hypoplastic urethra. In 5 of these patients we divided the hypoplastic midportion of the urethra leaving the meatus naturally on the glans and replaced the midurethral segment using a tubularized island flap. Of these 5 patients 2 required TAP for penile straightening. The final patient with a hypoplastic urethra was managed by preserving the urethral plate and applying an only island flap urethroplasty. Complications were one fistula and two mild ventral penile curvatures, presently not severe enough for reoperation (mean follow-up 2.6 years). We present a systematic approach for the repair of congenital penile curvature using intraoperative artificial erection, TAP, and the island flap urethroplasty when needed.
1988年至1993年期间,我们对30例年龄在6个月至9岁的先天性阴茎弯曲患者进行了治疗。24例患者表现为原发性弯曲且海绵体正常。在这24例患者中,有12例通过解剖皮肤和肉膜筋膜足以使阴茎伸直。在另外12例患者中,人工勃起显示在皮肤和肉膜筋膜松解后阴茎有不同程度的凸度,这意味着海绵体大小不均衡。我们采用背侧白膜折叠术(TAP)纠正了这种畸形。其余6例患者表现为原发性弯曲和尿道发育不全。在这6例患者中,有5例我们将发育不全的尿道中段离断,使尿道口自然位于龟头,并使用带蒂岛状皮瓣替代中段尿道。在这5例患者中,有2例需要进行TAP以矫正阴茎弯曲。最后1例尿道发育不全的患者通过保留尿道板并仅施行岛状皮瓣尿道成形术进行治疗。并发症包括1例尿瘘和2例轻度阴茎腹侧弯曲,目前严重程度尚不足以进行再次手术(平均随访2.6年)。我们提出了一种系统性方法,在术中使用人工勃起、TAP以及必要时的岛状皮瓣尿道成形术来修复先天性阴茎弯曲。