Stöber U
Urologe A. 1976 Sep;15(5):227-32.
Congenital bulbar urethral stenosis arises from incomplete opening of the urogenital membrane. The etiology may possibly be genetic or else a disturbance in the maternal hormones during the embryonic phase. The diagnosis from other types of stenosis is made by urethroscopy. The urodynamic consequences are a compensatory hypertrophy of bladder muscle, in extreme cases finally followed by hydronephrosis. Symptoms of stenosis include dysuria, polyuria, enuresis, and recurrent urinary tract infection. The whole urinary tract should be investigated. At present, the operation of choice for dealing with this type of stenosis, is internal urethrotomy under direct vision (Sachse's operation). Short-term indwelling catheterization, prophylaxis against infection, and hydraulic auto-bougination (raising the internal urethral pressure by compressing the penis during micturition) help to ensure success. The percentage of complications is low. The risk of recurrence is less than with the use of electrocautery.
先天性球部尿道狭窄源于泌尿生殖膜开口不完全。其病因可能是遗传因素,也可能是胚胎期母体激素紊乱。通过尿道镜检查可与其他类型的狭窄相鉴别。其尿动力学后果是膀胱肌肉代偿性肥大,在极端情况下最终会导致肾积水。狭窄的症状包括排尿困难、多尿、遗尿和反复尿路感染。应检查整个尿路。目前,处理这类狭窄的首选手术是直视下内尿道切开术(萨克塞手术)。短期留置导尿、预防感染以及水囊扩张术(排尿时压迫阴茎以提高尿道内压)有助于确保手术成功。并发症发生率较低。与使用电灼术相比,复发风险较小。