膀胱发育不全与不完全性肾重复畸形：以可控性回肠膀胱术作为确定性治疗方法。
Bladder agenesis and incomplete kidney duplication: Ileal reservoir with continent diversion as definitive treatment.
作者信息
Pacheco-Mendoza Byron Alexis, González-Ledón Fernando J, Díaz-Pardo Mario, Soto-Blanquel Juan L, Castelán-Martínez Osvaldo Daniel
机构信息
Urology Department, Hospital Infantil de México Federico Gómez, Mexico City, Mexico;
Clinical Epidemiology Unit, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.
出版信息
Can Urol Assoc J. 2015 Mar-Apr;9(3-4):E142-4. doi: 10.5489/cuaj.2534.
Bladder agenesis is an extremely rare entity. A 12-year-old female patient presented with urinary incontinence, recurrent urinary tract infections, visible vaginal introitus and urethra, and two holes at the vulvar vestibule. An investigation revealed bladder agenesis. Surgery confirmed the absence of bladder, and ileal reservoir in omega (Ω) was performed with continent diversion. At the 30-month follow-up, there was no complication in clean intermittent catheterization.
膀胱发育不全是一种极其罕见的病症。一名12岁女性患者出现尿失禁、反复尿路感染、可见阴道开口和尿道，以及外阴前庭有两个孔。一项检查显示为膀胱发育不全。手术证实膀胱缺失，并进行了Ω形回肠储尿囊及可控性尿流改道术。在30个月的随访中，清洁间歇性导尿未出现并发症。
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