Bladder agenesis and incomplete kidney duplication: Ileal reservoir with continent diversion as definitive treatment

Authors

  • Byron Alexis Pacheco-Mendoza Urology Department,Hospital Infantil de México Federico Gómez
  • Fernando J González-Ledón Urology Department,Hospital Infantil de México Federico Gómez
  • Mario Díaz-Pardo Urology Department,Hospital Infantil de México Federico Gómez
  • Juan L Soto-Blanquel Urology Department,Hospital Infantil de México Federico Gómez
  • Osvaldo Daniel Castelán-Martínez Clinical Epidemiology Unit, Hospital Infantil de México Federico Gómez

DOI:

https://doi.org/10.5489/cuaj.2534

Keywords:

Bladder agenesis, Ileal reservoir, Continent diversion, Incomplete kidney duplication.

Abstract

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.

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Author Biography

Osvaldo Daniel Castelán-Martínez, Clinical Epidemiology Unit, Hospital Infantil de México Federico Gómez

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Published

2015-03-11

How to Cite

Pacheco-Mendoza, B. A., González-Ledón, F. J., Díaz-Pardo, M., Soto-Blanquel, J. L., & Castelán-Martínez, O. D. (2015). Bladder agenesis and incomplete kidney duplication: Ileal reservoir with continent diversion as definitive treatment. Canadian Urological Association Journal, 9(3-4), e142–4. https://doi.org/10.5489/cuaj.2534

Issue

Section

Case Report