Concurrent Multicystic Dysplastic Kidney, Posterior Urethral Valves, and Obstructive Ureterocele in a Male Pediatric Patient: A Case Report

Kurt Willis, Dawn L. MacLellan, Rodrigo L.P. Romao, Daniel T. Keefe

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

Resumen

Congenital anomalies of the kidney and urinary tract (CAKUT) are diagnosed in approximately 3-6 per 1000 live births and represent a spectrum of urologic conditions impacting the kidneys, ureter, bladder, and urethra.1 Although both are considered under the classification of CAKUT, there is no known unifying pathophysiologic mechanism for ureteroceles and posterior urethral valves with only 1 case report noted in the literature. Herein we report the only documented case of a patient with CAKUT related to posterior urethral valves, ureterocele, and multicystic dysplastic kidney.

Idioma originalEnglish
PublicaciónUrology
DOI
EstadoAccepted/In press - 2022

Nota bibliográfica

Publisher Copyright:
© 2022 Elsevier Inc.

ASJC Scopus Subject Areas

  • Urology

PubMed: MeSH publication types

  • Case Reports

Huella

Profundice en los temas de investigación de 'Concurrent Multicystic Dysplastic Kidney, Posterior Urethral Valves, and Obstructive Ureterocele in a Male Pediatric Patient: A Case Report'. En conjunto forman una huella única.

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