Bladder Agenesis and Bilateral Ectopic Ureters in an Infant Male With Cystic Renal Dysplasia, Imperforate Anus, and Penoscrotal Transposition - 30/10/21
Abstract |
Bladder agenesis is a rare congenital anomaly infrequently reported in the literature, with an incidence of 1/600,000 patients.1 Commonly associated with other fatal malformations, the condition is often incompatible with life.2 Prior reports estimate that over 90% of living children born with this malformation are female, owing to renal preservation resulting from low pressure drainage of urine into the vagina, uterus, and vestibule.3,4 Herein we report a rare case of an infant male born with penoscrotal transposition and end stage renal disease secondary to bilateral cystic renal dysplasia found to have concurrent bladder agenesis and bilateral ureteral ectopia.
Le texte complet de cet article est disponible en PDF.Abbreviations : MRI, NICU, BMI, PKD, VCUG, DOL, OR, HD, POD
Plan
Vol 156
P. 256-259 - octobre 2021 Retour au numéro
Article précédent
- Magnetic Double-J-Stent Removal Without General Anaesthesia in Children
- W. Brillat Arce, R.N. Vuille-dit-Bille, S.G. Holland-Cunz, M. Frech-Doerfler
- Pediatric Robotic Adrenalectomy for Virilizing Adrenal Tumor in a 4-year-old Female
- Thomas Lowrey, David Cochran, Dominic Frimberger, Bhalaajee Meenakshi Sundaram, Shelly Mercer, Adam Rensing
Bienvenue sur EM-consulte, la référence des professionnels de santé.
L’accès au texte intégral de cet article nécessite un abonnement.
Déjà abonné à cette revue ?