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Congenital anterior urethral diverticula with posterior urethral valve: A rare combination, case report()

BACKGROUND: Congenital anterior urethral diverticulum is a rare cause of urinary obstruction in children. Its association with posterior urethral valve is an exceedingly unusual occurrence. CASE PRESENTATION: 18 month old male child for whom cystoscopic valve ablation was done for posterior urethral...

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Detalles Bibliográficos
Autores principales: Abebe, Hana, Girma, Hiwote, Temesgen, Fisseha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568190/
https://www.ncbi.nlm.nih.gov/pubmed/33094095
http://dx.doi.org/10.1016/j.eucr.2020.101447
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author Abebe, Hana
Girma, Hiwote
Temesgen, Fisseha
author_facet Abebe, Hana
Girma, Hiwote
Temesgen, Fisseha
author_sort Abebe, Hana
collection PubMed
description BACKGROUND: Congenital anterior urethral diverticulum is a rare cause of urinary obstruction in children. Its association with posterior urethral valve is an exceedingly unusual occurrence. CASE PRESENTATION: 18 month old male child for whom cystoscopic valve ablation was done for posterior urethral valve continued to have obstructive symptoms for which VCUG was done and revealed congenital anterior urethral diverticula. Open diverticulectomy and urethroplasty was done and he was discharged improved. CONCLUSION: This case report represents a rare event in which two congenital causes of bladder outlet obstruction are combined and the presence of one masquaders the diagnosis of the other.
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spelling pubmed-75681902020-10-21 Congenital anterior urethral diverticula with posterior urethral valve: A rare combination, case report() Abebe, Hana Girma, Hiwote Temesgen, Fisseha Urol Case Rep Pediatrics BACKGROUND: Congenital anterior urethral diverticulum is a rare cause of urinary obstruction in children. Its association with posterior urethral valve is an exceedingly unusual occurrence. CASE PRESENTATION: 18 month old male child for whom cystoscopic valve ablation was done for posterior urethral valve continued to have obstructive symptoms for which VCUG was done and revealed congenital anterior urethral diverticula. Open diverticulectomy and urethroplasty was done and he was discharged improved. CONCLUSION: This case report represents a rare event in which two congenital causes of bladder outlet obstruction are combined and the presence of one masquaders the diagnosis of the other. Elsevier 2020-10-12 /pmc/articles/PMC7568190/ /pubmed/33094095 http://dx.doi.org/10.1016/j.eucr.2020.101447 Text en © 2020 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Pediatrics
Abebe, Hana
Girma, Hiwote
Temesgen, Fisseha
Congenital anterior urethral diverticula with posterior urethral valve: A rare combination, case report()
title Congenital anterior urethral diverticula with posterior urethral valve: A rare combination, case report()
title_full Congenital anterior urethral diverticula with posterior urethral valve: A rare combination, case report()
title_fullStr Congenital anterior urethral diverticula with posterior urethral valve: A rare combination, case report()
title_full_unstemmed Congenital anterior urethral diverticula with posterior urethral valve: A rare combination, case report()
title_short Congenital anterior urethral diverticula with posterior urethral valve: A rare combination, case report()
title_sort congenital anterior urethral diverticula with posterior urethral valve: a rare combination, case report()
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568190/
https://www.ncbi.nlm.nih.gov/pubmed/33094095
http://dx.doi.org/10.1016/j.eucr.2020.101447
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