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Type IIB urethral duplication in adult: A case report

Urethral duplication are rare anomalies of the lower urinary tract consisting of partial or complete development of an accessory urethra that common in males than female. The exact embryological mechanism for this condition remain unclear, it is thought to relate to a disruption of development of th...

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Detalles Bibliográficos
Autores principales: Dewi, Dian Komala, Gunawan, Cristha Octaviani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238602/
https://www.ncbi.nlm.nih.gov/pubmed/37273733
http://dx.doi.org/10.1016/j.radcr.2023.04.036
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author Dewi, Dian Komala
Gunawan, Cristha Octaviani
author_facet Dewi, Dian Komala
Gunawan, Cristha Octaviani
author_sort Dewi, Dian Komala
collection PubMed
description Urethral duplication are rare anomalies of the lower urinary tract consisting of partial or complete development of an accessory urethra that common in males than female. The exact embryological mechanism for this condition remain unclear, it is thought to relate to a disruption of development of the lateral folds of Rathke during hindgut development. There are 3 types based on Effman's classification. Diagnosis of urethral duplication, a genital examination has to performed and confirmed by micturating cytourethrography and retrograde urethrography. The authors presented a case of 67-year-old man complaining of dysuria, who was diagnosed with urethral duplication Effman Classification type IIB accompanied by bulbar urethral stricture and diverticula and multiple bladder diverticula after performing retrograde urethrography and micturating cystourethrography. This is an extremely rare type of duplication of the urethra (type IIB) with late presentation. Further study may be required regarding the surgical management.
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spelling pubmed-102386022023-06-04 Type IIB urethral duplication in adult: A case report Dewi, Dian Komala Gunawan, Cristha Octaviani Radiol Case Rep Case Report Urethral duplication are rare anomalies of the lower urinary tract consisting of partial or complete development of an accessory urethra that common in males than female. The exact embryological mechanism for this condition remain unclear, it is thought to relate to a disruption of development of the lateral folds of Rathke during hindgut development. There are 3 types based on Effman's classification. Diagnosis of urethral duplication, a genital examination has to performed and confirmed by micturating cytourethrography and retrograde urethrography. The authors presented a case of 67-year-old man complaining of dysuria, who was diagnosed with urethral duplication Effman Classification type IIB accompanied by bulbar urethral stricture and diverticula and multiple bladder diverticula after performing retrograde urethrography and micturating cystourethrography. This is an extremely rare type of duplication of the urethra (type IIB) with late presentation. Further study may be required regarding the surgical management. Elsevier 2023-05-26 /pmc/articles/PMC10238602/ /pubmed/37273733 http://dx.doi.org/10.1016/j.radcr.2023.04.036 Text en © 2023 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://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 Case Report
Dewi, Dian Komala
Gunawan, Cristha Octaviani
Type IIB urethral duplication in adult: A case report
title Type IIB urethral duplication in adult: A case report
title_full Type IIB urethral duplication in adult: A case report
title_fullStr Type IIB urethral duplication in adult: A case report
title_full_unstemmed Type IIB urethral duplication in adult: A case report
title_short Type IIB urethral duplication in adult: A case report
title_sort type iib urethral duplication in adult: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238602/
https://www.ncbi.nlm.nih.gov/pubmed/37273733
http://dx.doi.org/10.1016/j.radcr.2023.04.036
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