Cargando…

Female pseudohermaphroditism with urethral duplication: A delayed presentation in adulthood

Female pseudohermaphroditism with urethral duplication presenting as urinary retention in adulthood is extremely rare. We report the case of a 26-year-old female who had multiple failed attempts of per urethral catheterization during a planned cesarean section. She had labial fusion and clitoral hyp...

Descripción completa

Detalles Bibliográficos
Autores principales: Deshpande, Amit Vijayrao, Hazare, Jitendra D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8992713/
https://www.ncbi.nlm.nih.gov/pubmed/35400864
http://dx.doi.org/10.4103/iju.iju_401_21
_version_ 1784683784589803520
author Deshpande, Amit Vijayrao
Hazare, Jitendra D.
author_facet Deshpande, Amit Vijayrao
Hazare, Jitendra D.
author_sort Deshpande, Amit Vijayrao
collection PubMed
description Female pseudohermaphroditism with urethral duplication presenting as urinary retention in adulthood is extremely rare. We report the case of a 26-year-old female who had multiple failed attempts of per urethral catheterization during a planned cesarean section. She had labial fusion and clitoral hypertrophy with a phallic urethra and underwent labial separation with urethral reconstruction.
format Online
Article
Text
id pubmed-8992713
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Wolters Kluwer - Medknow
record_format MEDLINE/PubMed
spelling pubmed-89927132022-04-09 Female pseudohermaphroditism with urethral duplication: A delayed presentation in adulthood Deshpande, Amit Vijayrao Hazare, Jitendra D. Indian J Urol Case Report Female pseudohermaphroditism with urethral duplication presenting as urinary retention in adulthood is extremely rare. We report the case of a 26-year-old female who had multiple failed attempts of per urethral catheterization during a planned cesarean section. She had labial fusion and clitoral hypertrophy with a phallic urethra and underwent labial separation with urethral reconstruction. Wolters Kluwer - Medknow 2022 2022-04-01 /pmc/articles/PMC8992713/ /pubmed/35400864 http://dx.doi.org/10.4103/iju.iju_401_21 Text en Copyright: © 2022 Indian Journal of Urology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Deshpande, Amit Vijayrao
Hazare, Jitendra D.
Female pseudohermaphroditism with urethral duplication: A delayed presentation in adulthood
title Female pseudohermaphroditism with urethral duplication: A delayed presentation in adulthood
title_full Female pseudohermaphroditism with urethral duplication: A delayed presentation in adulthood
title_fullStr Female pseudohermaphroditism with urethral duplication: A delayed presentation in adulthood
title_full_unstemmed Female pseudohermaphroditism with urethral duplication: A delayed presentation in adulthood
title_short Female pseudohermaphroditism with urethral duplication: A delayed presentation in adulthood
title_sort female pseudohermaphroditism with urethral duplication: a delayed presentation in adulthood
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8992713/
https://www.ncbi.nlm.nih.gov/pubmed/35400864
http://dx.doi.org/10.4103/iju.iju_401_21
work_keys_str_mv AT deshpandeamitvijayrao femalepseudohermaphroditismwithurethralduplicationadelayedpresentationinadulthood
AT hazarejitendrad femalepseudohermaphroditismwithurethralduplicationadelayedpresentationinadulthood