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Zinner's syndrome: Case report of a rare maldevelopment in the male genitourinary tract

Zinner syndrome is a rare congenital malformation of the urogenital tract. It is due anomaly in the developmental of Wolffian duct. Zinner syndrome comprises triad of seminal vesicle cyst, unilateral renal agenesis and ipsilateral ejaculatory duct obstruction. It is frequently associated with infert...

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Autores principales: Almuhanna, Ahmed M., Alsuhaibani, Shaheed, Almesned, Razan, Almatar, Ashraf, Alali, Hamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455976/
https://www.ncbi.nlm.nih.gov/pubmed/34584848
http://dx.doi.org/10.1016/j.eucr.2021.101839
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author Almuhanna, Ahmed M.
Alsuhaibani, Shaheed
Almesned, Razan
Almatar, Ashraf
Alali, Hamed
author_facet Almuhanna, Ahmed M.
Alsuhaibani, Shaheed
Almesned, Razan
Almatar, Ashraf
Alali, Hamed
author_sort Almuhanna, Ahmed M.
collection PubMed
description Zinner syndrome is a rare congenital malformation of the urogenital tract. It is due anomaly in the developmental of Wolffian duct. Zinner syndrome comprises triad of seminal vesicle cyst, unilateral renal agenesis and ipsilateral ejaculatory duct obstruction. It is frequently associated with infertility. Herein we are highlighting a case of a 35 years-old male, a father of 4 biological children who presented to our clinic due to right hemiscrotal pain, associated with post ejaculation pain.
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spelling pubmed-84559762021-09-27 Zinner's syndrome: Case report of a rare maldevelopment in the male genitourinary tract Almuhanna, Ahmed M. Alsuhaibani, Shaheed Almesned, Razan Almatar, Ashraf Alali, Hamed Urol Case Rep Endrology & Infertility Zinner syndrome is a rare congenital malformation of the urogenital tract. It is due anomaly in the developmental of Wolffian duct. Zinner syndrome comprises triad of seminal vesicle cyst, unilateral renal agenesis and ipsilateral ejaculatory duct obstruction. It is frequently associated with infertility. Herein we are highlighting a case of a 35 years-old male, a father of 4 biological children who presented to our clinic due to right hemiscrotal pain, associated with post ejaculation pain. Elsevier 2021-09-14 /pmc/articles/PMC8455976/ /pubmed/34584848 http://dx.doi.org/10.1016/j.eucr.2021.101839 Text en © 2021 The Authors. Published by Elsevier Inc. 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 Endrology & Infertility
Almuhanna, Ahmed M.
Alsuhaibani, Shaheed
Almesned, Razan
Almatar, Ashraf
Alali, Hamed
Zinner's syndrome: Case report of a rare maldevelopment in the male genitourinary tract
title Zinner's syndrome: Case report of a rare maldevelopment in the male genitourinary tract
title_full Zinner's syndrome: Case report of a rare maldevelopment in the male genitourinary tract
title_fullStr Zinner's syndrome: Case report of a rare maldevelopment in the male genitourinary tract
title_full_unstemmed Zinner's syndrome: Case report of a rare maldevelopment in the male genitourinary tract
title_short Zinner's syndrome: Case report of a rare maldevelopment in the male genitourinary tract
title_sort zinner's syndrome: case report of a rare maldevelopment in the male genitourinary tract
topic Endrology & Infertility
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455976/
https://www.ncbi.nlm.nih.gov/pubmed/34584848
http://dx.doi.org/10.1016/j.eucr.2021.101839
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