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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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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. |
format | Online Article Text |
id | pubmed-8455976 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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