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Zinner Syndrome: A Case Report of Rare Urogenital Anomaly

Zinner Syndrome is a rare urogenital tract anomaly with unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ipsilateral ejaculatory duct obstruction. The syndrome occurs due to an insult to the development of the paramesonephric duct during embryogenesis. Patients may present late due t...

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Detalles Bibliográficos
Autores principales: Gurung, Bibek, Panta, Om Biju, Dhakal, Vivek, Ghimire, Ram Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9030355/
https://www.ncbi.nlm.nih.gov/pubmed/35465594
http://dx.doi.org/10.4103/JMU.JMU_125_20
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author Gurung, Bibek
Panta, Om Biju
Dhakal, Vivek
Ghimire, Ram Kumar
author_facet Gurung, Bibek
Panta, Om Biju
Dhakal, Vivek
Ghimire, Ram Kumar
author_sort Gurung, Bibek
collection PubMed
description Zinner Syndrome is a rare urogenital tract anomaly with unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ipsilateral ejaculatory duct obstruction. The syndrome occurs due to an insult to the development of the paramesonephric duct during embryogenesis. Patients may present late due to dysejaculation as a result of obstruction of the ejaculatory duct or commonly remain asymptomatic. Here, we present such a case presenting with dysejaculation which was diagnosed with Zinner syndrome on ultrasound.
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spelling pubmed-90303552022-04-23 Zinner Syndrome: A Case Report of Rare Urogenital Anomaly Gurung, Bibek Panta, Om Biju Dhakal, Vivek Ghimire, Ram Kumar J Med Ultrasound Case Report Zinner Syndrome is a rare urogenital tract anomaly with unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ipsilateral ejaculatory duct obstruction. The syndrome occurs due to an insult to the development of the paramesonephric duct during embryogenesis. Patients may present late due to dysejaculation as a result of obstruction of the ejaculatory duct or commonly remain asymptomatic. Here, we present such a case presenting with dysejaculation which was diagnosed with Zinner syndrome on ultrasound. Wolters Kluwer - Medknow 2021-05-04 /pmc/articles/PMC9030355/ /pubmed/35465594 http://dx.doi.org/10.4103/JMU.JMU_125_20 Text en Copyright: © 2021 Journal of Medical Ultrasound 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
Gurung, Bibek
Panta, Om Biju
Dhakal, Vivek
Ghimire, Ram Kumar
Zinner Syndrome: A Case Report of Rare Urogenital Anomaly
title Zinner Syndrome: A Case Report of Rare Urogenital Anomaly
title_full Zinner Syndrome: A Case Report of Rare Urogenital Anomaly
title_fullStr Zinner Syndrome: A Case Report of Rare Urogenital Anomaly
title_full_unstemmed Zinner Syndrome: A Case Report of Rare Urogenital Anomaly
title_short Zinner Syndrome: A Case Report of Rare Urogenital Anomaly
title_sort zinner syndrome: a case report of rare urogenital anomaly
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9030355/
https://www.ncbi.nlm.nih.gov/pubmed/35465594
http://dx.doi.org/10.4103/JMU.JMU_125_20
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