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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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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. |
format | Online Article Text |
id | pubmed-9030355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
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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