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Incidental imaging findings suggesting Zinner syndrome in a young patient with pulmonary embolism: A case report

A triad of seminal vesical cyst, ipsilateral renal agenesis and ipsilateral ejaculatory duct obstruction is known as Zinner Syndrome. First described in 1914, only about 200 cases have been reported in literature. Usually it stays undiagnosed until the second to third decade of life due to lack of s...

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Detalles Bibliográficos
Autores principales: Hergan, Benedikt, Fellner, Franz A., Akbari, Kaveh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033301/
https://www.ncbi.nlm.nih.gov/pubmed/32148603
http://dx.doi.org/10.1016/j.radcr.2020.01.027
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author Hergan, Benedikt
Fellner, Franz A.
Akbari, Kaveh
author_facet Hergan, Benedikt
Fellner, Franz A.
Akbari, Kaveh
author_sort Hergan, Benedikt
collection PubMed
description A triad of seminal vesical cyst, ipsilateral renal agenesis and ipsilateral ejaculatory duct obstruction is known as Zinner Syndrome. First described in 1914, only about 200 cases have been reported in literature. Usually it stays undiagnosed until the second to third decade of life due to lack of symptoms or nonspecific symptoms such as lower urinary tract symptoms, dysuria or painful ejaculation. In this report we present the case of a 22-year-old patient with a Zinner syndrome as an incidental finding and underlie a review of literature to show the main clinical and imaging implications.
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spelling pubmed-70333012020-03-06 Incidental imaging findings suggesting Zinner syndrome in a young patient with pulmonary embolism: A case report Hergan, Benedikt Fellner, Franz A. Akbari, Kaveh Radiol Case Rep Genitourinary A triad of seminal vesical cyst, ipsilateral renal agenesis and ipsilateral ejaculatory duct obstruction is known as Zinner Syndrome. First described in 1914, only about 200 cases have been reported in literature. Usually it stays undiagnosed until the second to third decade of life due to lack of symptoms or nonspecific symptoms such as lower urinary tract symptoms, dysuria or painful ejaculation. In this report we present the case of a 22-year-old patient with a Zinner syndrome as an incidental finding and underlie a review of literature to show the main clinical and imaging implications. Elsevier 2020-02-19 /pmc/articles/PMC7033301/ /pubmed/32148603 http://dx.doi.org/10.1016/j.radcr.2020.01.027 Text en © 2020 The Authors. Published by Elsevier Inc. on behalf of University of Washington. http://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 Genitourinary
Hergan, Benedikt
Fellner, Franz A.
Akbari, Kaveh
Incidental imaging findings suggesting Zinner syndrome in a young patient with pulmonary embolism: A case report
title Incidental imaging findings suggesting Zinner syndrome in a young patient with pulmonary embolism: A case report
title_full Incidental imaging findings suggesting Zinner syndrome in a young patient with pulmonary embolism: A case report
title_fullStr Incidental imaging findings suggesting Zinner syndrome in a young patient with pulmonary embolism: A case report
title_full_unstemmed Incidental imaging findings suggesting Zinner syndrome in a young patient with pulmonary embolism: A case report
title_short Incidental imaging findings suggesting Zinner syndrome in a young patient with pulmonary embolism: A case report
title_sort incidental imaging findings suggesting zinner syndrome in a young patient with pulmonary embolism: a case report
topic Genitourinary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033301/
https://www.ncbi.nlm.nih.gov/pubmed/32148603
http://dx.doi.org/10.1016/j.radcr.2020.01.027
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