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Zinner Syndrome with Papillary Neoplasm: A Rare Case Report
One of the uncommon urogenital malformations in males, which presents late in the second or third decades of life, is the congenital malformation of the seminal vesicle. Zinner syndrome is a rare condition comprising a triad of unilateral renal agenesis, ipsilateral seminal vesicle obstruction, and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9552633/ https://www.ncbi.nlm.nih.gov/pubmed/36238315 http://dx.doi.org/10.4103/jiaps.jiaps_84_21 |
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author | Randhawa, Jaskiran S. Shankaran, R. Nagamahendran, R. Upadhye, Manoj Arun Deepak, H |
author_facet | Randhawa, Jaskiran S. Shankaran, R. Nagamahendran, R. Upadhye, Manoj Arun Deepak, H |
author_sort | Randhawa, Jaskiran S. |
collection | PubMed |
description | One of the uncommon urogenital malformations in males, which presents late in the second or third decades of life, is the congenital malformation of the seminal vesicle. Zinner syndrome is a rare condition comprising a triad of unilateral renal agenesis, ipsilateral seminal vesicle obstruction, and ipsilateral ejaculatory duct obstruction. Very few cases in the literature describe the malignant change in seminal vesicle cyst in Zinner syndrome. To the best of our knowledge, this is the first report of a papillary neoplasm of the seminal vesicle cyst developed in a patient with Zinner syndrome. |
format | Online Article Text |
id | pubmed-9552633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-95526332022-10-12 Zinner Syndrome with Papillary Neoplasm: A Rare Case Report Randhawa, Jaskiran S. Shankaran, R. Nagamahendran, R. Upadhye, Manoj Arun Deepak, H J Indian Assoc Pediatr Surg Case Report One of the uncommon urogenital malformations in males, which presents late in the second or third decades of life, is the congenital malformation of the seminal vesicle. Zinner syndrome is a rare condition comprising a triad of unilateral renal agenesis, ipsilateral seminal vesicle obstruction, and ipsilateral ejaculatory duct obstruction. Very few cases in the literature describe the malignant change in seminal vesicle cyst in Zinner syndrome. To the best of our knowledge, this is the first report of a papillary neoplasm of the seminal vesicle cyst developed in a patient with Zinner syndrome. Wolters Kluwer - Medknow 2022 2022-07-26 /pmc/articles/PMC9552633/ /pubmed/36238315 http://dx.doi.org/10.4103/jiaps.jiaps_84_21 Text en Copyright: © 2022 Journal of Indian Association of Pediatric Surgeons 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 Randhawa, Jaskiran S. Shankaran, R. Nagamahendran, R. Upadhye, Manoj Arun Deepak, H Zinner Syndrome with Papillary Neoplasm: A Rare Case Report |
title | Zinner Syndrome with Papillary Neoplasm: A Rare Case Report |
title_full | Zinner Syndrome with Papillary Neoplasm: A Rare Case Report |
title_fullStr | Zinner Syndrome with Papillary Neoplasm: A Rare Case Report |
title_full_unstemmed | Zinner Syndrome with Papillary Neoplasm: A Rare Case Report |
title_short | Zinner Syndrome with Papillary Neoplasm: A Rare Case Report |
title_sort | zinner syndrome with papillary neoplasm: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9552633/ https://www.ncbi.nlm.nih.gov/pubmed/36238315 http://dx.doi.org/10.4103/jiaps.jiaps_84_21 |
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