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Rare presentation of growing teratoma syndrome in patient with remote history of testicular cancer resection
Growing teratoma syndrome (GTS) is documented in literature to be a rare complication of non-seminomatous germ cell tumors that arises following chemotherapeutic treatment. Though represented through multiple case reports, the condition is rare that it evades observation and diagnosis, leading to co...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7849954/ https://www.ncbi.nlm.nih.gov/pubmed/33542815 http://dx.doi.org/10.1093/jscr/rjaa600 |
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author | Nelson, Blessie Warfield, Dylan Mejia, Camilo Velasquez Walker, John Patrick |
author_facet | Nelson, Blessie Warfield, Dylan Mejia, Camilo Velasquez Walker, John Patrick |
author_sort | Nelson, Blessie |
collection | PubMed |
description | Growing teratoma syndrome (GTS) is documented in literature to be a rare complication of non-seminomatous germ cell tumors that arises following chemotherapeutic treatment. Though represented through multiple case reports, the condition is rare that it evades observation and diagnosis, leading to complications secondary to metastasis and unchecked growth. GTS is identified via incidental finding on imaging (e.g. CT) or due to complications involving mass obstruction. Due to the potential severity of undiagnosed malignancy, it is important to effectively diagnose GTS in those presenting with non-specific symptoms and a history of testicular/ovarian cancer. It is also necessary to develop a method on how to monitor those considered to be at increased risk for developing such a condition. Here, we present a case of a middle-aged male who presented with complaints of a left lower quadrant abdominal mass and incidental finding of right retroperitoneal lesion, consistent with GTS. |
format | Online Article Text |
id | pubmed-7849954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-78499542021-02-03 Rare presentation of growing teratoma syndrome in patient with remote history of testicular cancer resection Nelson, Blessie Warfield, Dylan Mejia, Camilo Velasquez Walker, John Patrick J Surg Case Rep Case Report Growing teratoma syndrome (GTS) is documented in literature to be a rare complication of non-seminomatous germ cell tumors that arises following chemotherapeutic treatment. Though represented through multiple case reports, the condition is rare that it evades observation and diagnosis, leading to complications secondary to metastasis and unchecked growth. GTS is identified via incidental finding on imaging (e.g. CT) or due to complications involving mass obstruction. Due to the potential severity of undiagnosed malignancy, it is important to effectively diagnose GTS in those presenting with non-specific symptoms and a history of testicular/ovarian cancer. It is also necessary to develop a method on how to monitor those considered to be at increased risk for developing such a condition. Here, we present a case of a middle-aged male who presented with complaints of a left lower quadrant abdominal mass and incidental finding of right retroperitoneal lesion, consistent with GTS. Oxford University Press 2021-01-29 /pmc/articles/PMC7849954/ /pubmed/33542815 http://dx.doi.org/10.1093/jscr/rjaa600 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2021. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Case Report Nelson, Blessie Warfield, Dylan Mejia, Camilo Velasquez Walker, John Patrick Rare presentation of growing teratoma syndrome in patient with remote history of testicular cancer resection |
title | Rare presentation of growing teratoma syndrome in patient with remote history of testicular cancer resection |
title_full | Rare presentation of growing teratoma syndrome in patient with remote history of testicular cancer resection |
title_fullStr | Rare presentation of growing teratoma syndrome in patient with remote history of testicular cancer resection |
title_full_unstemmed | Rare presentation of growing teratoma syndrome in patient with remote history of testicular cancer resection |
title_short | Rare presentation of growing teratoma syndrome in patient with remote history of testicular cancer resection |
title_sort | rare presentation of growing teratoma syndrome in patient with remote history of testicular cancer resection |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7849954/ https://www.ncbi.nlm.nih.gov/pubmed/33542815 http://dx.doi.org/10.1093/jscr/rjaa600 |
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