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Symptomatic paraganglioma of the urinary bladder: A rare case treated with a combined surgical approach
Pheochromocytomas are tumors of the embryonic chromaffin cells, originating from the embryonic neural crest. The pheochromocytomas developing at extra-adrenal locations are termed paragangliomas, which are extremely rare and account for almost 0.06% of all bladder tumors. In this report, we present...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267705/ https://www.ncbi.nlm.nih.gov/pubmed/32514405 http://dx.doi.org/10.1016/j.eucr.2020.101290 |
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author | Sonmez, Gokhan Tombul, Sevket Tolga Golbasi, Abdullah Demirtas, Turev Akgun, Hulya Demirtas, Abdullah |
author_facet | Sonmez, Gokhan Tombul, Sevket Tolga Golbasi, Abdullah Demirtas, Turev Akgun, Hulya Demirtas, Abdullah |
author_sort | Sonmez, Gokhan |
collection | PubMed |
description | Pheochromocytomas are tumors of the embryonic chromaffin cells, originating from the embryonic neural crest. The pheochromocytomas developing at extra-adrenal locations are termed paragangliomas, which are extremely rare and account for almost 0.06% of all bladder tumors. In this report, we present a 23-year-old woman who presented with a one-year history of repeated episodes of dizziness, hypertension, intermittent hematuria, and nausea/vomiting that occurred during urination and was operatively treated due to a diagnosis of paraganglioma of the urinary bladder. |
format | Online Article Text |
id | pubmed-7267705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-72677052020-06-07 Symptomatic paraganglioma of the urinary bladder: A rare case treated with a combined surgical approach Sonmez, Gokhan Tombul, Sevket Tolga Golbasi, Abdullah Demirtas, Turev Akgun, Hulya Demirtas, Abdullah Urol Case Rep Oncology Pheochromocytomas are tumors of the embryonic chromaffin cells, originating from the embryonic neural crest. The pheochromocytomas developing at extra-adrenal locations are termed paragangliomas, which are extremely rare and account for almost 0.06% of all bladder tumors. In this report, we present a 23-year-old woman who presented with a one-year history of repeated episodes of dizziness, hypertension, intermittent hematuria, and nausea/vomiting that occurred during urination and was operatively treated due to a diagnosis of paraganglioma of the urinary bladder. Elsevier 2020-05-29 /pmc/articles/PMC7267705/ /pubmed/32514405 http://dx.doi.org/10.1016/j.eucr.2020.101290 Text en © 2020 Published by Elsevier Inc. 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 | Oncology Sonmez, Gokhan Tombul, Sevket Tolga Golbasi, Abdullah Demirtas, Turev Akgun, Hulya Demirtas, Abdullah Symptomatic paraganglioma of the urinary bladder: A rare case treated with a combined surgical approach |
title | Symptomatic paraganglioma of the urinary bladder: A rare case treated with a combined surgical approach |
title_full | Symptomatic paraganglioma of the urinary bladder: A rare case treated with a combined surgical approach |
title_fullStr | Symptomatic paraganglioma of the urinary bladder: A rare case treated with a combined surgical approach |
title_full_unstemmed | Symptomatic paraganglioma of the urinary bladder: A rare case treated with a combined surgical approach |
title_short | Symptomatic paraganglioma of the urinary bladder: A rare case treated with a combined surgical approach |
title_sort | symptomatic paraganglioma of the urinary bladder: a rare case treated with a combined surgical approach |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267705/ https://www.ncbi.nlm.nih.gov/pubmed/32514405 http://dx.doi.org/10.1016/j.eucr.2020.101290 |
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