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Bladder paraganglioma after kidney transplantation: A case report
BACKGROUND: Kidney transplantation is associated with an increased risk of tumors in the urinary bladder. Among all the pathological types of tumors in the bladder, paraganglioma, which arises from extra-adrenal paraganglia and consists of chromaffin cells, is rare. Paragangliomas might cause severe...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477062/ https://www.ncbi.nlm.nih.gov/pubmed/36157666 http://dx.doi.org/10.12998/wjcc.v10.i25.9044 |
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author | Wang, Lin Zhang, Yan-Ning Chen, Guang-Yong |
author_facet | Wang, Lin Zhang, Yan-Ning Chen, Guang-Yong |
author_sort | Wang, Lin |
collection | PubMed |
description | BACKGROUND: Kidney transplantation is associated with an increased risk of tumors in the urinary bladder. Among all the pathological types of tumors in the bladder, paraganglioma, which arises from extra-adrenal paraganglia and consists of chromaffin cells, is rare. Paragangliomas might cause severe clinical symptoms due to catecholamine hypersecretion or mass compression. Bladder paragangliomas are rare, especially those appearing after kidney transplantation. Here, we report a case of bladder paraganglioma developing after kidney transplantation. CASE SUMMARY: A 63-year-old woman received a kidney transplant 12 years ago and took oral immunosuppressants (cyclosporine, mizoribine, and methylprednisolone) for regular post-transplant treatment. The patient felt no discomfort and she came to the hospital for a routine checkup. A mass located in the bladder was incidentally discovered by computed tomography, and she underwent surgical treatment. A 2 cm × 2 cm invasive mass was found in the trigone of the bladder and the mass was removed. The diagnosis of paraganglioma was confirmed by morphology and immunophenotyping. The patient had a good prognosis and is still alive. CONCLUSION: Paraganglioma can grow in the bladder, which might cause no clinical symptoms. The diagnosis mainly depends on morphology and immunophenotyping. Surgical resection is an important treatment option for such patients. |
format | Online Article Text |
id | pubmed-9477062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-94770622022-09-23 Bladder paraganglioma after kidney transplantation: A case report Wang, Lin Zhang, Yan-Ning Chen, Guang-Yong World J Clin Cases Case Report BACKGROUND: Kidney transplantation is associated with an increased risk of tumors in the urinary bladder. Among all the pathological types of tumors in the bladder, paraganglioma, which arises from extra-adrenal paraganglia and consists of chromaffin cells, is rare. Paragangliomas might cause severe clinical symptoms due to catecholamine hypersecretion or mass compression. Bladder paragangliomas are rare, especially those appearing after kidney transplantation. Here, we report a case of bladder paraganglioma developing after kidney transplantation. CASE SUMMARY: A 63-year-old woman received a kidney transplant 12 years ago and took oral immunosuppressants (cyclosporine, mizoribine, and methylprednisolone) for regular post-transplant treatment. The patient felt no discomfort and she came to the hospital for a routine checkup. A mass located in the bladder was incidentally discovered by computed tomography, and she underwent surgical treatment. A 2 cm × 2 cm invasive mass was found in the trigone of the bladder and the mass was removed. The diagnosis of paraganglioma was confirmed by morphology and immunophenotyping. The patient had a good prognosis and is still alive. CONCLUSION: Paraganglioma can grow in the bladder, which might cause no clinical symptoms. The diagnosis mainly depends on morphology and immunophenotyping. Surgical resection is an important treatment option for such patients. Baishideng Publishing Group Inc 2022-09-06 2022-09-06 /pmc/articles/PMC9477062/ /pubmed/36157666 http://dx.doi.org/10.12998/wjcc.v10.i25.9044 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Case Report Wang, Lin Zhang, Yan-Ning Chen, Guang-Yong Bladder paraganglioma after kidney transplantation: A case report |
title | Bladder paraganglioma after kidney transplantation: A case report |
title_full | Bladder paraganglioma after kidney transplantation: A case report |
title_fullStr | Bladder paraganglioma after kidney transplantation: A case report |
title_full_unstemmed | Bladder paraganglioma after kidney transplantation: A case report |
title_short | Bladder paraganglioma after kidney transplantation: A case report |
title_sort | bladder paraganglioma after kidney transplantation: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477062/ https://www.ncbi.nlm.nih.gov/pubmed/36157666 http://dx.doi.org/10.12998/wjcc.v10.i25.9044 |
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