Cargando…

A Rare Location and Presentation of Pheochromocytoma

Background: Pheochromocytomas typically are diagnosed in the adrenal gland and from the sympathetic nervous system. Bladder pheochromocytoma is a rare location for this tumor. Case Presentation: We describe a 67-year-old Afro Caribbean woman referred to our hospital for an asymptomatic bladder tumor...

Descripción completa

Detalles Bibliográficos
Autores principales: Kaulanjan, Kevin, Blanchet, Pascal, Brureau, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6059067/
https://www.ncbi.nlm.nih.gov/pubmed/30065958
http://dx.doi.org/10.1089/cren.2018.0025
_version_ 1783341812690190336
author Kaulanjan, Kevin
Blanchet, Pascal
Brureau, Laurent
author_facet Kaulanjan, Kevin
Blanchet, Pascal
Brureau, Laurent
author_sort Kaulanjan, Kevin
collection PubMed
description Background: Pheochromocytomas typically are diagnosed in the adrenal gland and from the sympathetic nervous system. Bladder pheochromocytoma is a rare location for this tumor. Case Presentation: We describe a 67-year-old Afro Caribbean woman referred to our hospital for an asymptomatic bladder tumor. Preliminary transurethral resection revealed bladder pheochromocytoma. After a comprehensive endocrine evaluation, we performed a robot-assisted laparoscopic partial cystectomy with ureteral reimplantation. Conclusion: We present a rare case of bladder pheochromocytoma treated effectively with minimally invasive techniques. When confronted with a solid bladder mass, apart from the more common urothelial malignancies, a differential diagnosis of bladder pheochromocytoma should also be considered.
format Online
Article
Text
id pubmed-6059067
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Mary Ann Liebert, Inc.
record_format MEDLINE/PubMed
spelling pubmed-60590672018-07-31 A Rare Location and Presentation of Pheochromocytoma Kaulanjan, Kevin Blanchet, Pascal Brureau, Laurent J Endourol Case Rep Article Background: Pheochromocytomas typically are diagnosed in the adrenal gland and from the sympathetic nervous system. Bladder pheochromocytoma is a rare location for this tumor. Case Presentation: We describe a 67-year-old Afro Caribbean woman referred to our hospital for an asymptomatic bladder tumor. Preliminary transurethral resection revealed bladder pheochromocytoma. After a comprehensive endocrine evaluation, we performed a robot-assisted laparoscopic partial cystectomy with ureteral reimplantation. Conclusion: We present a rare case of bladder pheochromocytoma treated effectively with minimally invasive techniques. When confronted with a solid bladder mass, apart from the more common urothelial malignancies, a differential diagnosis of bladder pheochromocytoma should also be considered. Mary Ann Liebert, Inc. 2018-07-01 /pmc/articles/PMC6059067/ /pubmed/30065958 http://dx.doi.org/10.1089/cren.2018.0025 Text en © Kevin Kaulanjan et al. 2018; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Kaulanjan, Kevin
Blanchet, Pascal
Brureau, Laurent
A Rare Location and Presentation of Pheochromocytoma
title A Rare Location and Presentation of Pheochromocytoma
title_full A Rare Location and Presentation of Pheochromocytoma
title_fullStr A Rare Location and Presentation of Pheochromocytoma
title_full_unstemmed A Rare Location and Presentation of Pheochromocytoma
title_short A Rare Location and Presentation of Pheochromocytoma
title_sort rare location and presentation of pheochromocytoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6059067/
https://www.ncbi.nlm.nih.gov/pubmed/30065958
http://dx.doi.org/10.1089/cren.2018.0025
work_keys_str_mv AT kaulanjankevin ararelocationandpresentationofpheochromocytoma
AT blanchetpascal ararelocationandpresentationofpheochromocytoma
AT brureaulaurent ararelocationandpresentationofpheochromocytoma
AT kaulanjankevin rarelocationandpresentationofpheochromocytoma
AT blanchetpascal rarelocationandpresentationofpheochromocytoma
AT brureaulaurent rarelocationandpresentationofpheochromocytoma