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Pheochromocytoma Presenting as Testicular Pain: An Unusual Case Report

Pheochromocytoma (PCC) is a rare catecholamine-secreting tumor that arises from chromaffin cells of the adrenal medulla which are derived from the neural crest. This report illustrates a 51-year-old Caucasian male with a history of hypertension diagnosed two years ago who presented to the hospital d...

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Autores principales: Patel, Jinal K., Reddy, Varun, Stepman, Gauthier, Angelo, Debra, Frunzi, Johnathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062206/
https://www.ncbi.nlm.nih.gov/pubmed/33953991
http://dx.doi.org/10.1155/2021/6699409
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author Patel, Jinal K.
Reddy, Varun
Stepman, Gauthier
Angelo, Debra
Frunzi, Johnathan
author_facet Patel, Jinal K.
Reddy, Varun
Stepman, Gauthier
Angelo, Debra
Frunzi, Johnathan
author_sort Patel, Jinal K.
collection PubMed
description Pheochromocytoma (PCC) is a rare catecholamine-secreting tumor that arises from chromaffin cells of the adrenal medulla which are derived from the neural crest. This report illustrates a 51-year-old Caucasian male with a history of hypertension diagnosed two years ago who presented to the hospital due to acute onset of right testicular pain of 3-day duration. Laboratory results and imaging revealed a presumptive diagnosis of PCC. The patient had undergone robot-assisted laparoscopic right adrenalectomy 14 days after being diagnosed with PCC due to perioperative management with phenoxybenzamine. The final pathology report revealed a PCC. At follow-up two weeks after discharge, the patient reported complete resolution of his testicular pain.
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spelling pubmed-80622062021-05-04 Pheochromocytoma Presenting as Testicular Pain: An Unusual Case Report Patel, Jinal K. Reddy, Varun Stepman, Gauthier Angelo, Debra Frunzi, Johnathan Case Rep Endocrinol Case Report Pheochromocytoma (PCC) is a rare catecholamine-secreting tumor that arises from chromaffin cells of the adrenal medulla which are derived from the neural crest. This report illustrates a 51-year-old Caucasian male with a history of hypertension diagnosed two years ago who presented to the hospital due to acute onset of right testicular pain of 3-day duration. Laboratory results and imaging revealed a presumptive diagnosis of PCC. The patient had undergone robot-assisted laparoscopic right adrenalectomy 14 days after being diagnosed with PCC due to perioperative management with phenoxybenzamine. The final pathology report revealed a PCC. At follow-up two weeks after discharge, the patient reported complete resolution of his testicular pain. Hindawi 2021-04-14 /pmc/articles/PMC8062206/ /pubmed/33953991 http://dx.doi.org/10.1155/2021/6699409 Text en Copyright © 2021 Jinal K. Patel et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Patel, Jinal K.
Reddy, Varun
Stepman, Gauthier
Angelo, Debra
Frunzi, Johnathan
Pheochromocytoma Presenting as Testicular Pain: An Unusual Case Report
title Pheochromocytoma Presenting as Testicular Pain: An Unusual Case Report
title_full Pheochromocytoma Presenting as Testicular Pain: An Unusual Case Report
title_fullStr Pheochromocytoma Presenting as Testicular Pain: An Unusual Case Report
title_full_unstemmed Pheochromocytoma Presenting as Testicular Pain: An Unusual Case Report
title_short Pheochromocytoma Presenting as Testicular Pain: An Unusual Case Report
title_sort pheochromocytoma presenting as testicular pain: an unusual case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062206/
https://www.ncbi.nlm.nih.gov/pubmed/33953991
http://dx.doi.org/10.1155/2021/6699409
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