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Bilateral Adrenal Incidentalomas: A Case Report and Review of Diagnostic Challenges

Incidentally discovered adrenal masses (incidentalomas) are common and present challenges both in diagnosis and management. When incidentally discovered adrenal masses are bilateral, a refined diagnostic approach is warranted since bilateral disease is more likely to be pathologic. We review a case...

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Detalles Bibliográficos
Autores principales: Carlson, Anders L., Marney, Annis M., Anderson, Scott R., Gilbert, Matthew P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3562608/
https://www.ncbi.nlm.nih.gov/pubmed/23401807
http://dx.doi.org/10.1155/2013/953052
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author Carlson, Anders L.
Marney, Annis M.
Anderson, Scott R.
Gilbert, Matthew P.
author_facet Carlson, Anders L.
Marney, Annis M.
Anderson, Scott R.
Gilbert, Matthew P.
author_sort Carlson, Anders L.
collection PubMed
description Incidentally discovered adrenal masses (incidentalomas) are common and present challenges both in diagnosis and management. When incidentally discovered adrenal masses are bilateral, a refined diagnostic approach is warranted since bilateral disease is more likely to be pathologic. We review a case of a 34-year-old man with incidentally discovered bilateral adrenal nodules. A comprehensive diagnostic strategy led to the diagnosis of bilateral pheochromocytoma caused by von Hippel-Lindau syndrome. He was successfully treated with bilateral laparoscopic adrenalectomy and has recovered well. While the initial diagnostic approach is similar to the unilateral incidentaloma, additional testing and/or genetic testing should be considered in the case of the bilateral adrenal mass.
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spelling pubmed-35626082013-02-11 Bilateral Adrenal Incidentalomas: A Case Report and Review of Diagnostic Challenges Carlson, Anders L. Marney, Annis M. Anderson, Scott R. Gilbert, Matthew P. Case Rep Endocrinol Case Report Incidentally discovered adrenal masses (incidentalomas) are common and present challenges both in diagnosis and management. When incidentally discovered adrenal masses are bilateral, a refined diagnostic approach is warranted since bilateral disease is more likely to be pathologic. We review a case of a 34-year-old man with incidentally discovered bilateral adrenal nodules. A comprehensive diagnostic strategy led to the diagnosis of bilateral pheochromocytoma caused by von Hippel-Lindau syndrome. He was successfully treated with bilateral laparoscopic adrenalectomy and has recovered well. While the initial diagnostic approach is similar to the unilateral incidentaloma, additional testing and/or genetic testing should be considered in the case of the bilateral adrenal mass. Hindawi Publishing Corporation 2013 2013-01-17 /pmc/articles/PMC3562608/ /pubmed/23401807 http://dx.doi.org/10.1155/2013/953052 Text en Copyright © 2013 Anders L. Carlson et al. https://creativecommons.org/licenses/by/3.0/ 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
Carlson, Anders L.
Marney, Annis M.
Anderson, Scott R.
Gilbert, Matthew P.
Bilateral Adrenal Incidentalomas: A Case Report and Review of Diagnostic Challenges
title Bilateral Adrenal Incidentalomas: A Case Report and Review of Diagnostic Challenges
title_full Bilateral Adrenal Incidentalomas: A Case Report and Review of Diagnostic Challenges
title_fullStr Bilateral Adrenal Incidentalomas: A Case Report and Review of Diagnostic Challenges
title_full_unstemmed Bilateral Adrenal Incidentalomas: A Case Report and Review of Diagnostic Challenges
title_short Bilateral Adrenal Incidentalomas: A Case Report and Review of Diagnostic Challenges
title_sort bilateral adrenal incidentalomas: a case report and review of diagnostic challenges
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3562608/
https://www.ncbi.nlm.nih.gov/pubmed/23401807
http://dx.doi.org/10.1155/2013/953052
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