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A Rare Adrenal Incidentaloma That Mimics Adrenocortical Carcinoma
OBJECTIVE: We present a case of an adrenal hemangioma, an uncommon cause of an adrenal mass, and review the clinical presentation, work-up, and management of adrenal incidentalomas. BACKGROUND: A 64-year-old male was found to have a right adrenal incidentaloma during work-up for elevated liver trans...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6011133/ https://www.ncbi.nlm.nih.gov/pubmed/29984033 http://dx.doi.org/10.1155/2018/9607972 |
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author | Lavingia, Kedar Torabi, Ramyar Kim, Samuel W. Hughes, Marybeth S. Feliberti, Eric C. Perry, Roger R. |
author_facet | Lavingia, Kedar Torabi, Ramyar Kim, Samuel W. Hughes, Marybeth S. Feliberti, Eric C. Perry, Roger R. |
author_sort | Lavingia, Kedar |
collection | PubMed |
description | OBJECTIVE: We present a case of an adrenal hemangioma, an uncommon cause of an adrenal mass, and review the clinical presentation, work-up, and management of adrenal incidentalomas. BACKGROUND: A 64-year-old male was found to have a right adrenal incidentaloma during work-up for elevated liver transaminase levels, later found to be from hepatitis C. The mass was suspicious for adrenocortical carcinoma on CT imaging. Biochemical evaluation revealed no evidence of function. He underwent an open right adrenalectomy. The mass was found to be an adrenal hemangioma on histopathologic analysis. METHODS: This is a case report with pertinent review of the diagnosis and management of adrenal incidentalomas. RESULTS: Adrenal hemangiomas are rare, benign, nonfunctional tumors typically found during imaging for other reasons. As illustrated by this case, they appear similar to adrenocortical carcinoma on CT imaging. The diagnosis is usually not made prior to surgical resection. CONCLUSION: Adrenal hemangioma is a rare nonfunctional adrenal incidentaloma that displays atypical features on CT imaging. The suspicion for adrenocortical carcinoma usually prompts adrenalectomy. |
format | Online Article Text |
id | pubmed-6011133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-60111332018-07-08 A Rare Adrenal Incidentaloma That Mimics Adrenocortical Carcinoma Lavingia, Kedar Torabi, Ramyar Kim, Samuel W. Hughes, Marybeth S. Feliberti, Eric C. Perry, Roger R. Case Rep Surg Case Report OBJECTIVE: We present a case of an adrenal hemangioma, an uncommon cause of an adrenal mass, and review the clinical presentation, work-up, and management of adrenal incidentalomas. BACKGROUND: A 64-year-old male was found to have a right adrenal incidentaloma during work-up for elevated liver transaminase levels, later found to be from hepatitis C. The mass was suspicious for adrenocortical carcinoma on CT imaging. Biochemical evaluation revealed no evidence of function. He underwent an open right adrenalectomy. The mass was found to be an adrenal hemangioma on histopathologic analysis. METHODS: This is a case report with pertinent review of the diagnosis and management of adrenal incidentalomas. RESULTS: Adrenal hemangiomas are rare, benign, nonfunctional tumors typically found during imaging for other reasons. As illustrated by this case, they appear similar to adrenocortical carcinoma on CT imaging. The diagnosis is usually not made prior to surgical resection. CONCLUSION: Adrenal hemangioma is a rare nonfunctional adrenal incidentaloma that displays atypical features on CT imaging. The suspicion for adrenocortical carcinoma usually prompts adrenalectomy. Hindawi 2018-06-07 /pmc/articles/PMC6011133/ /pubmed/29984033 http://dx.doi.org/10.1155/2018/9607972 Text en Copyright © 2018 Kedar Lavingia et al. http://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 Lavingia, Kedar Torabi, Ramyar Kim, Samuel W. Hughes, Marybeth S. Feliberti, Eric C. Perry, Roger R. A Rare Adrenal Incidentaloma That Mimics Adrenocortical Carcinoma |
title | A Rare Adrenal Incidentaloma That Mimics Adrenocortical Carcinoma |
title_full | A Rare Adrenal Incidentaloma That Mimics Adrenocortical Carcinoma |
title_fullStr | A Rare Adrenal Incidentaloma That Mimics Adrenocortical Carcinoma |
title_full_unstemmed | A Rare Adrenal Incidentaloma That Mimics Adrenocortical Carcinoma |
title_short | A Rare Adrenal Incidentaloma That Mimics Adrenocortical Carcinoma |
title_sort | rare adrenal incidentaloma that mimics adrenocortical carcinoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6011133/ https://www.ncbi.nlm.nih.gov/pubmed/29984033 http://dx.doi.org/10.1155/2018/9607972 |
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