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Case report: Heterotopic intrarenally located adrenocortical oncocytoma

The clinical case of a 65-year-old woman with an incidentally detected left-sided mass in the upper renal pole is presented. A functional adrenal tumor was excluded. The mass was removed retroperitoneoscopically. The perioperative period was uneventful. The histopathological examination revealed a h...

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Autores principales: Godin, Konstantin, Bang, Nicole, Tolkach, Yuri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168838/
https://www.ncbi.nlm.nih.gov/pubmed/25254096
http://dx.doi.org/10.12688/f1000research.3780.1
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author Godin, Konstantin
Bang, Nicole
Tolkach, Yuri
author_facet Godin, Konstantin
Bang, Nicole
Tolkach, Yuri
author_sort Godin, Konstantin
collection PubMed
description The clinical case of a 65-year-old woman with an incidentally detected left-sided mass in the upper renal pole is presented. A functional adrenal tumor was excluded. The mass was removed retroperitoneoscopically. The perioperative period was uneventful. The histopathological examination revealed a heterotopic intrarenal adrenocortical oncocytoma. Adrenal oncocytic neoplasms are very rare, with, to the authors’ knowledge, only 159 described cases so far. Most cases are non-functioning adenomas that can reach a considerable size. Only 10 heterotopic adrenal oncocytomas have been described (three retroperitoneal and seven intraspinal cases). Although the intrarenal adrenal rest is the most frequently appearing variant of adrenal heterotopia, to the best of our knowledge, this report is the first description of an intrarenally growing adrenocortical oncocytic adenoma. In addition to retroperitoneally located oncocytomas, this case could be interesting for urological practice because there are no diagnostic features which could provide a secure preoperative diagnosis of an adrenal oncocytic neoplasm and its malignant variant. Generally accepted indications for surgery of adrenal masses have to be respected. The definitive pathologic diagnosis is in most cases surprising because of its rarity. Benign adrenal oncocytic neoplasms do not require any adjuvant treatment. The oncocytic variant of adrenocortical carcinoma generally has a poor prognosis.
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spelling pubmed-41688382014-09-23 Case report: Heterotopic intrarenally located adrenocortical oncocytoma Godin, Konstantin Bang, Nicole Tolkach, Yuri F1000Res Case Report The clinical case of a 65-year-old woman with an incidentally detected left-sided mass in the upper renal pole is presented. A functional adrenal tumor was excluded. The mass was removed retroperitoneoscopically. The perioperative period was uneventful. The histopathological examination revealed a heterotopic intrarenal adrenocortical oncocytoma. Adrenal oncocytic neoplasms are very rare, with, to the authors’ knowledge, only 159 described cases so far. Most cases are non-functioning adenomas that can reach a considerable size. Only 10 heterotopic adrenal oncocytomas have been described (three retroperitoneal and seven intraspinal cases). Although the intrarenal adrenal rest is the most frequently appearing variant of adrenal heterotopia, to the best of our knowledge, this report is the first description of an intrarenally growing adrenocortical oncocytic adenoma. In addition to retroperitoneally located oncocytomas, this case could be interesting for urological practice because there are no diagnostic features which could provide a secure preoperative diagnosis of an adrenal oncocytic neoplasm and its malignant variant. Generally accepted indications for surgery of adrenal masses have to be respected. The definitive pathologic diagnosis is in most cases surprising because of its rarity. Benign adrenal oncocytic neoplasms do not require any adjuvant treatment. The oncocytic variant of adrenocortical carcinoma generally has a poor prognosis. F1000Research 2014-03-17 /pmc/articles/PMC4168838/ /pubmed/25254096 http://dx.doi.org/10.12688/f1000research.3780.1 Text en Copyright: © 2014 Godin K et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/publicdomain/zero/1.0/ Data associated with the article are available under the terms of the Creative Commons Zero "No rights reserved" data waiver (CC0 1.0 Public domain dedication).
spellingShingle Case Report
Godin, Konstantin
Bang, Nicole
Tolkach, Yuri
Case report: Heterotopic intrarenally located adrenocortical oncocytoma
title Case report: Heterotopic intrarenally located adrenocortical oncocytoma
title_full Case report: Heterotopic intrarenally located adrenocortical oncocytoma
title_fullStr Case report: Heterotopic intrarenally located adrenocortical oncocytoma
title_full_unstemmed Case report: Heterotopic intrarenally located adrenocortical oncocytoma
title_short Case report: Heterotopic intrarenally located adrenocortical oncocytoma
title_sort case report: heterotopic intrarenally located adrenocortical oncocytoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168838/
https://www.ncbi.nlm.nih.gov/pubmed/25254096
http://dx.doi.org/10.12688/f1000research.3780.1
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