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A Rare Case of an Adrenal Mass Proved to Be a Benign Cellular Schwannoma

Adrenal schwannomas are extremely uncommon tumors. We report the case of a 39-year-old male with a right adrenal mass. Laboratory tests were normal and radiological exams revealed the adrenal tumor. Open surgical adrenalectomy was performed. The postoperative course was uneventful. Microscopy and im...

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Detalles Bibliográficos
Autores principales: Galanis, Ilias, Floros, Georgios
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9013506/
https://www.ncbi.nlm.nih.gov/pubmed/35464584
http://dx.doi.org/10.7759/cureus.23296
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author Galanis, Ilias
Floros, Georgios
author_facet Galanis, Ilias
Floros, Georgios
author_sort Galanis, Ilias
collection PubMed
description Adrenal schwannomas are extremely uncommon tumors. We report the case of a 39-year-old male with a right adrenal mass. Laboratory tests were normal and radiological exams revealed the adrenal tumor. Open surgical adrenalectomy was performed. The postoperative course was uneventful. Microscopy and immunohistochemistry revealed a cellular schwannoma. Adrenal schwannomas are rare tumors, very difficult to diagnose in preoperative evaluation. Surgical excision of the tumor, histological and immunohistochemical examination of the specimen provide a definitive diagnosis. Prognosis is generally very good. Recurrence rates are related to positive surgical margins.
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spelling pubmed-90135062022-04-22 A Rare Case of an Adrenal Mass Proved to Be a Benign Cellular Schwannoma Galanis, Ilias Floros, Georgios Cureus Endocrinology/Diabetes/Metabolism Adrenal schwannomas are extremely uncommon tumors. We report the case of a 39-year-old male with a right adrenal mass. Laboratory tests were normal and radiological exams revealed the adrenal tumor. Open surgical adrenalectomy was performed. The postoperative course was uneventful. Microscopy and immunohistochemistry revealed a cellular schwannoma. Adrenal schwannomas are rare tumors, very difficult to diagnose in preoperative evaluation. Surgical excision of the tumor, histological and immunohistochemical examination of the specimen provide a definitive diagnosis. Prognosis is generally very good. Recurrence rates are related to positive surgical margins. Cureus 2022-03-18 /pmc/articles/PMC9013506/ /pubmed/35464584 http://dx.doi.org/10.7759/cureus.23296 Text en Copyright © 2022, Galanis et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Endocrinology/Diabetes/Metabolism
Galanis, Ilias
Floros, Georgios
A Rare Case of an Adrenal Mass Proved to Be a Benign Cellular Schwannoma
title A Rare Case of an Adrenal Mass Proved to Be a Benign Cellular Schwannoma
title_full A Rare Case of an Adrenal Mass Proved to Be a Benign Cellular Schwannoma
title_fullStr A Rare Case of an Adrenal Mass Proved to Be a Benign Cellular Schwannoma
title_full_unstemmed A Rare Case of an Adrenal Mass Proved to Be a Benign Cellular Schwannoma
title_short A Rare Case of an Adrenal Mass Proved to Be a Benign Cellular Schwannoma
title_sort rare case of an adrenal mass proved to be a benign cellular schwannoma
topic Endocrinology/Diabetes/Metabolism
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9013506/
https://www.ncbi.nlm.nih.gov/pubmed/35464584
http://dx.doi.org/10.7759/cureus.23296
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