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Adrenal cavernous Hemangioma;A rare diagnosis of adrenal incidentaloma:A case report, and literature review

Adrenal cavernous hemangioma is an extremely rare benign tumor. To date, less than 70 cases have been reported in the literature. In most of the cases, the tumor is hormonally silent, discovered incidentally and the diagnosis is made postoperatively. Pre-operative differentiation between this benign...

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Autores principales: Al-Rawashdah, Samer, Mansi, Hammam, Pastore, Antonio Luigi, Carbone, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653277/
https://www.ncbi.nlm.nih.gov/pubmed/33204642
http://dx.doi.org/10.1016/j.eucr.2020.101477
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author Al-Rawashdah, Samer
Mansi, Hammam
Pastore, Antonio Luigi
Carbone, Antonio
author_facet Al-Rawashdah, Samer
Mansi, Hammam
Pastore, Antonio Luigi
Carbone, Antonio
author_sort Al-Rawashdah, Samer
collection PubMed
description Adrenal cavernous hemangioma is an extremely rare benign tumor. To date, less than 70 cases have been reported in the literature. In most of the cases, the tumor is hormonally silent, discovered incidentally and the diagnosis is made postoperatively. Pre-operative differentiation between this benign tumor and other malignant adrenal tumors is challenging. In this article we present a case of a non-functioning adrenal incidentaloma that was managed by laparoscopic adrenalectomy. The post-operative histological diagnosis was adrenal cavernous hemangioma.
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spelling pubmed-76532772020-11-16 Adrenal cavernous Hemangioma;A rare diagnosis of adrenal incidentaloma:A case report, and literature review Al-Rawashdah, Samer Mansi, Hammam Pastore, Antonio Luigi Carbone, Antonio Urol Case Rep Oncology Adrenal cavernous hemangioma is an extremely rare benign tumor. To date, less than 70 cases have been reported in the literature. In most of the cases, the tumor is hormonally silent, discovered incidentally and the diagnosis is made postoperatively. Pre-operative differentiation between this benign tumor and other malignant adrenal tumors is challenging. In this article we present a case of a non-functioning adrenal incidentaloma that was managed by laparoscopic adrenalectomy. The post-operative histological diagnosis was adrenal cavernous hemangioma. Elsevier 2020-10-31 /pmc/articles/PMC7653277/ /pubmed/33204642 http://dx.doi.org/10.1016/j.eucr.2020.101477 Text en © 2020 Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Oncology
Al-Rawashdah, Samer
Mansi, Hammam
Pastore, Antonio Luigi
Carbone, Antonio
Adrenal cavernous Hemangioma;A rare diagnosis of adrenal incidentaloma:A case report, and literature review
title Adrenal cavernous Hemangioma;A rare diagnosis of adrenal incidentaloma:A case report, and literature review
title_full Adrenal cavernous Hemangioma;A rare diagnosis of adrenal incidentaloma:A case report, and literature review
title_fullStr Adrenal cavernous Hemangioma;A rare diagnosis of adrenal incidentaloma:A case report, and literature review
title_full_unstemmed Adrenal cavernous Hemangioma;A rare diagnosis of adrenal incidentaloma:A case report, and literature review
title_short Adrenal cavernous Hemangioma;A rare diagnosis of adrenal incidentaloma:A case report, and literature review
title_sort adrenal cavernous hemangioma;a rare diagnosis of adrenal incidentaloma:a case report, and literature review
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653277/
https://www.ncbi.nlm.nih.gov/pubmed/33204642
http://dx.doi.org/10.1016/j.eucr.2020.101477
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