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Lymphangiomatous endothelial cyst of the adrenal gland: A case report

Cystic adrenal tumors are rare with an incidence of approximately 0.06% in the general population. Four main histological types are distinguished: Endothelial cysts of lymphangiomatous or angiomatous origin, pseudocysts, epithelial cysts and cysts of parasitic origin. Surgery is recommended for sign...

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Autores principales: Issam, Rekik, Amine, Mseddi Mohamed, Meriam, Triki, Ahmed, Chaabouni, Mehdi, Bouassida, Mourad, Hadj Slimen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479637/
https://www.ncbi.nlm.nih.gov/pubmed/34621624
http://dx.doi.org/10.1016/j.eucr.2021.101859
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author Issam, Rekik
Amine, Mseddi Mohamed
Meriam, Triki
Ahmed, Chaabouni
Mehdi, Bouassida
Mourad, Hadj Slimen
author_facet Issam, Rekik
Amine, Mseddi Mohamed
Meriam, Triki
Ahmed, Chaabouni
Mehdi, Bouassida
Mourad, Hadj Slimen
author_sort Issam, Rekik
collection PubMed
description Cystic adrenal tumors are rare with an incidence of approximately 0.06% in the general population. Four main histological types are distinguished: Endothelial cysts of lymphangiomatous or angiomatous origin, pseudocysts, epithelial cysts and cysts of parasitic origin. Surgery is recommended for signs of complications, suspicion of malignancy and large size. In other cases, simple surveillance can be proposed. We report here a case of a lymphangiomatous endothelial cyst of the adrenal gland. The objective is to recall the clinical characteristics and to specify the diagnostic contribution of imaging as well as the therapeutic modalities of this entity.
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spelling pubmed-84796372021-10-06 Lymphangiomatous endothelial cyst of the adrenal gland: A case report Issam, Rekik Amine, Mseddi Mohamed Meriam, Triki Ahmed, Chaabouni Mehdi, Bouassida Mourad, Hadj Slimen Urol Case Rep Functional Urology Cystic adrenal tumors are rare with an incidence of approximately 0.06% in the general population. Four main histological types are distinguished: Endothelial cysts of lymphangiomatous or angiomatous origin, pseudocysts, epithelial cysts and cysts of parasitic origin. Surgery is recommended for signs of complications, suspicion of malignancy and large size. In other cases, simple surveillance can be proposed. We report here a case of a lymphangiomatous endothelial cyst of the adrenal gland. The objective is to recall the clinical characteristics and to specify the diagnostic contribution of imaging as well as the therapeutic modalities of this entity. Elsevier 2021-09-18 /pmc/articles/PMC8479637/ /pubmed/34621624 http://dx.doi.org/10.1016/j.eucr.2021.101859 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Functional Urology
Issam, Rekik
Amine, Mseddi Mohamed
Meriam, Triki
Ahmed, Chaabouni
Mehdi, Bouassida
Mourad, Hadj Slimen
Lymphangiomatous endothelial cyst of the adrenal gland: A case report
title Lymphangiomatous endothelial cyst of the adrenal gland: A case report
title_full Lymphangiomatous endothelial cyst of the adrenal gland: A case report
title_fullStr Lymphangiomatous endothelial cyst of the adrenal gland: A case report
title_full_unstemmed Lymphangiomatous endothelial cyst of the adrenal gland: A case report
title_short Lymphangiomatous endothelial cyst of the adrenal gland: A case report
title_sort lymphangiomatous endothelial cyst of the adrenal gland: a case report
topic Functional Urology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479637/
https://www.ncbi.nlm.nih.gov/pubmed/34621624
http://dx.doi.org/10.1016/j.eucr.2021.101859
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