A supraclavicular cystic lymphangioma in adult: a rare entity

Cystic lymphangioma is a benign congenital disease that is more seen in head and neck regions. We report a case of a 54-year-old man with a growing supraclavicular mass. The ultrasonography and magnetic resonance imaging suggested a cystic lymphangioma. The mass was surgically totally removed withou...

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Autores principales: Rasmont, Céline, Deleuze, Catherine, Ivanov, Todor, Ferdin, Fabian, Lemaitre, Jean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968314/
https://www.ncbi.nlm.nih.gov/pubmed/35368377
http://dx.doi.org/10.1093/jscr/rjac141
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author Rasmont, Céline
Deleuze, Catherine
Ivanov, Todor
Ferdin, Fabian
Lemaitre, Jean
author_facet Rasmont, Céline
Deleuze, Catherine
Ivanov, Todor
Ferdin, Fabian
Lemaitre, Jean
author_sort Rasmont, Céline
collection PubMed
description Cystic lymphangioma is a benign congenital disease that is more seen in head and neck regions. We report a case of a 54-year-old man with a growing supraclavicular mass. The ultrasonography and magnetic resonance imaging suggested a cystic lymphangioma. The mass was surgically totally removed without any recurrence. Histology examination confirmed the diagnosis. Cystic lymphangioma in adults is a rare entity and the literature on the subject is poor with no global recommendations.
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spelling pubmed-89683142022-03-31 A supraclavicular cystic lymphangioma in adult: a rare entity Rasmont, Céline Deleuze, Catherine Ivanov, Todor Ferdin, Fabian Lemaitre, Jean J Surg Case Rep Case Report Cystic lymphangioma is a benign congenital disease that is more seen in head and neck regions. We report a case of a 54-year-old man with a growing supraclavicular mass. The ultrasonography and magnetic resonance imaging suggested a cystic lymphangioma. The mass was surgically totally removed without any recurrence. Histology examination confirmed the diagnosis. Cystic lymphangioma in adults is a rare entity and the literature on the subject is poor with no global recommendations. Oxford University Press 2022-03-30 /pmc/articles/PMC8968314/ /pubmed/35368377 http://dx.doi.org/10.1093/jscr/rjac141 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2022. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Rasmont, Céline
Deleuze, Catherine
Ivanov, Todor
Ferdin, Fabian
Lemaitre, Jean
A supraclavicular cystic lymphangioma in adult: a rare entity
title A supraclavicular cystic lymphangioma in adult: a rare entity
title_full A supraclavicular cystic lymphangioma in adult: a rare entity
title_fullStr A supraclavicular cystic lymphangioma in adult: a rare entity
title_full_unstemmed A supraclavicular cystic lymphangioma in adult: a rare entity
title_short A supraclavicular cystic lymphangioma in adult: a rare entity
title_sort supraclavicular cystic lymphangioma in adult: a rare entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968314/
https://www.ncbi.nlm.nih.gov/pubmed/35368377
http://dx.doi.org/10.1093/jscr/rjac141
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