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Cavernous Lymphangioma Arising in the Chest Wall 19 Years after Excision of a Cystic Hygroma

Lymphangioma is a congenital malformation of the lymphatic system and is thought to result from the failure of the lymphatic system to connect with the venous system. Lymphangioma of the chest wall is a very rare disease entity, and only a few cases have ever been documented in the literature. To th...

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Autores principales: Lee, Woo Surng, Kim, Yo Han, Chee, Hyun Keun, Lee, Song Am, Kim, Jong Duk, Kim, Dong Chan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Thoracic and Cardiovascular Surgery 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249346/
https://www.ncbi.nlm.nih.gov/pubmed/22263194
http://dx.doi.org/10.5090/kjtcs.2011.44.5.380
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author Lee, Woo Surng
Kim, Yo Han
Chee, Hyun Keun
Lee, Song Am
Kim, Jong Duk
Kim, Dong Chan
author_facet Lee, Woo Surng
Kim, Yo Han
Chee, Hyun Keun
Lee, Song Am
Kim, Jong Duk
Kim, Dong Chan
author_sort Lee, Woo Surng
collection PubMed
description Lymphangioma is a congenital malformation of the lymphatic system and is thought to result from the failure of the lymphatic system to connect with the venous system. Lymphangioma of the chest wall is a very rare disease entity, and only a few cases have ever been documented in the literature. To the best of our knowledge, there have been few cases of recurrent cavernous lymphangioma after surgical excision of a cystic hygroma on the same side of the chest wall. Here, we report a case of a cavernous lymphangioma of the chest wall in a patient who had undergone surgical excision of a cystic hygroma 19 years earlier.
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spelling pubmed-32493462012-01-19 Cavernous Lymphangioma Arising in the Chest Wall 19 Years after Excision of a Cystic Hygroma Lee, Woo Surng Kim, Yo Han Chee, Hyun Keun Lee, Song Am Kim, Jong Duk Kim, Dong Chan Korean J Thorac Cardiovasc Surg Case Report Lymphangioma is a congenital malformation of the lymphatic system and is thought to result from the failure of the lymphatic system to connect with the venous system. Lymphangioma of the chest wall is a very rare disease entity, and only a few cases have ever been documented in the literature. To the best of our knowledge, there have been few cases of recurrent cavernous lymphangioma after surgical excision of a cystic hygroma on the same side of the chest wall. Here, we report a case of a cavernous lymphangioma of the chest wall in a patient who had undergone surgical excision of a cystic hygroma 19 years earlier. Korean Society for Thoracic and Cardiovascular Surgery 2011-10 2011-10-06 /pmc/articles/PMC3249346/ /pubmed/22263194 http://dx.doi.org/10.5090/kjtcs.2011.44.5.380 Text en © The Korean Society for Thoracic and Cardiovascular Surgery. 2011. All right reserved. This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Lee, Woo Surng
Kim, Yo Han
Chee, Hyun Keun
Lee, Song Am
Kim, Jong Duk
Kim, Dong Chan
Cavernous Lymphangioma Arising in the Chest Wall 19 Years after Excision of a Cystic Hygroma
title Cavernous Lymphangioma Arising in the Chest Wall 19 Years after Excision of a Cystic Hygroma
title_full Cavernous Lymphangioma Arising in the Chest Wall 19 Years after Excision of a Cystic Hygroma
title_fullStr Cavernous Lymphangioma Arising in the Chest Wall 19 Years after Excision of a Cystic Hygroma
title_full_unstemmed Cavernous Lymphangioma Arising in the Chest Wall 19 Years after Excision of a Cystic Hygroma
title_short Cavernous Lymphangioma Arising in the Chest Wall 19 Years after Excision of a Cystic Hygroma
title_sort cavernous lymphangioma arising in the chest wall 19 years after excision of a cystic hygroma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249346/
https://www.ncbi.nlm.nih.gov/pubmed/22263194
http://dx.doi.org/10.5090/kjtcs.2011.44.5.380
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