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Hemangiolymphangioma of buccal mucosa: A rare case report

Vascular anomalies are mainly classified under two headings, i.e. under vascular tumors and vascular malformations. Hemangioma and lymphangioma are examples for such a vascular anomalies. Malformations may be seen in different combinations of vascular elements, and histologically these vessels may b...

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Autores principales: Manickam, Selvamani, Sasikumar, Prem, Kishore, B Nanda, Joy, Sheethal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596682/
https://www.ncbi.nlm.nih.gov/pubmed/28932041
http://dx.doi.org/10.4103/jomfp.JOMFP_28_17
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author Manickam, Selvamani
Sasikumar, Prem
Kishore, B Nanda
Joy, Sheethal
author_facet Manickam, Selvamani
Sasikumar, Prem
Kishore, B Nanda
Joy, Sheethal
author_sort Manickam, Selvamani
collection PubMed
description Vascular anomalies are mainly classified under two headings, i.e. under vascular tumors and vascular malformations. Hemangioma and lymphangioma are examples for such a vascular anomalies. Malformations may be seen in different combinations of vascular elements, and histologically these vessels may be filled with blood and named lymphangiohemangioma or hemangiolymphangioma according to the dominant tissue structure present. It is a rare developmental anomaly. This paper reports a case of lymphangiohemangioma in a 21-year-old female patient.
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spelling pubmed-55966822017-09-20 Hemangiolymphangioma of buccal mucosa: A rare case report Manickam, Selvamani Sasikumar, Prem Kishore, B Nanda Joy, Sheethal J Oral Maxillofac Pathol Case Report Vascular anomalies are mainly classified under two headings, i.e. under vascular tumors and vascular malformations. Hemangioma and lymphangioma are examples for such a vascular anomalies. Malformations may be seen in different combinations of vascular elements, and histologically these vessels may be filled with blood and named lymphangiohemangioma or hemangiolymphangioma according to the dominant tissue structure present. It is a rare developmental anomaly. This paper reports a case of lymphangiohemangioma in a 21-year-old female patient. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5596682/ /pubmed/28932041 http://dx.doi.org/10.4103/jomfp.JOMFP_28_17 Text en Copyright: © 2017 Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Manickam, Selvamani
Sasikumar, Prem
Kishore, B Nanda
Joy, Sheethal
Hemangiolymphangioma of buccal mucosa: A rare case report
title Hemangiolymphangioma of buccal mucosa: A rare case report
title_full Hemangiolymphangioma of buccal mucosa: A rare case report
title_fullStr Hemangiolymphangioma of buccal mucosa: A rare case report
title_full_unstemmed Hemangiolymphangioma of buccal mucosa: A rare case report
title_short Hemangiolymphangioma of buccal mucosa: A rare case report
title_sort hemangiolymphangioma of buccal mucosa: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596682/
https://www.ncbi.nlm.nih.gov/pubmed/28932041
http://dx.doi.org/10.4103/jomfp.JOMFP_28_17
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