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Intramuscular Hemangioma of Thyrohyoid Muscle
Intramuscular hemangiomas are rare benign vascular neoplasms. IMH accounts for less than 1% of all hemangiomas. These neoplasms commonly occur in trunk and extremities but are rare in head and neck region. The present case is a 17-year-old female patient, who presented with a painless, slowly enlarg...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018340/ https://www.ncbi.nlm.nih.gov/pubmed/27648331 http://dx.doi.org/10.1155/2016/7158691 |
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author | Parajuli, Ramesh Thapa, Suman Maharjan, Sushna |
author_facet | Parajuli, Ramesh Thapa, Suman Maharjan, Sushna |
author_sort | Parajuli, Ramesh |
collection | PubMed |
description | Intramuscular hemangiomas are rare benign vascular neoplasms. IMH accounts for less than 1% of all hemangiomas. These neoplasms commonly occur in trunk and extremities but are rare in head and neck region. The present case is a 17-year-old female patient, who presented with a painless, slowly enlarging mass in left sided upper neck for 4 years. Investigations were suggestive of vascular neoplasm. She underwent excision of the mass in toto under general anesthesia. Postoperative period was uneventful. Histopathological examination of the mass revealed it as mixed type of intramuscular hemangioma. She did not have any signs of recurrences on her last follow-up at 6 months postoperatively. This case report discusses the rare IMH arising from thyrohyoid strap muscle. |
format | Online Article Text |
id | pubmed-5018340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-50183402016-09-19 Intramuscular Hemangioma of Thyrohyoid Muscle Parajuli, Ramesh Thapa, Suman Maharjan, Sushna Case Rep Otolaryngol Case Report Intramuscular hemangiomas are rare benign vascular neoplasms. IMH accounts for less than 1% of all hemangiomas. These neoplasms commonly occur in trunk and extremities but are rare in head and neck region. The present case is a 17-year-old female patient, who presented with a painless, slowly enlarging mass in left sided upper neck for 4 years. Investigations were suggestive of vascular neoplasm. She underwent excision of the mass in toto under general anesthesia. Postoperative period was uneventful. Histopathological examination of the mass revealed it as mixed type of intramuscular hemangioma. She did not have any signs of recurrences on her last follow-up at 6 months postoperatively. This case report discusses the rare IMH arising from thyrohyoid strap muscle. Hindawi Publishing Corporation 2016 2016-08-28 /pmc/articles/PMC5018340/ /pubmed/27648331 http://dx.doi.org/10.1155/2016/7158691 Text en Copyright © 2016 Ramesh Parajuli et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Parajuli, Ramesh Thapa, Suman Maharjan, Sushna Intramuscular Hemangioma of Thyrohyoid Muscle |
title | Intramuscular Hemangioma of Thyrohyoid Muscle |
title_full | Intramuscular Hemangioma of Thyrohyoid Muscle |
title_fullStr | Intramuscular Hemangioma of Thyrohyoid Muscle |
title_full_unstemmed | Intramuscular Hemangioma of Thyrohyoid Muscle |
title_short | Intramuscular Hemangioma of Thyrohyoid Muscle |
title_sort | intramuscular hemangioma of thyrohyoid muscle |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018340/ https://www.ncbi.nlm.nih.gov/pubmed/27648331 http://dx.doi.org/10.1155/2016/7158691 |
work_keys_str_mv | AT parajuliramesh intramuscularhemangiomaofthyrohyoidmuscle AT thapasuman intramuscularhemangiomaofthyrohyoidmuscle AT maharjansushna intramuscularhemangiomaofthyrohyoidmuscle |