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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...

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Detalles Bibliográficos
Autores principales: Parajuli, Ramesh, Thapa, Suman, Maharjan, Sushna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
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.
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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
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