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An extremely rare pedunculated lipoma of the hypopharynx: A case report
BACKGROUND: Hypopharyngeal lipoma is a rare disease that can lead to asphyxiation after aspiration. Sclerotic lipoma in the hypopharynx is an extremely rare histological type. Hypopharyngeal lipoma should be resected in time after diagnosis. CASE SUMMARY: An 86-year-old female patient presented to o...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745315/ https://www.ncbi.nlm.nih.gov/pubmed/31559306 http://dx.doi.org/10.12998/wjcc.v7.i17.2652 |
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author | Sun, Qiang Zhang, Chun-Lin Liu, Zhao-Hui |
author_facet | Sun, Qiang Zhang, Chun-Lin Liu, Zhao-Hui |
author_sort | Sun, Qiang |
collection | PubMed |
description | BACKGROUND: Hypopharyngeal lipoma is a rare disease that can lead to asphyxiation after aspiration. Sclerotic lipoma in the hypopharynx is an extremely rare histological type. Hypopharyngeal lipoma should be resected in time after diagnosis. CASE SUMMARY: An 86-year-old female patient presented to our department with a long pedunculated mass protruding from her mouth. Until this time, the patient had no dyspnea, dysphagia, or throat discomfort. Physical examination showed stable vital signs and clear consciousness. The pedicel was derived from the posterior wall of the hypopharynx. The tumor was smooth, hyperemic and dark red, about 10 cm long, and 4 cm wide. In order to prevent airway obstruction, the hypopharyngeal tumor was excised in emergent operation. The pharyngeal cavity was exposed by a mouth gag during the operation. A disposable plasma knife was used to completely remove the tumor along the base of the new organism, and no active bleeding occurred. The postoperative pathological results were sclerotic lipoma. CONCLUSION: Lipoma in the pharynx is relatively rare. Patients with this condition must be referred immediately to Ear-Nose-Throat specialists and complete surgical excision should be performed as soon as possible to prevent serious complications, such as airway obstruction and death. |
format | Online Article Text |
id | pubmed-6745315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-67453152019-09-26 An extremely rare pedunculated lipoma of the hypopharynx: A case report Sun, Qiang Zhang, Chun-Lin Liu, Zhao-Hui World J Clin Cases Case Report BACKGROUND: Hypopharyngeal lipoma is a rare disease that can lead to asphyxiation after aspiration. Sclerotic lipoma in the hypopharynx is an extremely rare histological type. Hypopharyngeal lipoma should be resected in time after diagnosis. CASE SUMMARY: An 86-year-old female patient presented to our department with a long pedunculated mass protruding from her mouth. Until this time, the patient had no dyspnea, dysphagia, or throat discomfort. Physical examination showed stable vital signs and clear consciousness. The pedicel was derived from the posterior wall of the hypopharynx. The tumor was smooth, hyperemic and dark red, about 10 cm long, and 4 cm wide. In order to prevent airway obstruction, the hypopharyngeal tumor was excised in emergent operation. The pharyngeal cavity was exposed by a mouth gag during the operation. A disposable plasma knife was used to completely remove the tumor along the base of the new organism, and no active bleeding occurred. The postoperative pathological results were sclerotic lipoma. CONCLUSION: Lipoma in the pharynx is relatively rare. Patients with this condition must be referred immediately to Ear-Nose-Throat specialists and complete surgical excision should be performed as soon as possible to prevent serious complications, such as airway obstruction and death. Baishideng Publishing Group Inc 2019-09-06 2019-09-06 /pmc/articles/PMC6745315/ /pubmed/31559306 http://dx.doi.org/10.12998/wjcc.v7.i17.2652 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Case Report Sun, Qiang Zhang, Chun-Lin Liu, Zhao-Hui An extremely rare pedunculated lipoma of the hypopharynx: A case report |
title | An extremely rare pedunculated lipoma of the hypopharynx: A case report |
title_full | An extremely rare pedunculated lipoma of the hypopharynx: A case report |
title_fullStr | An extremely rare pedunculated lipoma of the hypopharynx: A case report |
title_full_unstemmed | An extremely rare pedunculated lipoma of the hypopharynx: A case report |
title_short | An extremely rare pedunculated lipoma of the hypopharynx: A case report |
title_sort | extremely rare pedunculated lipoma of the hypopharynx: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745315/ https://www.ncbi.nlm.nih.gov/pubmed/31559306 http://dx.doi.org/10.12998/wjcc.v7.i17.2652 |
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