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Neuroglial Choristoma of the Middle Ear with Massive Tympanosclerosis: A Case Report and Literature Review

Neuroglialchoristoma is a rare cerebral heterotopia typically involving extracranial midline structures of the head and neck, including the nose, nasopharynx and oral cavity. It rarely involves non-midline structures, such as the middle ear, mastoid and orbit. We report the case of a 63-year-old wom...

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Autores principales: Shim, Hyun Joon, Kang, Yong Kyung, An, Yong-Hwi, Hong, Young Ok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Audiological Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5144819/
https://www.ncbi.nlm.nih.gov/pubmed/27942605
http://dx.doi.org/10.7874/jao.2016.20.3.179
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author Shim, Hyun Joon
Kang, Yong Kyung
An, Yong-Hwi
Hong, Young Ok
author_facet Shim, Hyun Joon
Kang, Yong Kyung
An, Yong-Hwi
Hong, Young Ok
author_sort Shim, Hyun Joon
collection PubMed
description Neuroglialchoristoma is a rare cerebral heterotopia typically involving extracranial midline structures of the head and neck, including the nose, nasopharynx and oral cavity. It rarely involves non-midline structures, such as the middle ear, mastoid and orbit. We report the case of a 63-year-old woman with right-sided hearing loss and aural fullness who was diagnosed with neuroglialchoristoma of the middle ear and mastoid. To our knowledge, this is the first report on neuroglialchoristomawith massive tympanosclerosis. The presence of combination supported the inhalation theory of neuroglialchoristoma, given that tympanosclerosis is typically caused by Eustachian tube dysfunction.
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spelling pubmed-51448192016-12-09 Neuroglial Choristoma of the Middle Ear with Massive Tympanosclerosis: A Case Report and Literature Review Shim, Hyun Joon Kang, Yong Kyung An, Yong-Hwi Hong, Young Ok J Audiol Otol Case Report Neuroglialchoristoma is a rare cerebral heterotopia typically involving extracranial midline structures of the head and neck, including the nose, nasopharynx and oral cavity. It rarely involves non-midline structures, such as the middle ear, mastoid and orbit. We report the case of a 63-year-old woman with right-sided hearing loss and aural fullness who was diagnosed with neuroglialchoristoma of the middle ear and mastoid. To our knowledge, this is the first report on neuroglialchoristomawith massive tympanosclerosis. The presence of combination supported the inhalation theory of neuroglialchoristoma, given that tympanosclerosis is typically caused by Eustachian tube dysfunction. The Korean Audiological Society 2016-12 2016-11-30 /pmc/articles/PMC5144819/ /pubmed/27942605 http://dx.doi.org/10.7874/jao.2016.20.3.179 Text en Copyright © 2016 The Korean Audiological Society http://creativecommons.org/licenses/by-nc/3.0/ 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
Shim, Hyun Joon
Kang, Yong Kyung
An, Yong-Hwi
Hong, Young Ok
Neuroglial Choristoma of the Middle Ear with Massive Tympanosclerosis: A Case Report and Literature Review
title Neuroglial Choristoma of the Middle Ear with Massive Tympanosclerosis: A Case Report and Literature Review
title_full Neuroglial Choristoma of the Middle Ear with Massive Tympanosclerosis: A Case Report and Literature Review
title_fullStr Neuroglial Choristoma of the Middle Ear with Massive Tympanosclerosis: A Case Report and Literature Review
title_full_unstemmed Neuroglial Choristoma of the Middle Ear with Massive Tympanosclerosis: A Case Report and Literature Review
title_short Neuroglial Choristoma of the Middle Ear with Massive Tympanosclerosis: A Case Report and Literature Review
title_sort neuroglial choristoma of the middle ear with massive tympanosclerosis: a case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5144819/
https://www.ncbi.nlm.nih.gov/pubmed/27942605
http://dx.doi.org/10.7874/jao.2016.20.3.179
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