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Ossicular osteoma of the malleus—A rare diagnosis of middle ear mass
Osteoma of the middle ear (MEO) is a rarity. Due to the benign nature and slow growth rate, MEO are often occasionally found by chance. Possible unspecific clinical symptoms may be conductive hearing loss, tinnitus, effusion, and a sense of fullness. If the osteoma is small and not visible in the ot...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520498/ https://www.ncbi.nlm.nih.gov/pubmed/36188094 http://dx.doi.org/10.1016/j.radcr.2022.08.083 |
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author | Sievert, Matti Mantsopoulos, Konstantinos Hornung, Joachim Thimsen, Vivian Heiss, Rafael Kopp, Markus Wetzl, Matthias Iro, Heinrich Uder, Michael Wiesmueller, Marco |
author_facet | Sievert, Matti Mantsopoulos, Konstantinos Hornung, Joachim Thimsen, Vivian Heiss, Rafael Kopp, Markus Wetzl, Matthias Iro, Heinrich Uder, Michael Wiesmueller, Marco |
author_sort | Sievert, Matti |
collection | PubMed |
description | Osteoma of the middle ear (MEO) is a rarity. Due to the benign nature and slow growth rate, MEO are often occasionally found by chance. Possible unspecific clinical symptoms may be conductive hearing loss, tinnitus, effusion, and a sense of fullness. If the osteoma is small and not visible in the otoscopic inspection, it may be confused with other conductive hearing loss etiologies, such as otosclerosis. Nevertheless, one should be aware of this rare but important differential diagnosis of middle ear lesions. This article presents an MEO case causing conductive hearing loss and outlines the diagnostic approach with computed tomography. |
format | Online Article Text |
id | pubmed-9520498 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-95204982022-09-30 Ossicular osteoma of the malleus—A rare diagnosis of middle ear mass Sievert, Matti Mantsopoulos, Konstantinos Hornung, Joachim Thimsen, Vivian Heiss, Rafael Kopp, Markus Wetzl, Matthias Iro, Heinrich Uder, Michael Wiesmueller, Marco Radiol Case Rep Case Report Osteoma of the middle ear (MEO) is a rarity. Due to the benign nature and slow growth rate, MEO are often occasionally found by chance. Possible unspecific clinical symptoms may be conductive hearing loss, tinnitus, effusion, and a sense of fullness. If the osteoma is small and not visible in the otoscopic inspection, it may be confused with other conductive hearing loss etiologies, such as otosclerosis. Nevertheless, one should be aware of this rare but important differential diagnosis of middle ear lesions. This article presents an MEO case causing conductive hearing loss and outlines the diagnostic approach with computed tomography. Elsevier 2022-09-16 /pmc/articles/PMC9520498/ /pubmed/36188094 http://dx.doi.org/10.1016/j.radcr.2022.08.083 Text en © 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Sievert, Matti Mantsopoulos, Konstantinos Hornung, Joachim Thimsen, Vivian Heiss, Rafael Kopp, Markus Wetzl, Matthias Iro, Heinrich Uder, Michael Wiesmueller, Marco Ossicular osteoma of the malleus—A rare diagnosis of middle ear mass |
title | Ossicular osteoma of the malleus—A rare diagnosis of middle ear mass |
title_full | Ossicular osteoma of the malleus—A rare diagnosis of middle ear mass |
title_fullStr | Ossicular osteoma of the malleus—A rare diagnosis of middle ear mass |
title_full_unstemmed | Ossicular osteoma of the malleus—A rare diagnosis of middle ear mass |
title_short | Ossicular osteoma of the malleus—A rare diagnosis of middle ear mass |
title_sort | ossicular osteoma of the malleus—a rare diagnosis of middle ear mass |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520498/ https://www.ncbi.nlm.nih.gov/pubmed/36188094 http://dx.doi.org/10.1016/j.radcr.2022.08.083 |
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