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Case Report: Challenging Otologic Surgery in Patients With 22q11.2 Deletion Syndrome
Patients with 22q11.2 deletion syndrome frequently have conductive hearing loss and/or chronic otitis media. Otologic surgery is often opted for. We present two patients undergoing otologic surgery. This case report outlines the typical otologic surgical challenges in patients with 22q11.2 deletion...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7461837/ https://www.ncbi.nlm.nih.gov/pubmed/32974381 http://dx.doi.org/10.3389/fsurg.2020.00053 |
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author | Verheij, Emmy Markodimitraki, Laura M. Stokroos, Robert J. Thomeer, Hans G. X. M. |
author_facet | Verheij, Emmy Markodimitraki, Laura M. Stokroos, Robert J. Thomeer, Hans G. X. M. |
author_sort | Verheij, Emmy |
collection | PubMed |
description | Patients with 22q11.2 deletion syndrome frequently have conductive hearing loss and/or chronic otitis media. Otologic surgery is often opted for. We present two patients undergoing otologic surgery. This case report outlines the typical otologic surgical challenges in patients with 22q11.2 deletion syndrome. Case one is a 52 year old male patient with chronic otitis media who underwent a mastoidectomy. The pre-operative CT scan showed a fused lateral semicircular canal and vestibule. Peroperatively, the lateral semicircular canal could not be used as a landmark to identify the facial nerve. Case two is a 10 year old female patient with conductive hearing loss. A middle ear inspection was performed where a bony epitympanic fixation of the malleus was encountered. In addition, the manubrium of the malleus was atrophic and also fixated. The bony fixation was removed, as was the manubrium of the malleus. Otologists should be aware of these typical anatomical variations in patients with 22q11.2 deletion syndrome. We recommend to use CT scanning of the middle and inner ear when preparing for otologic surgery in 22q11.2 deletion syndrome. |
format | Online Article Text |
id | pubmed-7461837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74618372020-09-23 Case Report: Challenging Otologic Surgery in Patients With 22q11.2 Deletion Syndrome Verheij, Emmy Markodimitraki, Laura M. Stokroos, Robert J. Thomeer, Hans G. X. M. Front Surg Surgery Patients with 22q11.2 deletion syndrome frequently have conductive hearing loss and/or chronic otitis media. Otologic surgery is often opted for. We present two patients undergoing otologic surgery. This case report outlines the typical otologic surgical challenges in patients with 22q11.2 deletion syndrome. Case one is a 52 year old male patient with chronic otitis media who underwent a mastoidectomy. The pre-operative CT scan showed a fused lateral semicircular canal and vestibule. Peroperatively, the lateral semicircular canal could not be used as a landmark to identify the facial nerve. Case two is a 10 year old female patient with conductive hearing loss. A middle ear inspection was performed where a bony epitympanic fixation of the malleus was encountered. In addition, the manubrium of the malleus was atrophic and also fixated. The bony fixation was removed, as was the manubrium of the malleus. Otologists should be aware of these typical anatomical variations in patients with 22q11.2 deletion syndrome. We recommend to use CT scanning of the middle and inner ear when preparing for otologic surgery in 22q11.2 deletion syndrome. Frontiers Media S.A. 2020-08-18 /pmc/articles/PMC7461837/ /pubmed/32974381 http://dx.doi.org/10.3389/fsurg.2020.00053 Text en Copyright © 2020 Verheij, Markodimitraki, Stokroos and Thomeer. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Surgery Verheij, Emmy Markodimitraki, Laura M. Stokroos, Robert J. Thomeer, Hans G. X. M. Case Report: Challenging Otologic Surgery in Patients With 22q11.2 Deletion Syndrome |
title | Case Report: Challenging Otologic Surgery in Patients With 22q11.2 Deletion Syndrome |
title_full | Case Report: Challenging Otologic Surgery in Patients With 22q11.2 Deletion Syndrome |
title_fullStr | Case Report: Challenging Otologic Surgery in Patients With 22q11.2 Deletion Syndrome |
title_full_unstemmed | Case Report: Challenging Otologic Surgery in Patients With 22q11.2 Deletion Syndrome |
title_short | Case Report: Challenging Otologic Surgery in Patients With 22q11.2 Deletion Syndrome |
title_sort | case report: challenging otologic surgery in patients with 22q11.2 deletion syndrome |
topic | Surgery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7461837/ https://www.ncbi.nlm.nih.gov/pubmed/32974381 http://dx.doi.org/10.3389/fsurg.2020.00053 |
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