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De novo sensorineural hearing loss sequelae of narrow, duplicated internal auditory canal: Case series and literature review
INTRODUCTION: A narrow duplicated internal auditory canal (IAC) is an extremely rare anomaly, likely associated with congenital sensorineural hearing loss due to aplasia/hypoplasia of the vestibulocochlear nerve or the cochlear branch alone. We aimed to review our experience with IAC duplication, de...
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/PMC9121248/ https://www.ncbi.nlm.nih.gov/pubmed/35594789 http://dx.doi.org/10.1016/j.ijscr.2022.107109 |
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author | AlEnazi, Abdulaziz Saud Alshaiji, Abdulaziz Alenezi, Meaad Al-Sharydah, Abdulaziz Alsuhibani, Sari Alhaidey, Ali Samarah, Adnan AlQahtani, Munahi |
author_facet | AlEnazi, Abdulaziz Saud Alshaiji, Abdulaziz Alenezi, Meaad Al-Sharydah, Abdulaziz Alsuhibani, Sari Alhaidey, Ali Samarah, Adnan AlQahtani, Munahi |
author_sort | AlEnazi, Abdulaziz Saud |
collection | PubMed |
description | INTRODUCTION: A narrow duplicated internal auditory canal (IAC) is an extremely rare anomaly, likely associated with congenital sensorineural hearing loss due to aplasia/hypoplasia of the vestibulocochlear nerve or the cochlear branch alone. We aimed to review our experience with IAC duplication, describe its clinical characteristics, and present a literature review. CASE PRESENTATION: Our Otology database was searched for children who showed duplication of the IAC. Clinical characteristics of two children with bilateral duplication of the IAC are described. Data regarding clinical history, auditory assessment, magnetic resonance imaging (MRI), and computed tomography (CT) were collected and analyzed. The separated, accessory bony canals were demonstrated on high-resolution CT scans, and the nerves were demonstrated on MRI. DISCUSSION: To date, a few cases of narrow duplicate IAC have been reported in the literature, Approximately 20% of patients with congenital SNHL are found to show inner-ear bony abnormalities on CT, but much uncertainty still exists about the mechanism underlying IAC stenosis.(5) Imaging findings of the temporal bone in our case series demonstrated asymmetrical narrowing of both IACs, there is no clear evidence in the literature supporting the predominance of one side over the other. In our series, facial nerve function was intact bilaterally. As for our cases, both patients were enrolled in a single-sided deafness evaluation for a trial of options such as BAHA, CROS, cochlear implants, and other non-implantable hearing aids. Furthermore, addressing the important factors will optimize the outcomes including surgery at early age to optimize neural plasticity, with intense long-term therapy. CONCLUSION: Congenital duplication of the IAC likely convoying sensorineural hearing loss due to aplasia/hypoplasia of the vestibulocochlear nerve. Early diagnosis and intervention are essential to optimize patient outcomes. |
format | Online Article Text |
id | pubmed-9121248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-91212482022-05-21 De novo sensorineural hearing loss sequelae of narrow, duplicated internal auditory canal: Case series and literature review AlEnazi, Abdulaziz Saud Alshaiji, Abdulaziz Alenezi, Meaad Al-Sharydah, Abdulaziz Alsuhibani, Sari Alhaidey, Ali Samarah, Adnan AlQahtani, Munahi Int J Surg Case Rep Case Series INTRODUCTION: A narrow duplicated internal auditory canal (IAC) is an extremely rare anomaly, likely associated with congenital sensorineural hearing loss due to aplasia/hypoplasia of the vestibulocochlear nerve or the cochlear branch alone. We aimed to review our experience with IAC duplication, describe its clinical characteristics, and present a literature review. CASE PRESENTATION: Our Otology database was searched for children who showed duplication of the IAC. Clinical characteristics of two children with bilateral duplication of the IAC are described. Data regarding clinical history, auditory assessment, magnetic resonance imaging (MRI), and computed tomography (CT) were collected and analyzed. The separated, accessory bony canals were demonstrated on high-resolution CT scans, and the nerves were demonstrated on MRI. DISCUSSION: To date, a few cases of narrow duplicate IAC have been reported in the literature, Approximately 20% of patients with congenital SNHL are found to show inner-ear bony abnormalities on CT, but much uncertainty still exists about the mechanism underlying IAC stenosis.(5) Imaging findings of the temporal bone in our case series demonstrated asymmetrical narrowing of both IACs, there is no clear evidence in the literature supporting the predominance of one side over the other. In our series, facial nerve function was intact bilaterally. As for our cases, both patients were enrolled in a single-sided deafness evaluation for a trial of options such as BAHA, CROS, cochlear implants, and other non-implantable hearing aids. Furthermore, addressing the important factors will optimize the outcomes including surgery at early age to optimize neural plasticity, with intense long-term therapy. CONCLUSION: Congenital duplication of the IAC likely convoying sensorineural hearing loss due to aplasia/hypoplasia of the vestibulocochlear nerve. Early diagnosis and intervention are essential to optimize patient outcomes. Elsevier 2022-04-20 /pmc/articles/PMC9121248/ /pubmed/35594789 http://dx.doi.org/10.1016/j.ijscr.2022.107109 Text en © 2022 The Authors 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 Series AlEnazi, Abdulaziz Saud Alshaiji, Abdulaziz Alenezi, Meaad Al-Sharydah, Abdulaziz Alsuhibani, Sari Alhaidey, Ali Samarah, Adnan AlQahtani, Munahi De novo sensorineural hearing loss sequelae of narrow, duplicated internal auditory canal: Case series and literature review |
title | De novo sensorineural hearing loss sequelae of narrow, duplicated internal auditory canal: Case series and literature review |
title_full | De novo sensorineural hearing loss sequelae of narrow, duplicated internal auditory canal: Case series and literature review |
title_fullStr | De novo sensorineural hearing loss sequelae of narrow, duplicated internal auditory canal: Case series and literature review |
title_full_unstemmed | De novo sensorineural hearing loss sequelae of narrow, duplicated internal auditory canal: Case series and literature review |
title_short | De novo sensorineural hearing loss sequelae of narrow, duplicated internal auditory canal: Case series and literature review |
title_sort | de novo sensorineural hearing loss sequelae of narrow, duplicated internal auditory canal: case series and literature review |
topic | Case Series |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9121248/ https://www.ncbi.nlm.nih.gov/pubmed/35594789 http://dx.doi.org/10.1016/j.ijscr.2022.107109 |
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