CC BY-NC-ND 4.0 · Annals of Otology and Neurotology 2022; 05(02): 073-077
DOI: 10.1055/s-0043-1764179
Original Article

Inner Ear Malformations in Cochlear Implantation Candidates at Mother and Child Hospital of Bingerville (Côte d’Ivoire)

Marie-Josée Tanon-Anoh
1   Department of Pediatric ENT, Mother and Child Hospital of Bingerville, Université Félix Houphouët-Boigny, Abidjan Riviera, Côte d’Ivoire
,
Esther K Badou-Nguessan
2   Department of ENT, Yopougon Teaching Hospital, Côte d’Ivoire
,
Olivier-Didier Zamblé Tra Bi
1   Department of Pediatric ENT, Mother and Child Hospital of Bingerville, Université Félix Houphouët-Boigny, Abidjan Riviera, Côte d’Ivoire
,
Corine M.A Assebian-Houenou
1   Department of Pediatric ENT, Mother and Child Hospital of Bingerville, Université Félix Houphouët-Boigny, Abidjan Riviera, Côte d’Ivoire
,
1   Department of Pediatric ENT, Mother and Child Hospital of Bingerville, Université Félix Houphouët-Boigny, Abidjan Riviera, Côte d’Ivoire
,
Yannick James Tatsitsa Langouo
2   Department of ENT, Yopougon Teaching Hospital, Côte d’Ivoire
› Author Affiliations

Abstract

Objective The aim of this study was to determine the prevalence and types of inner ear and/or cochlear nerve anomalies in children who are candidates for cochlear implantation.

Methods This was a descriptive cross-sectional study with a retrospective review of medical and imaging records performed in a tertiary care children's hospital. All cochlear implants candidates under 15 years old with imaging assessment between January 2019 and December 2021 were concerned. The studied parameters were reason for consultation, risks factors, inner ear malformations (IEMs) classified and stratified by sensorineural hearing loss (SNHL) degree, gender, and age at diagnosis.

Results In total, 81 children (162 ears) were included in the study. Abnormalities of the inner ear were found in nine children representing a prevalence of 11.1%. These children were aged between 2 and 14 years. The average age at diagnosis of SNHL was 3.5 years. Seven children had bilateral anomalies and two unilateral anomalies, that is, 16 ears presenting 40 malformations. These included 1 complete labyrinthine aplasia (2.5%), 12 cochlear malformations (30%), 1 common cavity (2.5%), 17 vestibular/squamous cell carcinoma (SCC) malformations (42.5%), and 5 internal auditory canal malformations (12.5%). Three ear out of 16 with abnormalities demonstrated a deficient cochlear nerve. There was an association between IEMs and profound deafness, and age at diagnosis of SNHL less than 2 years.

Conclusion This study shows that 11.1% of children with profound deafness have IEMs. SCC malformations and cochlear hypoplasia were the most common. A precise description of these malformations during the imaging assessment is particularly useful for cochlear implantation to better plan this surgery.



Publication History

Article published online:
26 May 2023

© 2023. Indian Society of Otology. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).

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