» Articles » PMID: 32791649

[Immune-mediated Sensorineural Hearing Loss: Prevalence and Treatment Strategies]

Overview
Date 2020 Aug 14
PMID 32791649
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

Autoimmune sensorineural hearing loss is a rare clinical entity which accounting for less than 1% in all cases with hearing loss. The prevalence of hearing loss in immune-mediated inner ear diseases, as shown in case reports or single-center statistics, varies widely. We reviewed the current literatures on the association between sensorineural hearing loss and autoimmune diseases, focused on the prevalence of hearing loss in different autoimmune diseases, treatments and challenges.

Citing Articles

[Advances in the study of fluctuating sensorineural hearing loss].

Zhu Q, Zhang K, Zou S, Mao Q, Wang Q, Deng J Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2023; 37(3):238-242.

PMID: 36843527 PMC: 10320679. DOI: 10.13201/j.issn.2096-7993.2023.03.017.

References
1.
Aftab S, Semaan M, Murray G, Megerian C . Cochlear implantation outcomes in patients with autoimmune and immune-mediated inner ear disease. Otol Neurotol. 2010; 31(8):1337-42. DOI: 10.1097/MAO.0b013e3181f0c699. View

2.
Hu A, Parnes L . Intratympanic steroids for inner ear disorders: a review. Audiol Neurootol. 2009; 14(6):373-82. DOI: 10.1159/000241894. View

3.
Kastanioudakis I, Ziavra N, Politi E, Exarchakos G, Drosos A, Skevas A . Hearing loss in progressive systemic sclerosis patients: a comparative study. Otolaryngol Head Neck Surg. 2001; 124(5):522-5. DOI: 10.1067/mhn.2001.115092. View

4.
Trimarchi M, Sinico R, Teggi R, Bussi M, Specks U, Meroni P . Otorhinolaryngological manifestations in granulomatosis with polyangiitis (Wegener's). Autoimmun Rev. 2012; 12(4):501-5. DOI: 10.1016/j.autrev.2012.08.010. View

5.
Karabulut H, Dagli M, Ates A, Karaaslan Y . Results for audiology and distortion product and transient evoked otoacoustic emissions in patients with systemic lupus erythematosus. J Laryngol Otol. 2009; 124(2):137-40. DOI: 10.1017/S0022215109991332. View