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Sudden Bilateral Sensorineural Hearing Loss Associated with HLA A1-B8-DR3 Haplotype
Sudden sensorineural hearing loss may be present as a symptom in systemic autoimmune diseases or may occur as a primary disorder without another organ involvement (autoimmune inner ear disease). The diagnosis of autoimmune inner ear disease is still predicated on clinical features, and to date speci...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782810/ https://www.ncbi.nlm.nih.gov/pubmed/24106629 http://dx.doi.org/10.1155/2013/590157 |
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author | Psillas, G. Daniilidis, M. Gerofotis, A. Veros, K. Vasilaki, A. Vital, I. Markou, K. |
author_facet | Psillas, G. Daniilidis, M. Gerofotis, A. Veros, K. Vasilaki, A. Vital, I. Markou, K. |
author_sort | Psillas, G. |
collection | PubMed |
description | Sudden sensorineural hearing loss may be present as a symptom in systemic autoimmune diseases or may occur as a primary disorder without another organ involvement (autoimmune inner ear disease). The diagnosis of autoimmune inner ear disease is still predicated on clinical features, and to date specific diagnostic tests are not available. We report a case of bilateral sudden hearing loss, tinnitus, intense rotatory vertigo, and nausea in a female patient in which the clinical manifestations, in addition to raised levels of circulating immune complexes, antithyroglobulin antibodies, and the presence of the HLA A1-B8-DR3 haplotype, allowed us to hypothesize an autoimmune inner ear disease. Cyclosporine-A immunosuppressive treatment in addition to steroids helped in hearing recovery that occurred progressively with normalization of the hearing function after a five-month treatment. Cyclosporine-A could be proposed as a therapeutic option in case of autoimmune inner ear disease allowing the suspension of corticosteroids that, at high dose, expose patients to potentially serious adverse events. |
format | Online Article Text |
id | pubmed-3782810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-37828102013-10-08 Sudden Bilateral Sensorineural Hearing Loss Associated with HLA A1-B8-DR3 Haplotype Psillas, G. Daniilidis, M. Gerofotis, A. Veros, K. Vasilaki, A. Vital, I. Markou, K. Case Rep Otolaryngol Case Report Sudden sensorineural hearing loss may be present as a symptom in systemic autoimmune diseases or may occur as a primary disorder without another organ involvement (autoimmune inner ear disease). The diagnosis of autoimmune inner ear disease is still predicated on clinical features, and to date specific diagnostic tests are not available. We report a case of bilateral sudden hearing loss, tinnitus, intense rotatory vertigo, and nausea in a female patient in which the clinical manifestations, in addition to raised levels of circulating immune complexes, antithyroglobulin antibodies, and the presence of the HLA A1-B8-DR3 haplotype, allowed us to hypothesize an autoimmune inner ear disease. Cyclosporine-A immunosuppressive treatment in addition to steroids helped in hearing recovery that occurred progressively with normalization of the hearing function after a five-month treatment. Cyclosporine-A could be proposed as a therapeutic option in case of autoimmune inner ear disease allowing the suspension of corticosteroids that, at high dose, expose patients to potentially serious adverse events. Hindawi Publishing Corporation 2013 2013-09-09 /pmc/articles/PMC3782810/ /pubmed/24106629 http://dx.doi.org/10.1155/2013/590157 Text en Copyright © 2013 G. Psillas et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Psillas, G. Daniilidis, M. Gerofotis, A. Veros, K. Vasilaki, A. Vital, I. Markou, K. Sudden Bilateral Sensorineural Hearing Loss Associated with HLA A1-B8-DR3 Haplotype |
title | Sudden Bilateral Sensorineural Hearing Loss Associated with HLA A1-B8-DR3 Haplotype |
title_full | Sudden Bilateral Sensorineural Hearing Loss Associated with HLA A1-B8-DR3 Haplotype |
title_fullStr | Sudden Bilateral Sensorineural Hearing Loss Associated with HLA A1-B8-DR3 Haplotype |
title_full_unstemmed | Sudden Bilateral Sensorineural Hearing Loss Associated with HLA A1-B8-DR3 Haplotype |
title_short | Sudden Bilateral Sensorineural Hearing Loss Associated with HLA A1-B8-DR3 Haplotype |
title_sort | sudden bilateral sensorineural hearing loss associated with hla a1-b8-dr3 haplotype |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782810/ https://www.ncbi.nlm.nih.gov/pubmed/24106629 http://dx.doi.org/10.1155/2013/590157 |
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