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Creutzfeldt-Jakob disease presenting with bilateral hearing loss: A case report
BACKGROUND: Sporadic Creutzfeldt-Jakob disease (sCJD) is a prion disease characterized as a fatal transmissible neurodegenerative disorder. Dizziness is often the first presenting symptom of sCJD, but hearing loss as an early manifestation is very rare. CASE SUMMARY: A 76-year-old man presented with...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9254176/ https://www.ncbi.nlm.nih.gov/pubmed/35949824 http://dx.doi.org/10.12998/wjcc.v10.i18.6333 |
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author | Na, Seunghee Lee, Se A Lee, Jong Dae Lee, Eek-Sung Lee, Tae-Kyeong |
author_facet | Na, Seunghee Lee, Se A Lee, Jong Dae Lee, Eek-Sung Lee, Tae-Kyeong |
author_sort | Na, Seunghee |
collection | PubMed |
description | BACKGROUND: Sporadic Creutzfeldt-Jakob disease (sCJD) is a prion disease characterized as a fatal transmissible neurodegenerative disorder. Dizziness is often the first presenting symptom of sCJD, but hearing loss as an early manifestation is very rare. CASE SUMMARY: A 76-year-old man presented with bilateral sudden hearing impairment and dizziness for 10 d. He was taking medications for hypertension and diabetes. He denied any difficulty with activities of daily living or hearing impairment before the onset of symptoms. Pure tone audiometry showed bilateral severe hearing impairment. Brain magnetic resonance imaging (MRI) and laboratory tests were within normal limits. Given his diagnosis of sudden sensory hearing loss, the patient received corticosteroid treatment but it was ineffective. Two weeks later, he complained of aggravated gait impairment, disorientation, and cognitive impairment. Repeat brain MRI showed diffuse cortical high signal intensities on diffusion-weighted imaging. In cerebrospinal fluid analysis, the real-time quaking-induced conversion assay was positive, and 14-3-3 protein was detected in the by western blotting. Considering all the data, we diagnosed probable sCJD, and the patient’s symptoms rapidly progressed into akinetic mutism. CONCLUSION: For patients with abrupt bilateral hearing impairment, especially in the elderly, various differential diagnoses, including sCJD, should be considered. |
format | Online Article Text |
id | pubmed-9254176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-92541762022-08-09 Creutzfeldt-Jakob disease presenting with bilateral hearing loss: A case report Na, Seunghee Lee, Se A Lee, Jong Dae Lee, Eek-Sung Lee, Tae-Kyeong World J Clin Cases Case Report BACKGROUND: Sporadic Creutzfeldt-Jakob disease (sCJD) is a prion disease characterized as a fatal transmissible neurodegenerative disorder. Dizziness is often the first presenting symptom of sCJD, but hearing loss as an early manifestation is very rare. CASE SUMMARY: A 76-year-old man presented with bilateral sudden hearing impairment and dizziness for 10 d. He was taking medications for hypertension and diabetes. He denied any difficulty with activities of daily living or hearing impairment before the onset of symptoms. Pure tone audiometry showed bilateral severe hearing impairment. Brain magnetic resonance imaging (MRI) and laboratory tests were within normal limits. Given his diagnosis of sudden sensory hearing loss, the patient received corticosteroid treatment but it was ineffective. Two weeks later, he complained of aggravated gait impairment, disorientation, and cognitive impairment. Repeat brain MRI showed diffuse cortical high signal intensities on diffusion-weighted imaging. In cerebrospinal fluid analysis, the real-time quaking-induced conversion assay was positive, and 14-3-3 protein was detected in the by western blotting. Considering all the data, we diagnosed probable sCJD, and the patient’s symptoms rapidly progressed into akinetic mutism. CONCLUSION: For patients with abrupt bilateral hearing impairment, especially in the elderly, various differential diagnoses, including sCJD, should be considered. Baishideng Publishing Group Inc 2022-06-26 2022-06-26 /pmc/articles/PMC9254176/ /pubmed/35949824 http://dx.doi.org/10.12998/wjcc.v10.i18.6333 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Case Report Na, Seunghee Lee, Se A Lee, Jong Dae Lee, Eek-Sung Lee, Tae-Kyeong Creutzfeldt-Jakob disease presenting with bilateral hearing loss: A case report |
title | Creutzfeldt-Jakob disease presenting with bilateral hearing loss: A case report |
title_full | Creutzfeldt-Jakob disease presenting with bilateral hearing loss: A case report |
title_fullStr | Creutzfeldt-Jakob disease presenting with bilateral hearing loss: A case report |
title_full_unstemmed | Creutzfeldt-Jakob disease presenting with bilateral hearing loss: A case report |
title_short | Creutzfeldt-Jakob disease presenting with bilateral hearing loss: A case report |
title_sort | creutzfeldt-jakob disease presenting with bilateral hearing loss: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9254176/ https://www.ncbi.nlm.nih.gov/pubmed/35949824 http://dx.doi.org/10.12998/wjcc.v10.i18.6333 |
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