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Intraarterial vasodilator therapy immediately rescued pure cortical deafness due to bilateral cerebral vasospasm
BACKGROUND: Cortical deafness is a rare symptom that is associated with bilateral lesions of the auditory cortex. To date, cortical deafness has been reported in only three cases of subarachnoid hemorrhage (SAH). CASE DESCRIPTION: This 55-year-old female was admitted to our hospital with SAH caused...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078451/ https://www.ncbi.nlm.nih.gov/pubmed/24991464 http://dx.doi.org/10.4103/2152-7806.132031 |
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author | Asakuno, Keizoh Ishida, Atsushi |
author_facet | Asakuno, Keizoh Ishida, Atsushi |
author_sort | Asakuno, Keizoh |
collection | PubMed |
description | BACKGROUND: Cortical deafness is a rare symptom that is associated with bilateral lesions of the auditory cortex. To date, cortical deafness has been reported in only three cases of subarachnoid hemorrhage (SAH). CASE DESCRIPTION: This 55-year-old female was admitted to our hospital with SAH caused by a ruptured left internal carotid artery (ICA) paraclinoid aneurysm. Computed tomography (CT) scans showed diffuse thick SAH with no other lesions such as an old infarction or hemorrhage. Emergent stent-assisted coil embolization was performed successfully and subsequent cisternal irrigation with urokinase almost completely washed out the thick SAH. During follow-up, she was alert and without any neurological deficits, however, she developed acute bilateral deafness on day 7 even though she had no history of hearing impairment. Because of the deafness, verbal communication was difficult. She became almost completely unable to hear and communication was confined to writing. Immediate diffusion-weighted (DW) image showed high intensities in bilateral superior temporal gyri due to severe vasospasm of bilateral middle cerebral arteries (MCAs). Immediate angiography showed severe vasospasm especially right MCA. A microcatheter was advanced to the right M1 and papaverine was administered. Soon after that, her hearing impairment dramatically improved. Our simple audiometry showed a hearing threshold average for both 1000 and 4000 Hz at 25 dB in both ears. She was discharged without any deficits in 2 weeks. CONCLUSIONS: To our knowledge, this is the first reported case of pure cortical deafness due to bilateral vasospasm, which was immediately resolved by intraarterial administration of papaverine. |
format | Online Article Text |
id | pubmed-4078451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-40784512014-07-02 Intraarterial vasodilator therapy immediately rescued pure cortical deafness due to bilateral cerebral vasospasm Asakuno, Keizoh Ishida, Atsushi Surg Neurol Int Case Report BACKGROUND: Cortical deafness is a rare symptom that is associated with bilateral lesions of the auditory cortex. To date, cortical deafness has been reported in only three cases of subarachnoid hemorrhage (SAH). CASE DESCRIPTION: This 55-year-old female was admitted to our hospital with SAH caused by a ruptured left internal carotid artery (ICA) paraclinoid aneurysm. Computed tomography (CT) scans showed diffuse thick SAH with no other lesions such as an old infarction or hemorrhage. Emergent stent-assisted coil embolization was performed successfully and subsequent cisternal irrigation with urokinase almost completely washed out the thick SAH. During follow-up, she was alert and without any neurological deficits, however, she developed acute bilateral deafness on day 7 even though she had no history of hearing impairment. Because of the deafness, verbal communication was difficult. She became almost completely unable to hear and communication was confined to writing. Immediate diffusion-weighted (DW) image showed high intensities in bilateral superior temporal gyri due to severe vasospasm of bilateral middle cerebral arteries (MCAs). Immediate angiography showed severe vasospasm especially right MCA. A microcatheter was advanced to the right M1 and papaverine was administered. Soon after that, her hearing impairment dramatically improved. Our simple audiometry showed a hearing threshold average for both 1000 and 4000 Hz at 25 dB in both ears. She was discharged without any deficits in 2 weeks. CONCLUSIONS: To our knowledge, this is the first reported case of pure cortical deafness due to bilateral vasospasm, which was immediately resolved by intraarterial administration of papaverine. Medknow Publications & Media Pvt Ltd 2014-05-06 /pmc/articles/PMC4078451/ /pubmed/24991464 http://dx.doi.org/10.4103/2152-7806.132031 Text en Copyright: © 2014 Asakuno K http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Case Report Asakuno, Keizoh Ishida, Atsushi Intraarterial vasodilator therapy immediately rescued pure cortical deafness due to bilateral cerebral vasospasm |
title | Intraarterial vasodilator therapy immediately rescued pure cortical deafness due to bilateral cerebral vasospasm |
title_full | Intraarterial vasodilator therapy immediately rescued pure cortical deafness due to bilateral cerebral vasospasm |
title_fullStr | Intraarterial vasodilator therapy immediately rescued pure cortical deafness due to bilateral cerebral vasospasm |
title_full_unstemmed | Intraarterial vasodilator therapy immediately rescued pure cortical deafness due to bilateral cerebral vasospasm |
title_short | Intraarterial vasodilator therapy immediately rescued pure cortical deafness due to bilateral cerebral vasospasm |
title_sort | intraarterial vasodilator therapy immediately rescued pure cortical deafness due to bilateral cerebral vasospasm |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078451/ https://www.ncbi.nlm.nih.gov/pubmed/24991464 http://dx.doi.org/10.4103/2152-7806.132031 |
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