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Mutism resulting from heterochronic bilateral cerebellar hemorrhages – A case report
BACKGROUND: Cerebellar mutism (CM) is a neurological condition characterized by lack of speech due to cerebellar lesions. Interruption of the bilateral dentatothalamocortical (DTC) pathways at midline structure seems the principal cause of CM but not fully understood. We described a rare case of CM...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6744780/ https://www.ncbi.nlm.nih.gov/pubmed/31528458 http://dx.doi.org/10.25259/SNI-18-2019 |
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author | Katsuki, Masahito Narisawa, Ayumi Karibe, Hiroshi Kameyama, Motonobu Tominaga, Teiji |
author_facet | Katsuki, Masahito Narisawa, Ayumi Karibe, Hiroshi Kameyama, Motonobu Tominaga, Teiji |
author_sort | Katsuki, Masahito |
collection | PubMed |
description | BACKGROUND: Cerebellar mutism (CM) is a neurological condition characterized by lack of speech due to cerebellar lesions. Interruption of the bilateral dentatothalamocortical (DTC) pathways at midline structure seems the principal cause of CM but not fully understood. We described a rare case of CM due to heterochronic bilateral cerebellar hemorrhages. CASE DESCRIPTION: An 87-year-old woman presented with depression of alertness after sudden vomiting. Neurologically, mild dysmetria and mutism were observed. The head computed tomography (CT) showed both a fresh right cerebellar hemorrhage and an obsolete left one. The patient was diagnosed as CM since both the thalamus and the supplementary motor area were bilaterally intact on both CT and magnetic resonance imaging. Medical treatment and rehabilitation improved her ataxia and ambulation. She became cognitively alert and could communicate by nodding, shaking her head, or facial expression. However, her mutism did not change at 4 months after the stroke. CONCLUSION: There are few reports on CM due to direct injuries to the bilateral dentate nuclei. Since our case did not show any injury other than bilateral dentate nuclei, this report can support the hypothesis that the interruptions of the bilateral DTC are the cause of CM. |
format | Online Article Text |
id | pubmed-6744780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-67447802019-09-16 Mutism resulting from heterochronic bilateral cerebellar hemorrhages – A case report Katsuki, Masahito Narisawa, Ayumi Karibe, Hiroshi Kameyama, Motonobu Tominaga, Teiji Surg Neurol Int Case Report BACKGROUND: Cerebellar mutism (CM) is a neurological condition characterized by lack of speech due to cerebellar lesions. Interruption of the bilateral dentatothalamocortical (DTC) pathways at midline structure seems the principal cause of CM but not fully understood. We described a rare case of CM due to heterochronic bilateral cerebellar hemorrhages. CASE DESCRIPTION: An 87-year-old woman presented with depression of alertness after sudden vomiting. Neurologically, mild dysmetria and mutism were observed. The head computed tomography (CT) showed both a fresh right cerebellar hemorrhage and an obsolete left one. The patient was diagnosed as CM since both the thalamus and the supplementary motor area were bilaterally intact on both CT and magnetic resonance imaging. Medical treatment and rehabilitation improved her ataxia and ambulation. She became cognitively alert and could communicate by nodding, shaking her head, or facial expression. However, her mutism did not change at 4 months after the stroke. CONCLUSION: There are few reports on CM due to direct injuries to the bilateral dentate nuclei. Since our case did not show any injury other than bilateral dentate nuclei, this report can support the hypothesis that the interruptions of the bilateral DTC are the cause of CM. Scientific Scholar 2019-06-25 /pmc/articles/PMC6744780/ /pubmed/31528458 http://dx.doi.org/10.25259/SNI-18-2019 Text en Copyright: © 2019 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Katsuki, Masahito Narisawa, Ayumi Karibe, Hiroshi Kameyama, Motonobu Tominaga, Teiji Mutism resulting from heterochronic bilateral cerebellar hemorrhages – A case report |
title | Mutism resulting from heterochronic bilateral cerebellar hemorrhages – A case report |
title_full | Mutism resulting from heterochronic bilateral cerebellar hemorrhages – A case report |
title_fullStr | Mutism resulting from heterochronic bilateral cerebellar hemorrhages – A case report |
title_full_unstemmed | Mutism resulting from heterochronic bilateral cerebellar hemorrhages – A case report |
title_short | Mutism resulting from heterochronic bilateral cerebellar hemorrhages – A case report |
title_sort | mutism resulting from heterochronic bilateral cerebellar hemorrhages – a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6744780/ https://www.ncbi.nlm.nih.gov/pubmed/31528458 http://dx.doi.org/10.25259/SNI-18-2019 |
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