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Percheron thalamopeduncular syndrome with cervical dystonia: A case report

Bilateral thalamic infarctions are usually caused by occlusion of the "Artery of Percheron" (AoP). Thalamopeduncular syndrome is among the most common presentations of AoP occlusion. A 59-year-old male presented abrupt decreased level of consciousness. After several weeks, on regaining con...

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Autores principales: Vasconcellos, Luiz Felipe, Tiel, Chan, Sudo, Felipe Kenji, Moreira, Denise Madeira, Engelhardt, Eliasz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação de Neurologia Cognitiva e do Comportamento 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5619280/
https://www.ncbi.nlm.nih.gov/pubmed/29213484
http://dx.doi.org/10.1590/s1980-5764-2016dn1004019
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author Vasconcellos, Luiz Felipe
Tiel, Chan
Sudo, Felipe Kenji
Moreira, Denise Madeira
Engelhardt, Eliasz
author_facet Vasconcellos, Luiz Felipe
Tiel, Chan
Sudo, Felipe Kenji
Moreira, Denise Madeira
Engelhardt, Eliasz
author_sort Vasconcellos, Luiz Felipe
collection PubMed
description Bilateral thalamic infarctions are usually caused by occlusion of the "Artery of Percheron" (AoP). Thalamopeduncular syndrome is among the most common presentations of AoP occlusion. A 59-year-old male presented abrupt decreased level of consciousness. After several weeks, on regaining consciousness, he exhibited oculomotor abnormalities, ataxic gait, cervical dystonia, and cognitive and behavioral changes. Magnetic resonance imaging disclosed thalamic, subthalamic, mammillary and midbrain infarction. Clinical features suggestive of bilateral thalamopeduncular syndrome were identified. Besides the presence of cognitive impairment and behavioral symptoms, cervical dystonia was evident, possibly resulting from interruption of the interconnections among basal ganglia, thalamus, subthalamus, midbrain and cerebellum.
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spelling pubmed-56192802017-12-06 Percheron thalamopeduncular syndrome with cervical dystonia: A case report Vasconcellos, Luiz Felipe Tiel, Chan Sudo, Felipe Kenji Moreira, Denise Madeira Engelhardt, Eliasz Dement Neuropsychol Case Report Bilateral thalamic infarctions are usually caused by occlusion of the "Artery of Percheron" (AoP). Thalamopeduncular syndrome is among the most common presentations of AoP occlusion. A 59-year-old male presented abrupt decreased level of consciousness. After several weeks, on regaining consciousness, he exhibited oculomotor abnormalities, ataxic gait, cervical dystonia, and cognitive and behavioral changes. Magnetic resonance imaging disclosed thalamic, subthalamic, mammillary and midbrain infarction. Clinical features suggestive of bilateral thalamopeduncular syndrome were identified. Besides the presence of cognitive impairment and behavioral symptoms, cervical dystonia was evident, possibly resulting from interruption of the interconnections among basal ganglia, thalamus, subthalamus, midbrain and cerebellum. Associação de Neurologia Cognitiva e do Comportamento 2016 /pmc/articles/PMC5619280/ /pubmed/29213484 http://dx.doi.org/10.1590/s1980-5764-2016dn1004019 Text en http://creativecommons.org/licenses/by/4.0/ 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 work is properly cited.
spellingShingle Case Report
Vasconcellos, Luiz Felipe
Tiel, Chan
Sudo, Felipe Kenji
Moreira, Denise Madeira
Engelhardt, Eliasz
Percheron thalamopeduncular syndrome with cervical dystonia: A case report
title Percheron thalamopeduncular syndrome with cervical dystonia: A case report
title_full Percheron thalamopeduncular syndrome with cervical dystonia: A case report
title_fullStr Percheron thalamopeduncular syndrome with cervical dystonia: A case report
title_full_unstemmed Percheron thalamopeduncular syndrome with cervical dystonia: A case report
title_short Percheron thalamopeduncular syndrome with cervical dystonia: A case report
title_sort percheron thalamopeduncular syndrome with cervical dystonia: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5619280/
https://www.ncbi.nlm.nih.gov/pubmed/29213484
http://dx.doi.org/10.1590/s1980-5764-2016dn1004019
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