Cargando…
Vertebrobasilar Dolichoectasia as a Rare Cause of Simultaneous Abducens and Vestibulocochlear Nerve Symptoms: A Case Report and Literature Review
Vertebrobasilar dolichoectasia (VBD) can lead to cranial nerve symptoms. However, multiple cranial nerve symptoms associated with VBD in one case remain extremely rare. We here present the case of a 33-year-old male with VBD diagnosed by multimodality imaging, who developed simultaneous abducens and...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7445531/ https://www.ncbi.nlm.nih.gov/pubmed/32903914 http://dx.doi.org/10.2147/IJGM.S269649 |
_version_ | 1783574008479875072 |
---|---|
author | Zang, Xuege Feng, Zheng Qiao, Hui Wang, Libo Fu, Chao |
author_facet | Zang, Xuege Feng, Zheng Qiao, Hui Wang, Libo Fu, Chao |
author_sort | Zang, Xuege |
collection | PubMed |
description | Vertebrobasilar dolichoectasia (VBD) can lead to cranial nerve symptoms. However, multiple cranial nerve symptoms associated with VBD in one case remain extremely rare. We here present the case of a 33-year-old male with VBD diagnosed by multimodality imaging, who developed simultaneous abducens and vestibulocochlear nerve symptoms and subsequently improved after blood pressure control treatment. To our knowledge, this is the first report of such a vascular disorder resulting in simultaneous symptoms of the abducens and vestibulocochlear nerves. This study highlights that such a vascular anomaly should be considered when cranial nerve symptom is encountered, especially when multiple cranial nerves involved. Meanwhile, radiological evalurrrrrrrrrrrrrrrrrrration of such neurovascular conflict using three-dimensional constructive interference in steady-state imaging is recommended. |
format | Online Article Text |
id | pubmed-7445531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-74455312020-09-04 Vertebrobasilar Dolichoectasia as a Rare Cause of Simultaneous Abducens and Vestibulocochlear Nerve Symptoms: A Case Report and Literature Review Zang, Xuege Feng, Zheng Qiao, Hui Wang, Libo Fu, Chao Int J Gen Med Case Report Vertebrobasilar dolichoectasia (VBD) can lead to cranial nerve symptoms. However, multiple cranial nerve symptoms associated with VBD in one case remain extremely rare. We here present the case of a 33-year-old male with VBD diagnosed by multimodality imaging, who developed simultaneous abducens and vestibulocochlear nerve symptoms and subsequently improved after blood pressure control treatment. To our knowledge, this is the first report of such a vascular disorder resulting in simultaneous symptoms of the abducens and vestibulocochlear nerves. This study highlights that such a vascular anomaly should be considered when cranial nerve symptom is encountered, especially when multiple cranial nerves involved. Meanwhile, radiological evalurrrrrrrrrrrrrrrrrrration of such neurovascular conflict using three-dimensional constructive interference in steady-state imaging is recommended. Dove 2020-08-20 /pmc/articles/PMC7445531/ /pubmed/32903914 http://dx.doi.org/10.2147/IJGM.S269649 Text en © 2020 Zang et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Case Report Zang, Xuege Feng, Zheng Qiao, Hui Wang, Libo Fu, Chao Vertebrobasilar Dolichoectasia as a Rare Cause of Simultaneous Abducens and Vestibulocochlear Nerve Symptoms: A Case Report and Literature Review |
title | Vertebrobasilar Dolichoectasia as a Rare Cause of Simultaneous Abducens and Vestibulocochlear Nerve Symptoms: A Case Report and Literature Review |
title_full | Vertebrobasilar Dolichoectasia as a Rare Cause of Simultaneous Abducens and Vestibulocochlear Nerve Symptoms: A Case Report and Literature Review |
title_fullStr | Vertebrobasilar Dolichoectasia as a Rare Cause of Simultaneous Abducens and Vestibulocochlear Nerve Symptoms: A Case Report and Literature Review |
title_full_unstemmed | Vertebrobasilar Dolichoectasia as a Rare Cause of Simultaneous Abducens and Vestibulocochlear Nerve Symptoms: A Case Report and Literature Review |
title_short | Vertebrobasilar Dolichoectasia as a Rare Cause of Simultaneous Abducens and Vestibulocochlear Nerve Symptoms: A Case Report and Literature Review |
title_sort | vertebrobasilar dolichoectasia as a rare cause of simultaneous abducens and vestibulocochlear nerve symptoms: a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7445531/ https://www.ncbi.nlm.nih.gov/pubmed/32903914 http://dx.doi.org/10.2147/IJGM.S269649 |
work_keys_str_mv | AT zangxuege vertebrobasilardolichoectasiaasararecauseofsimultaneousabducensandvestibulocochlearnervesymptomsacasereportandliteraturereview AT fengzheng vertebrobasilardolichoectasiaasararecauseofsimultaneousabducensandvestibulocochlearnervesymptomsacasereportandliteraturereview AT qiaohui vertebrobasilardolichoectasiaasararecauseofsimultaneousabducensandvestibulocochlearnervesymptomsacasereportandliteraturereview AT wanglibo vertebrobasilardolichoectasiaasararecauseofsimultaneousabducensandvestibulocochlearnervesymptomsacasereportandliteraturereview AT fuchao vertebrobasilardolichoectasiaasararecauseofsimultaneousabducensandvestibulocochlearnervesymptomsacasereportandliteraturereview |