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Trigeminal hypoplasia due to vertebrobasilar dolichoectasia: A new entity

The term “vertebrobasilar dolichoectasia” refers to anomalous dilatation of the intracranial arteries associated with elongation or tortuosity of the affected vessels. The etiology of the disease is unknown and is usually detected incidentally. The predominant clinical manifestations arise due to th...

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Autores principales: Jha, Abhishek, Gupta, Prakhar, Haroon, Mohammad, Shah, Gaurav, Gupta, Gagan, Khalid, Mohd.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489062/
https://www.ncbi.nlm.nih.gov/pubmed/26167222
http://dx.doi.org/10.4103/1817-1745.159189
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author Jha, Abhishek
Gupta, Prakhar
Haroon, Mohammad
Shah, Gaurav
Gupta, Gagan
Khalid, Mohd.
author_facet Jha, Abhishek
Gupta, Prakhar
Haroon, Mohammad
Shah, Gaurav
Gupta, Gagan
Khalid, Mohd.
author_sort Jha, Abhishek
collection PubMed
description The term “vertebrobasilar dolichoectasia” refers to anomalous dilatation of the intracranial arteries associated with elongation or tortuosity of the affected vessels. The etiology of the disease is unknown and is usually detected incidentally. The predominant clinical manifestations arise due to the mass effect of the dilated vessels and may include cranial nerve compression, extrinsic aqueductal compression, motor and sensory disturbances. Trigeminal hypoplasia is a very uncommon condition, usually described in association with Goldenhar-Gorlin syndrome and has not yet been attributed to vertebrobasilar dolichoectasia. The current case report highlights this rare association of trigeminal nerve hypoplasia and vertebrobasilar dolichoectasia, leading to hemifacial and corneal anesthesia.
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spelling pubmed-44890622015-07-12 Trigeminal hypoplasia due to vertebrobasilar dolichoectasia: A new entity Jha, Abhishek Gupta, Prakhar Haroon, Mohammad Shah, Gaurav Gupta, Gagan Khalid, Mohd. J Pediatr Neurosci Case Report The term “vertebrobasilar dolichoectasia” refers to anomalous dilatation of the intracranial arteries associated with elongation or tortuosity of the affected vessels. The etiology of the disease is unknown and is usually detected incidentally. The predominant clinical manifestations arise due to the mass effect of the dilated vessels and may include cranial nerve compression, extrinsic aqueductal compression, motor and sensory disturbances. Trigeminal hypoplasia is a very uncommon condition, usually described in association with Goldenhar-Gorlin syndrome and has not yet been attributed to vertebrobasilar dolichoectasia. The current case report highlights this rare association of trigeminal nerve hypoplasia and vertebrobasilar dolichoectasia, leading to hemifacial and corneal anesthesia. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4489062/ /pubmed/26167222 http://dx.doi.org/10.4103/1817-1745.159189 Text en Copyright: © Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Jha, Abhishek
Gupta, Prakhar
Haroon, Mohammad
Shah, Gaurav
Gupta, Gagan
Khalid, Mohd.
Trigeminal hypoplasia due to vertebrobasilar dolichoectasia: A new entity
title Trigeminal hypoplasia due to vertebrobasilar dolichoectasia: A new entity
title_full Trigeminal hypoplasia due to vertebrobasilar dolichoectasia: A new entity
title_fullStr Trigeminal hypoplasia due to vertebrobasilar dolichoectasia: A new entity
title_full_unstemmed Trigeminal hypoplasia due to vertebrobasilar dolichoectasia: A new entity
title_short Trigeminal hypoplasia due to vertebrobasilar dolichoectasia: A new entity
title_sort trigeminal hypoplasia due to vertebrobasilar dolichoectasia: a new entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489062/
https://www.ncbi.nlm.nih.gov/pubmed/26167222
http://dx.doi.org/10.4103/1817-1745.159189
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