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When paediatric facial nerve paralysis is not a Bell's palsy: A case of cerebellopontine angle tumour

Facial nerve paralysis in children is a rare clinical condition that can lead to serious complications. Due to their rare occurrence, tumours, especially in the cerebellopontine angle, may be overlooked. We report a case of cerebellopontine angle tumour in an 8-year-old boy who presented with a righ...

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Autores principales: Ismail, Meriam T., Rahman, Razlina A., Idris, Nur S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taibah University 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802848/
https://www.ncbi.nlm.nih.gov/pubmed/35140576
http://dx.doi.org/10.1016/j.jtumed.2021.08.008
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author Ismail, Meriam T.
Rahman, Razlina A.
Idris, Nur S.
author_facet Ismail, Meriam T.
Rahman, Razlina A.
Idris, Nur S.
author_sort Ismail, Meriam T.
collection PubMed
description Facial nerve paralysis in children is a rare clinical condition that can lead to serious complications. Due to their rare occurrence, tumours, especially in the cerebellopontine angle, may be overlooked. We report a case of cerebellopontine angle tumour in an 8-year-old boy who presented with a right-sided lower motor neuron type of facial nerve palsy. Further examination showed a mild bilateral nystagmus. However, misled by the initial diagnosis of Bell's palsy, there was a delay in performing diagnostic magnetic resonance imaging of the brain, which showed a large mass in the cerebellopontine. Subsequently, six weeks after his initial presentation, the boy succumbed to the disease. This case illustrates that careful clinical examination, even in a seemingly simple case, is imperative to avoid diagnostic errors.
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spelling pubmed-88028482022-02-08 When paediatric facial nerve paralysis is not a Bell's palsy: A case of cerebellopontine angle tumour Ismail, Meriam T. Rahman, Razlina A. Idris, Nur S. J Taibah Univ Med Sci Case Report Facial nerve paralysis in children is a rare clinical condition that can lead to serious complications. Due to their rare occurrence, tumours, especially in the cerebellopontine angle, may be overlooked. We report a case of cerebellopontine angle tumour in an 8-year-old boy who presented with a right-sided lower motor neuron type of facial nerve palsy. Further examination showed a mild bilateral nystagmus. However, misled by the initial diagnosis of Bell's palsy, there was a delay in performing diagnostic magnetic resonance imaging of the brain, which showed a large mass in the cerebellopontine. Subsequently, six weeks after his initial presentation, the boy succumbed to the disease. This case illustrates that careful clinical examination, even in a seemingly simple case, is imperative to avoid diagnostic errors. Taibah University 2021-09-04 /pmc/articles/PMC8802848/ /pubmed/35140576 http://dx.doi.org/10.1016/j.jtumed.2021.08.008 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Ismail, Meriam T.
Rahman, Razlina A.
Idris, Nur S.
When paediatric facial nerve paralysis is not a Bell's palsy: A case of cerebellopontine angle tumour
title When paediatric facial nerve paralysis is not a Bell's palsy: A case of cerebellopontine angle tumour
title_full When paediatric facial nerve paralysis is not a Bell's palsy: A case of cerebellopontine angle tumour
title_fullStr When paediatric facial nerve paralysis is not a Bell's palsy: A case of cerebellopontine angle tumour
title_full_unstemmed When paediatric facial nerve paralysis is not a Bell's palsy: A case of cerebellopontine angle tumour
title_short When paediatric facial nerve paralysis is not a Bell's palsy: A case of cerebellopontine angle tumour
title_sort when paediatric facial nerve paralysis is not a bell's palsy: a case of cerebellopontine angle tumour
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802848/
https://www.ncbi.nlm.nih.gov/pubmed/35140576
http://dx.doi.org/10.1016/j.jtumed.2021.08.008
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