Cargando…

Facial nerve compression by the posterior inferior cerebellar artery causing facial pain and swelling: a case report

INTRODUCTION: We report an unusual case of facial pain and swelling caused by compression of the facial and vestibulocochlear cranial nerves due to the tortuous course of a branch of the posterior inferior cerebellar artery. Although anterior inferior cerebellar artery compression has been well docu...

Descripción completa

Detalles Bibliográficos
Autores principales: Batten, Rebecca L, Ng, Wan-Fai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4018959/
https://www.ncbi.nlm.nih.gov/pubmed/24661509
http://dx.doi.org/10.1186/1752-1947-8-105
_version_ 1782480131402498048
author Batten, Rebecca L
Ng, Wan-Fai
author_facet Batten, Rebecca L
Ng, Wan-Fai
author_sort Batten, Rebecca L
collection PubMed
description INTRODUCTION: We report an unusual case of facial pain and swelling caused by compression of the facial and vestibulocochlear cranial nerves due to the tortuous course of a branch of the posterior inferior cerebellar artery. Although anterior inferior cerebellar artery compression has been well documented in the literature, compression caused by the posterior inferior cerebellar artery is rare. This case provided a diagnostic dilemma, requiring expertise from a number of specialties, and proved to be a learning point to clinicians from a variety of backgrounds. We describe the case in detail and discuss the differential diagnoses. CASE PRESENTATION: A 57-year-old Caucasian woman with a background of mild connective tissue disease presented to our rheumatologist with intermittent left-sided facial pain and swelling, accompanied by hearing loss in her left ear. An autoimmune screen was negative and a Schirmer’s test was normal. Her erythrocyte sedimentation rate was 6mm/h (normal range: 1 to 20mm/h) and her immunoglobulin G and A levels were mildly elevated. A vascular loop protocol magnetic resonance imaging scan showed a loop of her posterior inferior cerebellar artery taking a long course around the seventh and eighth cranial nerves into the meatus and back, resulting in compression of her seventh and eighth cranial nerves. Our patient underwent microvascular decompression, after which her symptoms completely resolved. CONCLUSION: Hemifacial spasm is characterized by unilateral clonic twitching, although our patient presented with more unusual symptoms of pain and swelling. Onset of symptoms is mostly in middle age and women are more commonly affected. Differential diagnoses include trigeminal neuralgia, temporomandibular joint dysfunction, salivary gland pathology and migrainous headache. Botulinum toxin injection is recognized as an effective treatment option for primary hemifacial spasm. Microvascular decompression is a relatively safe procedure with a high success rate. Although a rare pathology, posterior inferior cerebellar artery compression causing facial pain, swelling and hearing loss should be considered as a differential diagnosis in similar cases.
format Online
Article
Text
id pubmed-4018959
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-40189592014-05-14 Facial nerve compression by the posterior inferior cerebellar artery causing facial pain and swelling: a case report Batten, Rebecca L Ng, Wan-Fai J Med Case Rep Case Report INTRODUCTION: We report an unusual case of facial pain and swelling caused by compression of the facial and vestibulocochlear cranial nerves due to the tortuous course of a branch of the posterior inferior cerebellar artery. Although anterior inferior cerebellar artery compression has been well documented in the literature, compression caused by the posterior inferior cerebellar artery is rare. This case provided a diagnostic dilemma, requiring expertise from a number of specialties, and proved to be a learning point to clinicians from a variety of backgrounds. We describe the case in detail and discuss the differential diagnoses. CASE PRESENTATION: A 57-year-old Caucasian woman with a background of mild connective tissue disease presented to our rheumatologist with intermittent left-sided facial pain and swelling, accompanied by hearing loss in her left ear. An autoimmune screen was negative and a Schirmer’s test was normal. Her erythrocyte sedimentation rate was 6mm/h (normal range: 1 to 20mm/h) and her immunoglobulin G and A levels were mildly elevated. A vascular loop protocol magnetic resonance imaging scan showed a loop of her posterior inferior cerebellar artery taking a long course around the seventh and eighth cranial nerves into the meatus and back, resulting in compression of her seventh and eighth cranial nerves. Our patient underwent microvascular decompression, after which her symptoms completely resolved. CONCLUSION: Hemifacial spasm is characterized by unilateral clonic twitching, although our patient presented with more unusual symptoms of pain and swelling. Onset of symptoms is mostly in middle age and women are more commonly affected. Differential diagnoses include trigeminal neuralgia, temporomandibular joint dysfunction, salivary gland pathology and migrainous headache. Botulinum toxin injection is recognized as an effective treatment option for primary hemifacial spasm. Microvascular decompression is a relatively safe procedure with a high success rate. Although a rare pathology, posterior inferior cerebellar artery compression causing facial pain, swelling and hearing loss should be considered as a differential diagnosis in similar cases. BioMed Central 2014-03-25 /pmc/articles/PMC4018959/ /pubmed/24661509 http://dx.doi.org/10.1186/1752-1947-8-105 Text en Copyright © 2014 Batten and Ng; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Batten, Rebecca L
Ng, Wan-Fai
Facial nerve compression by the posterior inferior cerebellar artery causing facial pain and swelling: a case report
title Facial nerve compression by the posterior inferior cerebellar artery causing facial pain and swelling: a case report
title_full Facial nerve compression by the posterior inferior cerebellar artery causing facial pain and swelling: a case report
title_fullStr Facial nerve compression by the posterior inferior cerebellar artery causing facial pain and swelling: a case report
title_full_unstemmed Facial nerve compression by the posterior inferior cerebellar artery causing facial pain and swelling: a case report
title_short Facial nerve compression by the posterior inferior cerebellar artery causing facial pain and swelling: a case report
title_sort facial nerve compression by the posterior inferior cerebellar artery causing facial pain and swelling: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4018959/
https://www.ncbi.nlm.nih.gov/pubmed/24661509
http://dx.doi.org/10.1186/1752-1947-8-105
work_keys_str_mv AT battenrebeccal facialnervecompressionbytheposteriorinferiorcerebellararterycausingfacialpainandswellingacasereport
AT ngwanfai facialnervecompressionbytheposteriorinferiorcerebellararterycausingfacialpainandswellingacasereport