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An unexpected case of Ramsay hunt syndrome: case report and literature review
BACKGROUND: Ramsay Hunt Syndrome (RHS) is a rare, severe complication of varicella zoster virus (VZV) reactivation in the geniculate ganglion. Facial paralysis is one of the features and without treatment, it fully recovers in as little as 20% of cases; this is much improved if treatment is started...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3847606/ https://www.ncbi.nlm.nih.gov/pubmed/23985267 http://dx.doi.org/10.1186/1756-0500-6-337 |
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author | Worme, Mali Chada, Reena Lavallee, Lilia |
author_facet | Worme, Mali Chada, Reena Lavallee, Lilia |
author_sort | Worme, Mali |
collection | PubMed |
description | BACKGROUND: Ramsay Hunt Syndrome (RHS) is a rare, severe complication of varicella zoster virus (VZV) reactivation in the geniculate ganglion. Facial paralysis is one of the features and without treatment, it fully recovers in as little as 20% of cases; this is much improved if treatment is started within 72 hours. This case is noteworthy in that coexistence of facial palsy with cervical dermatome involvement by VZV is not typical of RHS. Yet, it has been reported before. CASE PRESENTATION: A 54 year old Caucasian woman presented with right ear discomfort, difficulty hearing and a vesicular rash along the pinnae, 8 days after the eruption of a similar rash in the right C2-C4 dermatomes. 2 days later, she awoke with a partial right-sided facial paralysis, which improved with treatment (valacyclovir and prednisone). CONCLUSIONS: This case is most pertinent to Family Practice, Otolaryngology and Neurology. It highlights the possible co-existence of RHS with cervical VZV reactivation and encourages physicians to monitor for this complication even before geniculate ganglion reactivation occurs. RHS is a rare disease that can present with vague symptoms. A high index of suspicion and close follow up are essential. Early intervention with antivirals and corticosteroids has shown significantly improved outcomes in these patients. |
format | Online Article Text |
id | pubmed-3847606 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38476062013-12-04 An unexpected case of Ramsay hunt syndrome: case report and literature review Worme, Mali Chada, Reena Lavallee, Lilia BMC Res Notes Case Report BACKGROUND: Ramsay Hunt Syndrome (RHS) is a rare, severe complication of varicella zoster virus (VZV) reactivation in the geniculate ganglion. Facial paralysis is one of the features and without treatment, it fully recovers in as little as 20% of cases; this is much improved if treatment is started within 72 hours. This case is noteworthy in that coexistence of facial palsy with cervical dermatome involvement by VZV is not typical of RHS. Yet, it has been reported before. CASE PRESENTATION: A 54 year old Caucasian woman presented with right ear discomfort, difficulty hearing and a vesicular rash along the pinnae, 8 days after the eruption of a similar rash in the right C2-C4 dermatomes. 2 days later, she awoke with a partial right-sided facial paralysis, which improved with treatment (valacyclovir and prednisone). CONCLUSIONS: This case is most pertinent to Family Practice, Otolaryngology and Neurology. It highlights the possible co-existence of RHS with cervical VZV reactivation and encourages physicians to monitor for this complication even before geniculate ganglion reactivation occurs. RHS is a rare disease that can present with vague symptoms. A high index of suspicion and close follow up are essential. Early intervention with antivirals and corticosteroids has shown significantly improved outcomes in these patients. BioMed Central 2013-08-28 /pmc/articles/PMC3847606/ /pubmed/23985267 http://dx.doi.org/10.1186/1756-0500-6-337 Text en Copyright © 2013 Worme et al.; 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 cited. |
spellingShingle | Case Report Worme, Mali Chada, Reena Lavallee, Lilia An unexpected case of Ramsay hunt syndrome: case report and literature review |
title | An unexpected case of Ramsay hunt syndrome: case report and literature review |
title_full | An unexpected case of Ramsay hunt syndrome: case report and literature review |
title_fullStr | An unexpected case of Ramsay hunt syndrome: case report and literature review |
title_full_unstemmed | An unexpected case of Ramsay hunt syndrome: case report and literature review |
title_short | An unexpected case of Ramsay hunt syndrome: case report and literature review |
title_sort | unexpected case of ramsay hunt syndrome: case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3847606/ https://www.ncbi.nlm.nih.gov/pubmed/23985267 http://dx.doi.org/10.1186/1756-0500-6-337 |
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