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Type a botulinum toxin in the management of spontaneous salivary otorrhea: a case report
BACKGROUND: Spontaneous salivary otorrhea is a rare presentation only previously documented twice in literature where parotid salivary secretions are found in the external auditory canal. Conventional treatment of spontaneous parotid salivary fistulas includes surgical management with interposed gra...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7424646/ https://www.ncbi.nlm.nih.gov/pubmed/32787918 http://dx.doi.org/10.1186/s40463-020-00457-y |
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author | Chan, Teffran J. Lewis, Trevor A. Sommer, Doron D. |
author_facet | Chan, Teffran J. Lewis, Trevor A. Sommer, Doron D. |
author_sort | Chan, Teffran J. |
collection | PubMed |
description | BACKGROUND: Spontaneous salivary otorrhea is a rare presentation only previously documented twice in literature where parotid salivary secretions are found in the external auditory canal. Conventional treatment of spontaneous parotid salivary fistulas includes surgical management with interposed grafts, fistula tract ablation, and possible superficial parotidectomy. Associated risks include facial nerve injury, Frey syndrome and facial scarring. Here we report the first case of spontaneous salivary otorrhea conservatively managed with a type A botulinum toxin (BTA) injection. CASE PRESENTATION: A 17-year-old female presented with a 5-month history of left sided otorrhea and transient left facial swelling associated with gustatory stimulation. The otorrhea fluid tested positive for salivary amylase and negative for beta 2 transferrin. Fifty units of BTA were injected into the left parotid gland under ultrasound guidance. Cessation of symptoms was achieved 3 weeks after intervention. The patient remains symptom-free at the 2 year follow up. CONCLUSION: BTA injection was well tolerated under ultrasound guidance and has led to long-term resolution of the patient’s symptoms. BTA injection appears to be a safe and effective way to conservatively manage this rare presentation of spontaneous salivary otorrhea. |
format | Online Article Text |
id | pubmed-7424646 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74246462020-08-16 Type a botulinum toxin in the management of spontaneous salivary otorrhea: a case report Chan, Teffran J. Lewis, Trevor A. Sommer, Doron D. J Otolaryngol Head Neck Surg Case Report BACKGROUND: Spontaneous salivary otorrhea is a rare presentation only previously documented twice in literature where parotid salivary secretions are found in the external auditory canal. Conventional treatment of spontaneous parotid salivary fistulas includes surgical management with interposed grafts, fistula tract ablation, and possible superficial parotidectomy. Associated risks include facial nerve injury, Frey syndrome and facial scarring. Here we report the first case of spontaneous salivary otorrhea conservatively managed with a type A botulinum toxin (BTA) injection. CASE PRESENTATION: A 17-year-old female presented with a 5-month history of left sided otorrhea and transient left facial swelling associated with gustatory stimulation. The otorrhea fluid tested positive for salivary amylase and negative for beta 2 transferrin. Fifty units of BTA were injected into the left parotid gland under ultrasound guidance. Cessation of symptoms was achieved 3 weeks after intervention. The patient remains symptom-free at the 2 year follow up. CONCLUSION: BTA injection was well tolerated under ultrasound guidance and has led to long-term resolution of the patient’s symptoms. BTA injection appears to be a safe and effective way to conservatively manage this rare presentation of spontaneous salivary otorrhea. BioMed Central 2020-08-12 /pmc/articles/PMC7424646/ /pubmed/32787918 http://dx.doi.org/10.1186/s40463-020-00457-y Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Case Report Chan, Teffran J. Lewis, Trevor A. Sommer, Doron D. Type a botulinum toxin in the management of spontaneous salivary otorrhea: a case report |
title | Type a botulinum toxin in the management of spontaneous salivary otorrhea: a case report |
title_full | Type a botulinum toxin in the management of spontaneous salivary otorrhea: a case report |
title_fullStr | Type a botulinum toxin in the management of spontaneous salivary otorrhea: a case report |
title_full_unstemmed | Type a botulinum toxin in the management of spontaneous salivary otorrhea: a case report |
title_short | Type a botulinum toxin in the management of spontaneous salivary otorrhea: a case report |
title_sort | type a botulinum toxin in the management of spontaneous salivary otorrhea: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7424646/ https://www.ncbi.nlm.nih.gov/pubmed/32787918 http://dx.doi.org/10.1186/s40463-020-00457-y |
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