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Vocal cord paralysis secondary to spontaneous internal carotid dissection: case report and systematic review of the literature

OBJECTIVES: To present a rare case of unilateral vocal cord paralysis (VCP) secondary to spontaneous internal carotid artery dissection and to perform a literature review. CASE REPORT: A 35-year-old male presented to the emergency department with acute onset hoarseness and dysphagia. History, physic...

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Autores principales: Nguyen, TT Jean, Zhang, Han, Dziegielewski, Peter T, Seemann, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660211/
https://www.ncbi.nlm.nih.gov/pubmed/23668480
http://dx.doi.org/10.1186/1916-0216-42-34
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author Nguyen, TT Jean
Zhang, Han
Dziegielewski, Peter T
Seemann, Robert
author_facet Nguyen, TT Jean
Zhang, Han
Dziegielewski, Peter T
Seemann, Robert
author_sort Nguyen, TT Jean
collection PubMed
description OBJECTIVES: To present a rare case of unilateral vocal cord paralysis (VCP) secondary to spontaneous internal carotid artery dissection and to perform a literature review. CASE REPORT: A 35-year-old male presented to the emergency department with acute onset hoarseness and dysphagia. History, physical exam and laryngoscopy revealed left sided VCP without obvious cause. Magnetic Resonance Imaging (MRI) demonstrated a left internal carotid artery dissection of unknown etiology. Neurovascular surgery was consulted and treatment with aspirin was initiated. The dysphagia and hoarseness resolved in 12 weeks with long-term neurosurgery follow-up as the management plan. METHODS: Systematic literature review was conducted by 3 independent reviewers. Since 1988 only 9 cases of VCP due to internal carotid artery dissection have been reported. These were reviewed for: demographics, diagnostic method, treatment and vocal cord function. RESULTS: 7 patients had unilateral while 2 had bilateral VCP. MRI was used for diagnosis in 7 cases and 5 cases utilized a type of angiography. All received antithrombotic treatment with 5 out of the 9 patients experiencing vocal cord recovery in an average of 7.2 weeks. CONCLUSION: MRI is crucial in the work-up of idiopathic VCP. If an ipsilateral internal carotid artery dissection is found, antithrombotic treatment is initiated with an expectation that vocal cord mobility is likely to return.
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spelling pubmed-36602112013-05-23 Vocal cord paralysis secondary to spontaneous internal carotid dissection: case report and systematic review of the literature Nguyen, TT Jean Zhang, Han Dziegielewski, Peter T Seemann, Robert J Otolaryngol Head Neck Surg Case Report OBJECTIVES: To present a rare case of unilateral vocal cord paralysis (VCP) secondary to spontaneous internal carotid artery dissection and to perform a literature review. CASE REPORT: A 35-year-old male presented to the emergency department with acute onset hoarseness and dysphagia. History, physical exam and laryngoscopy revealed left sided VCP without obvious cause. Magnetic Resonance Imaging (MRI) demonstrated a left internal carotid artery dissection of unknown etiology. Neurovascular surgery was consulted and treatment with aspirin was initiated. The dysphagia and hoarseness resolved in 12 weeks with long-term neurosurgery follow-up as the management plan. METHODS: Systematic literature review was conducted by 3 independent reviewers. Since 1988 only 9 cases of VCP due to internal carotid artery dissection have been reported. These were reviewed for: demographics, diagnostic method, treatment and vocal cord function. RESULTS: 7 patients had unilateral while 2 had bilateral VCP. MRI was used for diagnosis in 7 cases and 5 cases utilized a type of angiography. All received antithrombotic treatment with 5 out of the 9 patients experiencing vocal cord recovery in an average of 7.2 weeks. CONCLUSION: MRI is crucial in the work-up of idiopathic VCP. If an ipsilateral internal carotid artery dissection is found, antithrombotic treatment is initiated with an expectation that vocal cord mobility is likely to return. BioMed Central 2013-05-13 /pmc/articles/PMC3660211/ /pubmed/23668480 http://dx.doi.org/10.1186/1916-0216-42-34 Text en Copyright © 2013 Nguyen 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
Nguyen, TT Jean
Zhang, Han
Dziegielewski, Peter T
Seemann, Robert
Vocal cord paralysis secondary to spontaneous internal carotid dissection: case report and systematic review of the literature
title Vocal cord paralysis secondary to spontaneous internal carotid dissection: case report and systematic review of the literature
title_full Vocal cord paralysis secondary to spontaneous internal carotid dissection: case report and systematic review of the literature
title_fullStr Vocal cord paralysis secondary to spontaneous internal carotid dissection: case report and systematic review of the literature
title_full_unstemmed Vocal cord paralysis secondary to spontaneous internal carotid dissection: case report and systematic review of the literature
title_short Vocal cord paralysis secondary to spontaneous internal carotid dissection: case report and systematic review of the literature
title_sort vocal cord paralysis secondary to spontaneous internal carotid dissection: case report and systematic review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660211/
https://www.ncbi.nlm.nih.gov/pubmed/23668480
http://dx.doi.org/10.1186/1916-0216-42-34
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