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Stylohyoid Complex Syndrome Associated With Unilateral Vocal Cord Palsy: A Case Report
Eagle’s syndrome is a rare cause of cervicofacial pain and is due to abnormalities in the stylohyoid process, stylohyoid ligament or lesser cornu of the hyoid bone. Generally, patients affected by Eagle’s syndrome present with pain in the lateral or upper neck, angle of the mandible, submandibular s...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8881992/ https://www.ncbi.nlm.nih.gov/pubmed/35233334 http://dx.doi.org/10.7759/cureus.21666 |
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author | Loroch, Anna Qamar, Sabih Nadeem Jaffer, Mehaab Smillie, Ian |
author_facet | Loroch, Anna Qamar, Sabih Nadeem Jaffer, Mehaab Smillie, Ian |
author_sort | Loroch, Anna |
collection | PubMed |
description | Eagle’s syndrome is a rare cause of cervicofacial pain and is due to abnormalities in the stylohyoid process, stylohyoid ligament or lesser cornu of the hyoid bone. Generally, patients affected by Eagle’s syndrome present with pain in the lateral or upper neck, angle of the mandible, submandibular space and throat (exacerbated by head movements and/or mastication); foreign body sensation; headache and referred otalgia. A 66-year old gentleman presented with a 36-month history of recurrent pain localising mainly to the right angle of the mandible and radiating to the submandibular triangle. No pathological changes were noted on multiple ultrasound scans. Flexible nasendoscopy revealed a right vocal cord palsy. Initially, the CT scan revealed an abnormality in the stylohyoid complex, and the patient was managed conservatively. Subsequent three-dimensional CT scan noted significant worsening of the abnormality in the stylohyoid complex. Due to progressive nature of the patient's symptoms and progression of stylohyoid complex calcification noted on imaging, the patient was listed for surgery. He underwent partial styloidectomy and vocal cord injection for cord paralysis secondary to impingement on the vagal nerve by the stylohyoid complex. The patient recovered well and denies any ongoing stylalgia. Various cases of Eagle’s syndrome have been managed successfully in a conservative manner. However, the authors of this case report suggest that patients with Eagle’s syndrome should be monitored closely. A delay in surgical intervention can lead to complications such as complete ossification of the stylohyoid complex and impingement on surrounding structures. This, in turn, increases intra-operative complexity. |
format | Online Article Text |
id | pubmed-8881992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-88819922022-02-28 Stylohyoid Complex Syndrome Associated With Unilateral Vocal Cord Palsy: A Case Report Loroch, Anna Qamar, Sabih Nadeem Jaffer, Mehaab Smillie, Ian Cureus Otolaryngology Eagle’s syndrome is a rare cause of cervicofacial pain and is due to abnormalities in the stylohyoid process, stylohyoid ligament or lesser cornu of the hyoid bone. Generally, patients affected by Eagle’s syndrome present with pain in the lateral or upper neck, angle of the mandible, submandibular space and throat (exacerbated by head movements and/or mastication); foreign body sensation; headache and referred otalgia. A 66-year old gentleman presented with a 36-month history of recurrent pain localising mainly to the right angle of the mandible and radiating to the submandibular triangle. No pathological changes were noted on multiple ultrasound scans. Flexible nasendoscopy revealed a right vocal cord palsy. Initially, the CT scan revealed an abnormality in the stylohyoid complex, and the patient was managed conservatively. Subsequent three-dimensional CT scan noted significant worsening of the abnormality in the stylohyoid complex. Due to progressive nature of the patient's symptoms and progression of stylohyoid complex calcification noted on imaging, the patient was listed for surgery. He underwent partial styloidectomy and vocal cord injection for cord paralysis secondary to impingement on the vagal nerve by the stylohyoid complex. The patient recovered well and denies any ongoing stylalgia. Various cases of Eagle’s syndrome have been managed successfully in a conservative manner. However, the authors of this case report suggest that patients with Eagle’s syndrome should be monitored closely. A delay in surgical intervention can lead to complications such as complete ossification of the stylohyoid complex and impingement on surrounding structures. This, in turn, increases intra-operative complexity. Cureus 2022-01-27 /pmc/articles/PMC8881992/ /pubmed/35233334 http://dx.doi.org/10.7759/cureus.21666 Text en Copyright © 2022, Loroch et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Otolaryngology Loroch, Anna Qamar, Sabih Nadeem Jaffer, Mehaab Smillie, Ian Stylohyoid Complex Syndrome Associated With Unilateral Vocal Cord Palsy: A Case Report |
title | Stylohyoid Complex Syndrome Associated With Unilateral Vocal Cord Palsy: A Case Report |
title_full | Stylohyoid Complex Syndrome Associated With Unilateral Vocal Cord Palsy: A Case Report |
title_fullStr | Stylohyoid Complex Syndrome Associated With Unilateral Vocal Cord Palsy: A Case Report |
title_full_unstemmed | Stylohyoid Complex Syndrome Associated With Unilateral Vocal Cord Palsy: A Case Report |
title_short | Stylohyoid Complex Syndrome Associated With Unilateral Vocal Cord Palsy: A Case Report |
title_sort | stylohyoid complex syndrome associated with unilateral vocal cord palsy: a case report |
topic | Otolaryngology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8881992/ https://www.ncbi.nlm.nih.gov/pubmed/35233334 http://dx.doi.org/10.7759/cureus.21666 |
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