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A rare case of bilateral cervical vagal neurofibromas: role of high-resolution ultrasound
BACKGROUND: Neurofibromas originating from vagus nerves are rarely reported in the literature. In particular, plexiform neurofibromas of the bilateral cervical vagus nerve are extremely rare. CASE PRESENTATION: A 21-year-old female presented with a 2-year history of swelling on the right side of her...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5294879/ https://www.ncbi.nlm.nih.gov/pubmed/28166752 http://dx.doi.org/10.1186/s12883-017-0806-5 |
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author | Liu, Bin Zhang, Yuanding Zhang, Lili Zhang, Fan Li, Hongyu Li, Shuang Liu, Yafang Du, Jie Zhao, Lirong |
author_facet | Liu, Bin Zhang, Yuanding Zhang, Lili Zhang, Fan Li, Hongyu Li, Shuang Liu, Yafang Du, Jie Zhao, Lirong |
author_sort | Liu, Bin |
collection | PubMed |
description | BACKGROUND: Neurofibromas originating from vagus nerves are rarely reported in the literature. In particular, plexiform neurofibromas of the bilateral cervical vagus nerve are extremely rare. CASE PRESENTATION: A 21-year-old female presented with a 2-year history of swelling on the right side of her neck. Physical examination revealed a soft-tissue mass on the right side of her neck. Ultrasonography (US) and magnetic resonance (MR) imaging showed a tumor centered in the right carotid sheath between the internal jugular vein and the common carotid artery. In addition, a similar nodular mass in the left carotid sheath was detected on US. The right mass was surgically resected; histopathological examination revealed a neurofibroma. CONCLUSIONS: US can be a valuable method for preoperative evaluation of cervical mass, as it is capable of displaying the vagus nerve and provides sufficient diagnostic information. The cervical vagal neurofibroma can manifest as solitary or multifocal lesion. Bilateral neurofibromas are usually associated with neurofibromatosis type 1 (NF1). Early diagnosis and prompt surgical treatment should be considered. |
format | Online Article Text |
id | pubmed-5294879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-52948792017-02-09 A rare case of bilateral cervical vagal neurofibromas: role of high-resolution ultrasound Liu, Bin Zhang, Yuanding Zhang, Lili Zhang, Fan Li, Hongyu Li, Shuang Liu, Yafang Du, Jie Zhao, Lirong BMC Neurol Case Report BACKGROUND: Neurofibromas originating from vagus nerves are rarely reported in the literature. In particular, plexiform neurofibromas of the bilateral cervical vagus nerve are extremely rare. CASE PRESENTATION: A 21-year-old female presented with a 2-year history of swelling on the right side of her neck. Physical examination revealed a soft-tissue mass on the right side of her neck. Ultrasonography (US) and magnetic resonance (MR) imaging showed a tumor centered in the right carotid sheath between the internal jugular vein and the common carotid artery. In addition, a similar nodular mass in the left carotid sheath was detected on US. The right mass was surgically resected; histopathological examination revealed a neurofibroma. CONCLUSIONS: US can be a valuable method for preoperative evaluation of cervical mass, as it is capable of displaying the vagus nerve and provides sufficient diagnostic information. The cervical vagal neurofibroma can manifest as solitary or multifocal lesion. Bilateral neurofibromas are usually associated with neurofibromatosis type 1 (NF1). Early diagnosis and prompt surgical treatment should be considered. BioMed Central 2017-02-06 /pmc/articles/PMC5294879/ /pubmed/28166752 http://dx.doi.org/10.1186/s12883-017-0806-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Liu, Bin Zhang, Yuanding Zhang, Lili Zhang, Fan Li, Hongyu Li, Shuang Liu, Yafang Du, Jie Zhao, Lirong A rare case of bilateral cervical vagal neurofibromas: role of high-resolution ultrasound |
title | A rare case of bilateral cervical vagal neurofibromas: role of high-resolution ultrasound |
title_full | A rare case of bilateral cervical vagal neurofibromas: role of high-resolution ultrasound |
title_fullStr | A rare case of bilateral cervical vagal neurofibromas: role of high-resolution ultrasound |
title_full_unstemmed | A rare case of bilateral cervical vagal neurofibromas: role of high-resolution ultrasound |
title_short | A rare case of bilateral cervical vagal neurofibromas: role of high-resolution ultrasound |
title_sort | rare case of bilateral cervical vagal neurofibromas: role of high-resolution ultrasound |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5294879/ https://www.ncbi.nlm.nih.gov/pubmed/28166752 http://dx.doi.org/10.1186/s12883-017-0806-5 |
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