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Profiling intraoral neuropathic disturbances following lingual nerve injury and in burning mouth syndrome
BACKGROUND: The aim of the study was to analyse intraoral neurophysiological changes in patients with unilateral lingual nerve lesions as well as patients with Burning Mouth Syndrome (BMS) by applying a standardized Quantitative Sensory Testing (QST) protocol. METHODS: The study included patients su...
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/PMC5363027/ https://www.ncbi.nlm.nih.gov/pubmed/28330489 http://dx.doi.org/10.1186/s12903-017-0360-y |
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author | Hartmann, Amely Seeberger, Robin Bittner, Malte Rolke, Roman Welte-Jzyk, Claudia Daubländer, Monika |
author_facet | Hartmann, Amely Seeberger, Robin Bittner, Malte Rolke, Roman Welte-Jzyk, Claudia Daubländer, Monika |
author_sort | Hartmann, Amely |
collection | PubMed |
description | BACKGROUND: The aim of the study was to analyse intraoral neurophysiological changes in patients with unilateral lingual nerve lesions as well as patients with Burning Mouth Syndrome (BMS) by applying a standardized Quantitative Sensory Testing (QST) protocol. METHODS: The study included patients suffering from a peripheral lesion of the lingual nerve (n = 4), from BMS (n = 5) and healthy controls (n = 8). Neurophysiological tests were performed in the innervation areas of the tongue bilaterally. For BMS patients the dorsal foot area was used as reference. RESULTS: For patients with peripheral lesion of the lingual nerve the affected side of the tongue showed increased thresholds for thermal (p < 0.05–0.001) and mechanical (p < 0.01–0.001) QST parameters, indicating a hypoesthesia and thermal hypofunction. In BMS patients, a pinprick hypoalgesia (p < 0.001), a cold hyperalgesia (p < 0.01) and cold/warmth hypoesthesia (p < 0.01) could be detected. CONCLUSIONS: The results of this study verified the lingual nerve lesion in our patients as a peripheral dysfunction. The profile showed a loss of sensory function for small and large fibre mediated stimuli. A more differentiated classification of the lingual nerve injury was possible with QST, regarding profile, type and severity of the neurologic lesion. BMS could be seen as neuropathy with variable central and peripheral contributions among individuals resulting in chronic pain. |
format | Online Article Text |
id | pubmed-5363027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53630272017-03-24 Profiling intraoral neuropathic disturbances following lingual nerve injury and in burning mouth syndrome Hartmann, Amely Seeberger, Robin Bittner, Malte Rolke, Roman Welte-Jzyk, Claudia Daubländer, Monika BMC Oral Health Research Article BACKGROUND: The aim of the study was to analyse intraoral neurophysiological changes in patients with unilateral lingual nerve lesions as well as patients with Burning Mouth Syndrome (BMS) by applying a standardized Quantitative Sensory Testing (QST) protocol. METHODS: The study included patients suffering from a peripheral lesion of the lingual nerve (n = 4), from BMS (n = 5) and healthy controls (n = 8). Neurophysiological tests were performed in the innervation areas of the tongue bilaterally. For BMS patients the dorsal foot area was used as reference. RESULTS: For patients with peripheral lesion of the lingual nerve the affected side of the tongue showed increased thresholds for thermal (p < 0.05–0.001) and mechanical (p < 0.01–0.001) QST parameters, indicating a hypoesthesia and thermal hypofunction. In BMS patients, a pinprick hypoalgesia (p < 0.001), a cold hyperalgesia (p < 0.01) and cold/warmth hypoesthesia (p < 0.01) could be detected. CONCLUSIONS: The results of this study verified the lingual nerve lesion in our patients as a peripheral dysfunction. The profile showed a loss of sensory function for small and large fibre mediated stimuli. A more differentiated classification of the lingual nerve injury was possible with QST, regarding profile, type and severity of the neurologic lesion. BMS could be seen as neuropathy with variable central and peripheral contributions among individuals resulting in chronic pain. BioMed Central 2017-03-23 /pmc/articles/PMC5363027/ /pubmed/28330489 http://dx.doi.org/10.1186/s12903-017-0360-y 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 | Research Article Hartmann, Amely Seeberger, Robin Bittner, Malte Rolke, Roman Welte-Jzyk, Claudia Daubländer, Monika Profiling intraoral neuropathic disturbances following lingual nerve injury and in burning mouth syndrome |
title | Profiling intraoral neuropathic disturbances following lingual nerve injury and in burning mouth syndrome |
title_full | Profiling intraoral neuropathic disturbances following lingual nerve injury and in burning mouth syndrome |
title_fullStr | Profiling intraoral neuropathic disturbances following lingual nerve injury and in burning mouth syndrome |
title_full_unstemmed | Profiling intraoral neuropathic disturbances following lingual nerve injury and in burning mouth syndrome |
title_short | Profiling intraoral neuropathic disturbances following lingual nerve injury and in burning mouth syndrome |
title_sort | profiling intraoral neuropathic disturbances following lingual nerve injury and in burning mouth syndrome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363027/ https://www.ncbi.nlm.nih.gov/pubmed/28330489 http://dx.doi.org/10.1186/s12903-017-0360-y |
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