Photobiomodulation in the treatment of xerostomia associated with hyposalivation in a pediatric patient with systemic scleroderma
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.4322/acr.2020.220 http://hdl.handle.net/11449/207652 |
Resumo: | Scleroderma is a rare autoimmune disease characterized by excessive collagen production. The oral manifestations of the patient with scleroderma can include microstomia, xerostomia, and changes in the resorption teeth. We report the case of a 7-year-old female patient diagnosed with systemic scleroderma where photobiomodulation therapy was used to treat xerostomia associated with hyposalivation. She attended a pediatric clinic and presented with dry and rigid facial skin, trismus, xerostomia, malocclusion, and difficulty swallowing. Stimulated salivary flow was assessed before, during, and after treatment. Photobiomodulation therapy was conducted at four points at the sublingual glands with 660 nm, 100 mW, and 0.8 J/cm2 to each point; eight points at the parotid glands; and six points at the submandibular glands with 808 nm, 100 mW, and 0.8 J/cm2 for 8 seconds at each point. After this therapy, an increase in salivary flow, remission of the xerostomia, and an improvement in mastication and swallowing were observed. Photobiomodulation therapy was effective in controlling xerostomia in this pediatric patient, resulting in increased salivary flow and an improvement in her quality of life. |
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Photobiomodulation in the treatment of xerostomia associated with hyposalivation in a pediatric patient with systemic sclerodermaLaser therapyLow-level light therapyPediatricsSclerodermaSystemicXerostomiaScleroderma is a rare autoimmune disease characterized by excessive collagen production. The oral manifestations of the patient with scleroderma can include microstomia, xerostomia, and changes in the resorption teeth. We report the case of a 7-year-old female patient diagnosed with systemic scleroderma where photobiomodulation therapy was used to treat xerostomia associated with hyposalivation. She attended a pediatric clinic and presented with dry and rigid facial skin, trismus, xerostomia, malocclusion, and difficulty swallowing. Stimulated salivary flow was assessed before, during, and after treatment. Photobiomodulation therapy was conducted at four points at the sublingual glands with 660 nm, 100 mW, and 0.8 J/cm2 to each point; eight points at the parotid glands; and six points at the submandibular glands with 808 nm, 100 mW, and 0.8 J/cm2 for 8 seconds at each point. After this therapy, an increase in salivary flow, remission of the xerostomia, and an improvement in mastication and swallowing were observed. Photobiomodulation therapy was effective in controlling xerostomia in this pediatric patient, resulting in increased salivary flow and an improvement in her quality of life.Universidade Estadual de São Paulo (Unesp) Faculdade de Odontologia de Araraquara Departamento de Morfologia e Clínica InfantilUniversidade Estadual de São Paulo (Unesp) Faculdade de Odontologia de Araraquara Departamento de Diagnóstico e CirurgiaUniversidade Estadual de São Paulo (Unesp) Faculdade de Odontologia de Araraquara Departamento de Morfologia e Clínica InfantilUniversidade Estadual de São Paulo (Unesp) Faculdade de Odontologia de Araraquara Departamento de Diagnóstico e CirurgiaUniversidade Estadual Paulista (Unesp)De Oliveira, Analú Barros [UNESP]Ferrisse, Túlio Morandin [UNESP]Salomão, Karina Borges [UNESP]Miranda, Marina Lins [UNESP]Bufalino, Andreia [UNESP]Brighenti, Fernanda Lourenção [UNESP]2021-06-25T10:58:42Z2021-06-25T10:58:42Z2021-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.4322/acr.2020.220Autopsy and Case Reports, v. 11.2236-1960http://hdl.handle.net/11449/20765210.4322/acr.2020.2202-s2.0-85104827954Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengAutopsy and Case Reportsinfo:eu-repo/semantics/openAccess2024-09-26T15:22:04Zoai:repositorio.unesp.br:11449/207652Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-26T15:22:04Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Photobiomodulation in the treatment of xerostomia associated with hyposalivation in a pediatric patient with systemic scleroderma |
title |
Photobiomodulation in the treatment of xerostomia associated with hyposalivation in a pediatric patient with systemic scleroderma |
spellingShingle |
Photobiomodulation in the treatment of xerostomia associated with hyposalivation in a pediatric patient with systemic scleroderma De Oliveira, Analú Barros [UNESP] Laser therapy Low-level light therapy Pediatrics Scleroderma Systemic Xerostomia |
title_short |
Photobiomodulation in the treatment of xerostomia associated with hyposalivation in a pediatric patient with systemic scleroderma |
title_full |
Photobiomodulation in the treatment of xerostomia associated with hyposalivation in a pediatric patient with systemic scleroderma |
title_fullStr |
Photobiomodulation in the treatment of xerostomia associated with hyposalivation in a pediatric patient with systemic scleroderma |
title_full_unstemmed |
Photobiomodulation in the treatment of xerostomia associated with hyposalivation in a pediatric patient with systemic scleroderma |
title_sort |
Photobiomodulation in the treatment of xerostomia associated with hyposalivation in a pediatric patient with systemic scleroderma |
author |
De Oliveira, Analú Barros [UNESP] |
author_facet |
De Oliveira, Analú Barros [UNESP] Ferrisse, Túlio Morandin [UNESP] Salomão, Karina Borges [UNESP] Miranda, Marina Lins [UNESP] Bufalino, Andreia [UNESP] Brighenti, Fernanda Lourenção [UNESP] |
author_role |
author |
author2 |
Ferrisse, Túlio Morandin [UNESP] Salomão, Karina Borges [UNESP] Miranda, Marina Lins [UNESP] Bufalino, Andreia [UNESP] Brighenti, Fernanda Lourenção [UNESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
De Oliveira, Analú Barros [UNESP] Ferrisse, Túlio Morandin [UNESP] Salomão, Karina Borges [UNESP] Miranda, Marina Lins [UNESP] Bufalino, Andreia [UNESP] Brighenti, Fernanda Lourenção [UNESP] |
dc.subject.por.fl_str_mv |
Laser therapy Low-level light therapy Pediatrics Scleroderma Systemic Xerostomia |
topic |
Laser therapy Low-level light therapy Pediatrics Scleroderma Systemic Xerostomia |
description |
Scleroderma is a rare autoimmune disease characterized by excessive collagen production. The oral manifestations of the patient with scleroderma can include microstomia, xerostomia, and changes in the resorption teeth. We report the case of a 7-year-old female patient diagnosed with systemic scleroderma where photobiomodulation therapy was used to treat xerostomia associated with hyposalivation. She attended a pediatric clinic and presented with dry and rigid facial skin, trismus, xerostomia, malocclusion, and difficulty swallowing. Stimulated salivary flow was assessed before, during, and after treatment. Photobiomodulation therapy was conducted at four points at the sublingual glands with 660 nm, 100 mW, and 0.8 J/cm2 to each point; eight points at the parotid glands; and six points at the submandibular glands with 808 nm, 100 mW, and 0.8 J/cm2 for 8 seconds at each point. After this therapy, an increase in salivary flow, remission of the xerostomia, and an improvement in mastication and swallowing were observed. Photobiomodulation therapy was effective in controlling xerostomia in this pediatric patient, resulting in increased salivary flow and an improvement in her quality of life. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-06-25T10:58:42Z 2021-06-25T10:58:42Z 2021-01-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.4322/acr.2020.220 Autopsy and Case Reports, v. 11. 2236-1960 http://hdl.handle.net/11449/207652 10.4322/acr.2020.220 2-s2.0-85104827954 |
url |
http://dx.doi.org/10.4322/acr.2020.220 http://hdl.handle.net/11449/207652 |
identifier_str_mv |
Autopsy and Case Reports, v. 11. 2236-1960 10.4322/acr.2020.220 2-s2.0-85104827954 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Autopsy and Case Reports |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
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1813546486673178624 |