Intraosseous neurofibroma versus schwannoma, importance of histological differential diagnosis in the definitive diagnosis: Case report

Detalhes bibliográficos
Autor(a) principal: Silva, André Gustavo Góes da
Data de Publicação: 2021
Outros Autores: Genú, Paloma Rodrigues, Cardoso, Antônio Jorge Orestes, Neves, Riedel Frota Sá Nogueira, Soares, Cauê Fontan, Lima Júnior, Miquéias Oliveira de
Tipo de documento: Artigo
Idioma: por
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/15025
Resumo: Neoplasms of neural origin represent 8% and 12% of all malignant and benign soft tissue neoplasms, respectively. In this group, tumors of the peripheral nerve sheath (TBNP) are inserted, a relatively rare group of diseases that are classified according to the specific characteristics of differentiation, cellular components and extracellular matrix. Neurofibroma and schwannoma are examples of lesions belonging to this group. The objective of this study is to present a clinical case of a female patient, 60 years old, diagnosed with a central lesion in the region of the right mandibular body. The lesion was discovered after a routine examination for prosthetic rehabilitation and, after incisional biopsy, initial diagnosis of schwannoma was obtained. The proposed treatment was a marginal resection, through the installation of a 2.4mm reconstruction plate and enucleation of the lesion. An escisional biopsy was then requested where neurofibroma was obtained as the final diagnosis. The patient had a satisfactory response to treatment, with no signs of recurrence. Although the decisive diagnosis of neurofibroma is based on histological findings, lesions such as schwannoma should be included as a differential histological diagnosis, which can hinder the definitive diagnosis. In this sense, peculiar characteristics of schwannoma and neurofibroma, their immunohistochemical behaviors and their similarities are necessary to trace their repercussions in establishing the diagnosis. Although there is no difference in treatment, such injuries may be associated which makes their final differentiation necessary, specifically for cases in which there is doubt.
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spelling Intraosseous neurofibroma versus schwannoma, importance of histological differential diagnosis in the definitive diagnosis: Case reportNeurofibroma intraóseo versus schwannoma, importancia del diagnóstico diferencial histológico en el diagnóstico definitivo: Relato de casoNeurofibroma intraósseo versus schwannoma, importância do diagnóstico diferencial histológico no diagnóstico definitivo: Relato de casoSchwannomaNeurofibromaDiagnosis.SchwannomaNeurofibromaDiagnóstico.SchwannomaNeurofibromaDiagnóstico.Neoplasms of neural origin represent 8% and 12% of all malignant and benign soft tissue neoplasms, respectively. In this group, tumors of the peripheral nerve sheath (TBNP) are inserted, a relatively rare group of diseases that are classified according to the specific characteristics of differentiation, cellular components and extracellular matrix. Neurofibroma and schwannoma are examples of lesions belonging to this group. The objective of this study is to present a clinical case of a female patient, 60 years old, diagnosed with a central lesion in the region of the right mandibular body. The lesion was discovered after a routine examination for prosthetic rehabilitation and, after incisional biopsy, initial diagnosis of schwannoma was obtained. The proposed treatment was a marginal resection, through the installation of a 2.4mm reconstruction plate and enucleation of the lesion. An escisional biopsy was then requested where neurofibroma was obtained as the final diagnosis. The patient had a satisfactory response to treatment, with no signs of recurrence. Although the decisive diagnosis of neurofibroma is based on histological findings, lesions such as schwannoma should be included as a differential histological diagnosis, which can hinder the definitive diagnosis. In this sense, peculiar characteristics of schwannoma and neurofibroma, their immunohistochemical behaviors and their similarities are necessary to trace their repercussions in establishing the diagnosis. Although there is no difference in treatment, such injuries may be associated which makes their final differentiation necessary, specifically for cases in which there is doubt.Las neoplasias neurales de origen neural representan el 8% y el 12% de todas las neoplasias malignas y benignas de       tejidos blandos, respectivamente. En este conjunto se insertan los tumores de la vaina del nervio periférico (TBNP), un grupo relativamente raro de enfermedades que se clasifican según las características específicas de diferenciación, componentes celulares y matriz extracelular. El neurofibroma y el schwannoma son ejemplos de lesiones pertenecientes a este grupo. El objetivo de este estudio es presentar el caso clínico de una paciente de 60 años diagnosticada de lesión central en la región del cuerpo mandibular derecho. La lesión fue descubierta tras un examen de rutina para rehabilitación protésica y, tras biopsia incisional, se obtuvo el diagnóstico inicial de schwannoma. El tratamiento propuesto fue una resección marginal, mediante la instalación de una placa de recontrucción de 2,4 mm y enucleación de la lesión. Luego se solicitó una biopsia por escisión donde se obtuvo como diagnosticó final neurofibroma.  El paciente tuvo una respuesta satisfactoria al tratamiento, sin signos de recidiva. Aunque el diagnóstico decisivo de neurofibroma se basa en hallazgos histológicos, lesiones como el schwannoma deben incluirse como diagnóstico histológico diferencial, que puede dificultar el diagnóstico definitivo. En este sentido, las características peculiares del schwannoma y neurofibroma, sus comportamientos inmunohistoquímicos y sus similitudes son necesarias para rastrear sus repercusiones en el establecimiento del diagnóstico. Aunque no existe diferencia de tratamiento, dichas lesiones pueden estar asociadas a diferentes síndromes, lo que hace necesaria su diferenciación final, específicamente para los casos en los que existe duda.As neoplasias de origem neurais representam 8% e 12% de todas as neoplasias de tecidos moles malignas e benignas, respectivamente. Nesse conjunto estão inseridos os tumores da bainha do nervo periférico (TBNP), um grupo relativamente raro de doenças que são classificadas de acordo com as características específicas de diferenciação, componentes celulares e matriz extracelular. Neurofibroma e schwannoma são exemplos de lesões pertencentes a esse grupo. O objetivo desse estudo é apresentar um caso clínico de uma paciente, sexo feminino, 60 anos de idade, diagnosticada com lesão central na região de corpo mandibular direito. A lesão foi descoberta após exame de rotina para reabilitação protética e, após biopsia incisional, obteve-se diagnóstico inicial de schwannoma. O tratamento proposto foi uma ressecção marginal, por meio da instalação de placa de reconstrução de 2,4mm e enucleação da lesão. Uma biopsia excisional foi então solicitada onde se obteve como diagnóstico final neurofibroma. A paciente apresentou resposta satisfatória ao tratamento, sem sinais de recidiva. Embora o diagnóstico decisivo de neurofibroma seja baseado em achados histológicos, lesões como schwannoma devem ser incluídas como diagnóstico diferencial histológico, o que pode dificultar o diagnóstico definitivo. Nesse sentido, características peculiares do schwannoma e neurofibroma, seus comportamentos imunoistoquímicos e suas semelhanças são necessários para traçar suas repercussões no estabelecimento do diagnóstico. Ainda que não haja diferença no tratamento, tais lesões podem estar associadas a síndromes diferentes, o que torna necessária sua diferenciação final, especificamente para os casos em que haja dúvida.Research, Society and Development2021-05-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/1502510.33448/rsd-v10i5.15025Research, Society and Development; Vol. 10 No. 5; e32010515025Research, Society and Development; Vol. 10 Núm. 5; e32010515025Research, Society and Development; v. 10 n. 5; e320105150252525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/15025/13440Copyright (c) 2021 André Gustavo Góes da Silva; Paloma Rodrigues Genú; Antônio Jorge Orestes Cardoso; Riedel Frota Sá Nogueira Neves; Cauê Fontan Soares; Miquéias Oliveira de Lima Júniorhttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessSilva, André Gustavo Góes daGenú, Paloma RodriguesCardoso, Antônio Jorge OrestesNeves, Riedel Frota Sá NogueiraSoares, Cauê FontanLima Júnior, Miquéias Oliveira de2021-05-17T18:20:49Zoai:ojs.pkp.sfu.ca:article/15025Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:35:57.386501Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Intraosseous neurofibroma versus schwannoma, importance of histological differential diagnosis in the definitive diagnosis: Case report
Neurofibroma intraóseo versus schwannoma, importancia del diagnóstico diferencial histológico en el diagnóstico definitivo: Relato de caso
Neurofibroma intraósseo versus schwannoma, importância do diagnóstico diferencial histológico no diagnóstico definitivo: Relato de caso
title Intraosseous neurofibroma versus schwannoma, importance of histological differential diagnosis in the definitive diagnosis: Case report
spellingShingle Intraosseous neurofibroma versus schwannoma, importance of histological differential diagnosis in the definitive diagnosis: Case report
Silva, André Gustavo Góes da
Schwannoma
Neurofibroma
Diagnosis.
Schwannoma
Neurofibroma
Diagnóstico.
Schwannoma
Neurofibroma
Diagnóstico.
title_short Intraosseous neurofibroma versus schwannoma, importance of histological differential diagnosis in the definitive diagnosis: Case report
title_full Intraosseous neurofibroma versus schwannoma, importance of histological differential diagnosis in the definitive diagnosis: Case report
title_fullStr Intraosseous neurofibroma versus schwannoma, importance of histological differential diagnosis in the definitive diagnosis: Case report
title_full_unstemmed Intraosseous neurofibroma versus schwannoma, importance of histological differential diagnosis in the definitive diagnosis: Case report
title_sort Intraosseous neurofibroma versus schwannoma, importance of histological differential diagnosis in the definitive diagnosis: Case report
author Silva, André Gustavo Góes da
author_facet Silva, André Gustavo Góes da
Genú, Paloma Rodrigues
Cardoso, Antônio Jorge Orestes
Neves, Riedel Frota Sá Nogueira
Soares, Cauê Fontan
Lima Júnior, Miquéias Oliveira de
author_role author
author2 Genú, Paloma Rodrigues
Cardoso, Antônio Jorge Orestes
Neves, Riedel Frota Sá Nogueira
Soares, Cauê Fontan
Lima Júnior, Miquéias Oliveira de
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Silva, André Gustavo Góes da
Genú, Paloma Rodrigues
Cardoso, Antônio Jorge Orestes
Neves, Riedel Frota Sá Nogueira
Soares, Cauê Fontan
Lima Júnior, Miquéias Oliveira de
dc.subject.por.fl_str_mv Schwannoma
Neurofibroma
Diagnosis.
Schwannoma
Neurofibroma
Diagnóstico.
Schwannoma
Neurofibroma
Diagnóstico.
topic Schwannoma
Neurofibroma
Diagnosis.
Schwannoma
Neurofibroma
Diagnóstico.
Schwannoma
Neurofibroma
Diagnóstico.
description Neoplasms of neural origin represent 8% and 12% of all malignant and benign soft tissue neoplasms, respectively. In this group, tumors of the peripheral nerve sheath (TBNP) are inserted, a relatively rare group of diseases that are classified according to the specific characteristics of differentiation, cellular components and extracellular matrix. Neurofibroma and schwannoma are examples of lesions belonging to this group. The objective of this study is to present a clinical case of a female patient, 60 years old, diagnosed with a central lesion in the region of the right mandibular body. The lesion was discovered after a routine examination for prosthetic rehabilitation and, after incisional biopsy, initial diagnosis of schwannoma was obtained. The proposed treatment was a marginal resection, through the installation of a 2.4mm reconstruction plate and enucleation of the lesion. An escisional biopsy was then requested where neurofibroma was obtained as the final diagnosis. The patient had a satisfactory response to treatment, with no signs of recurrence. Although the decisive diagnosis of neurofibroma is based on histological findings, lesions such as schwannoma should be included as a differential histological diagnosis, which can hinder the definitive diagnosis. In this sense, peculiar characteristics of schwannoma and neurofibroma, their immunohistochemical behaviors and their similarities are necessary to trace their repercussions in establishing the diagnosis. Although there is no difference in treatment, such injuries may be associated which makes their final differentiation necessary, specifically for cases in which there is doubt.
publishDate 2021
dc.date.none.fl_str_mv 2021-05-08
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10.33448/rsd-v10i5.15025
url https://rsdjournal.org/index.php/rsd/article/view/15025
identifier_str_mv 10.33448/rsd-v10i5.15025
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/15025/13440
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Research, Society and Development
publisher.none.fl_str_mv Research, Society and Development
dc.source.none.fl_str_mv Research, Society and Development; Vol. 10 No. 5; e32010515025
Research, Society and Development; Vol. 10 Núm. 5; e32010515025
Research, Society and Development; v. 10 n. 5; e32010515025
2525-3409
reponame:Research, Society and Development
instname:Universidade Federal de Itajubá (UNIFEI)
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instname_str Universidade Federal de Itajubá (UNIFEI)
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institution UNIFEI
reponame_str Research, Society and Development
collection Research, Society and Development
repository.name.fl_str_mv Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)
repository.mail.fl_str_mv rsd.articles@gmail.com
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