Systemic Lupus Erythemathosus and Oral Lichen Planus overlap syndrome: case report

Detalhes bibliográficos
Autor(a) principal: Lira, Rafaela Martins
Data de Publicação: 2022
Outros Autores: Oliveira, Catarina Rodrigues Rosa de, Kotovicz, Leticia Bandeira de Melo, Omena, Andréa Magalhães Agra de, Abreu, Eulina Maria Vieira de, Ferreira, Sonia Maria Soares
Tipo de documento: Artigo
Idioma: por
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/28978
Resumo: The Overlap Syndrome (OS) associated with Systemic Lupus Erythematosus (SLE) and Lichen Planus (LP), a rare entity, is characterized by a clinical and immunohistopathological signs of both. We report the case of a 39-year-old female patient diagnosed with SLE, presenting with intraoral lesions whose diagnostic hypotheses were Oral Lichen Planus (OLP) and SLE. In this scenario, the present study aimed to describe the pathologies mentioned, as well as to expose the difficulties of the diagnostic process of the overlap syndrome in question, explaining the stages of the disease and the treatment performed. The work was carried out through a case study with descriptive objectives and a qualitative approach using clinical knowledge of dermatology, stomatology and rheumatology, based on bibliographic research and integrative literature review in digital databases with the analysis of complementary, histopathological and immunofluorescence exams. In the biopsy of clinically ambiguous lesions, as in the case of the patient's oral lesions, histopathological features of one or both processes can be found simultaneously or fluctuating at different times, making diagnosis difficult and complicating prognosis and treatment. Thus, it was observed that direct immunofluorescence (DIF) has become an essential tool to aid in the diagnosis of this condition. This case reinforces that OS has a challenging diagnosis and its treatment involves several professionals to manage it.
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spelling Systemic Lupus Erythemathosus and Oral Lichen Planus overlap syndrome: case reportSíndrome de superposición de Lúpus Eritematoso Sistémico y Liquen Plano Oral: reporte de casoSíndrome de sobreposição de Lúpus Eritematoso Sistêmico e Líquen Plano Oral: relato de casoSindrome de superposiciónLúpus Eritematoso SistémicoLiquen PlanoEnseñanza.Síndrome de SobreposiçãoLúpus Eritematoso SistêmicoLíquen PlanoEnsino.Overlap SyndromeSystemic Lupus ErythematosusLichen PlanusTeaching.The Overlap Syndrome (OS) associated with Systemic Lupus Erythematosus (SLE) and Lichen Planus (LP), a rare entity, is characterized by a clinical and immunohistopathological signs of both. We report the case of a 39-year-old female patient diagnosed with SLE, presenting with intraoral lesions whose diagnostic hypotheses were Oral Lichen Planus (OLP) and SLE. In this scenario, the present study aimed to describe the pathologies mentioned, as well as to expose the difficulties of the diagnostic process of the overlap syndrome in question, explaining the stages of the disease and the treatment performed. The work was carried out through a case study with descriptive objectives and a qualitative approach using clinical knowledge of dermatology, stomatology and rheumatology, based on bibliographic research and integrative literature review in digital databases with the analysis of complementary, histopathological and immunofluorescence exams. In the biopsy of clinically ambiguous lesions, as in the case of the patient's oral lesions, histopathological features of one or both processes can be found simultaneously or fluctuating at different times, making diagnosis difficult and complicating prognosis and treatment. Thus, it was observed that direct immunofluorescence (DIF) has become an essential tool to aid in the diagnosis of this condition. This case reinforces that OS has a challenging diagnosis and its treatment involves several professionals to manage it.El Síndrome de Superposición (SS) asociado a Lupus Eritematoso Sistémico (LES) y Liquen Plano (LP), una entidad rara, se caracteriza por signos clínicos e inmunohistopatológicos sincrónicos de ambos. Presentamos el caso de una paciente de 39 años diagnosticada de LES, que presenta lesiones intraorales cuyas hipótesis diagnósticas fueron Liquen Plano Oral (LPO) y LES. En ese escenario, el presente estudio tuvo como objetivo describir las patologías mencionadas, así como exponer las dificultades del proceso diagnóstico del síndrome de superposición en cuestión, explicando las etapas de la enfermedad y el tratamiento realizado. El trabajo se realizó a través de un estudio de caso con objetivos descriptivos y un enfoque cualitativo utilizando conocimientos clínicos de dermatología, estomatología y reumatología, a partir de la investigación bibliográfica y revisión integradora de literatura en bases de datos digitales junto con el análisis de exámenes complementarios, histopatológicos y pruebas de inmunofluorescencia. En la biopsia de lesiones clínicamente ambiguas, como es el caso de las lesiones orales del paciente, se pueden encontrar características histopatológicas de uno o ambos procesos simultáneamente o fluctuantes en diferentes momentos, lo que dificulta el diagnóstico y complica el pronóstico y el tratamiento. Así, se observó que la inmunofluorescencia directa (DIF) se ha convertido en una herramienta esencial para ayudar en el diagnóstico de esta condición. Este caso refuerza que el SS tiene un diagnóstico desafiante y su tratamiento involucra a varios profesionales para manejarlo.A Síndrome de Sobreposição (SS) associada ao Lúpus Eritematoso Sistêmico (LES) e Líquen Plano (LP), entidade rara, é caracterizada por sinais clínicos e imuno-histopatológicos sincrônicos de ambos. Relatamos o caso de uma paciente do sexo feminino, 39 anos, com diagnóstico de LES, apresentando lesões intraorais cujas hipóteses diagnósticas foram Líquen Plano Oral (LPO) e LES. Neste cenário, o presente estudo teve como objetivo descrever as patologias citadas, assim como expor as dificuldades do processo diagnóstico da síndrome de sobreposição em questão, explanando as etapas da doença e o tratamento realizado. O trabalho foi realizado através de um estudo de caso com objetivos descritivos e abordagem qualitativa utilizando-se de conhecimentos clínicos da dermatologia, estomatologia e reumatologia, com base em pesquisa bibliográfica e revisão de literatura integrativa em bases de dados digitais juntamente com a análise de exames complementares, histopatológicos e de imunofluoerescência. Na biópsia de lesões clinicamente ambíguas, como no caso das lesões orais da paciente, características histopatológicas de um ou ambos os processos podem ser encontrados simultaneamente ou oscilando em períodos diferentes, dificultando o diagnóstico e complicando o prognóstico e tratamento. Assim, foi observado que a imunofluorescência direta (IFD) tornou-se uma ferramenta essencial para auxiliar no diagnóstico dessa condição. Este caso reforça que a SS possui um diagnóstico desafiador e seu tratamento envolve vários profissionais para gerenciá-la.  Research, Society and Development2022-04-26info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/2897810.33448/rsd-v11i6.28978Research, Society and Development; Vol. 11 No. 6; e23911628978Research, Society and Development; Vol. 11 Núm. 6; e23911628978Research, Society and Development; v. 11 n. 6; e239116289782525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/28978/25168Copyright (c) 2022 Rafaela Martins Lira; Catarina Rodrigues Rosa de Oliveira; Leticia Bandeira de Melo Kotovicz; Andréa Magalhães Agra de Omena; Eulina Maria Vieira de Abreu; Sonia Maria Soares Ferreirahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessLira, Rafaela Martins Oliveira, Catarina Rodrigues Rosa deKotovicz, Leticia Bandeira de Melo Omena, Andréa Magalhães Agra deAbreu, Eulina Maria Vieira deFerreira, Sonia Maria Soares 2022-05-13T18:04:10Zoai:ojs.pkp.sfu.ca:article/28978Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:46:11.468481Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Systemic Lupus Erythemathosus and Oral Lichen Planus overlap syndrome: case report
Síndrome de superposición de Lúpus Eritematoso Sistémico y Liquen Plano Oral: reporte de caso
Síndrome de sobreposição de Lúpus Eritematoso Sistêmico e Líquen Plano Oral: relato de caso
title Systemic Lupus Erythemathosus and Oral Lichen Planus overlap syndrome: case report
spellingShingle Systemic Lupus Erythemathosus and Oral Lichen Planus overlap syndrome: case report
Lira, Rafaela Martins
Sindrome de superposición
Lúpus Eritematoso Sistémico
Liquen Plano
Enseñanza.
Síndrome de Sobreposição
Lúpus Eritematoso Sistêmico
Líquen Plano
Ensino.
Overlap Syndrome
Systemic Lupus Erythematosus
Lichen Planus
Teaching.
title_short Systemic Lupus Erythemathosus and Oral Lichen Planus overlap syndrome: case report
title_full Systemic Lupus Erythemathosus and Oral Lichen Planus overlap syndrome: case report
title_fullStr Systemic Lupus Erythemathosus and Oral Lichen Planus overlap syndrome: case report
title_full_unstemmed Systemic Lupus Erythemathosus and Oral Lichen Planus overlap syndrome: case report
title_sort Systemic Lupus Erythemathosus and Oral Lichen Planus overlap syndrome: case report
author Lira, Rafaela Martins
author_facet Lira, Rafaela Martins
Oliveira, Catarina Rodrigues Rosa de
Kotovicz, Leticia Bandeira de Melo
Omena, Andréa Magalhães Agra de
Abreu, Eulina Maria Vieira de
Ferreira, Sonia Maria Soares
author_role author
author2 Oliveira, Catarina Rodrigues Rosa de
Kotovicz, Leticia Bandeira de Melo
Omena, Andréa Magalhães Agra de
Abreu, Eulina Maria Vieira de
Ferreira, Sonia Maria Soares
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Lira, Rafaela Martins
Oliveira, Catarina Rodrigues Rosa de
Kotovicz, Leticia Bandeira de Melo
Omena, Andréa Magalhães Agra de
Abreu, Eulina Maria Vieira de
Ferreira, Sonia Maria Soares
dc.subject.por.fl_str_mv Sindrome de superposición
Lúpus Eritematoso Sistémico
Liquen Plano
Enseñanza.
Síndrome de Sobreposição
Lúpus Eritematoso Sistêmico
Líquen Plano
Ensino.
Overlap Syndrome
Systemic Lupus Erythematosus
Lichen Planus
Teaching.
topic Sindrome de superposición
Lúpus Eritematoso Sistémico
Liquen Plano
Enseñanza.
Síndrome de Sobreposição
Lúpus Eritematoso Sistêmico
Líquen Plano
Ensino.
Overlap Syndrome
Systemic Lupus Erythematosus
Lichen Planus
Teaching.
description The Overlap Syndrome (OS) associated with Systemic Lupus Erythematosus (SLE) and Lichen Planus (LP), a rare entity, is characterized by a clinical and immunohistopathological signs of both. We report the case of a 39-year-old female patient diagnosed with SLE, presenting with intraoral lesions whose diagnostic hypotheses were Oral Lichen Planus (OLP) and SLE. In this scenario, the present study aimed to describe the pathologies mentioned, as well as to expose the difficulties of the diagnostic process of the overlap syndrome in question, explaining the stages of the disease and the treatment performed. The work was carried out through a case study with descriptive objectives and a qualitative approach using clinical knowledge of dermatology, stomatology and rheumatology, based on bibliographic research and integrative literature review in digital databases with the analysis of complementary, histopathological and immunofluorescence exams. In the biopsy of clinically ambiguous lesions, as in the case of the patient's oral lesions, histopathological features of one or both processes can be found simultaneously or fluctuating at different times, making diagnosis difficult and complicating prognosis and treatment. Thus, it was observed that direct immunofluorescence (DIF) has become an essential tool to aid in the diagnosis of this condition. This case reinforces that OS has a challenging diagnosis and its treatment involves several professionals to manage it.
publishDate 2022
dc.date.none.fl_str_mv 2022-04-26
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/28978
10.33448/rsd-v11i6.28978
url https://rsdjournal.org/index.php/rsd/article/view/28978
identifier_str_mv 10.33448/rsd-v11i6.28978
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/28978/25168
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. 11 No. 6; e23911628978
Research, Society and Development; Vol. 11 Núm. 6; e23911628978
Research, Society and Development; v. 11 n. 6; e23911628978
2525-3409
reponame:Research, Society and Development
instname:Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
instname_str Universidade Federal de Itajubá (UNIFEI)
instacron_str UNIFEI
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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