Sweet's Syndrome: case report of a rare occurrence

Detalhes bibliográficos
Autor(a) principal: Leite, Cleber Queiroz
Data de Publicação: 2021
Outros Autores: Santos, Brian França dos, Silva, Messias Genézio Santana da, Borges, Stefany Ohana Oliveira Costa
Tipo de documento: Artigo
Idioma: por
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/22925
Resumo: Sweet's syndrome (SS) is a rare systemic inflammatory condition, which is characterized by the sudden appearance of erythemoedematous cutaneous plaques and nodules, related to systemic symptoms and infiltration of mature neutrophils in histopathological studies. Currently, the disease is classified into three categories: classic (idiopathic), associated with malignancy and drug-induced, and the classic constitutes the majority of cases. In this context, we present a case of a 72-year-old man with a typical picture of the classic form of Sweet's Syndrome, where he presented regression of the lesions after 2 weeks of treatment, and in these cases the regression starts 72 hours after the start of corticosteroid therapy. systemic. Despite Sweet's Syndrome being a rare disease, with the diagnosis and proper therapeutic establishment and with the use of systemic corticotherapy, the results end up being extremely fast and favorable to its patients. Therefore, the diagnosis and classification of the form of Sweet's Syndrome provides an adequate therapeutic direction, considering that in cases in which they are induced by drugs or associated with cancer, there are only satisfactory and lasting therapeutic responses, when the treatment is carried out. of the underlying disease and discontinuation of the causative drug, respectively.
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spelling Sweet's Syndrome: case report of a rare occurrenceSíndrome de Sweet: reporte de caso de uma ocurrencia raraSíndrome de Sweet: relato de caso de um acontecimento raroSíndrome de SweetCorticoideDermatose Neutrofílica Aguda FebrilInfiltração de neutrófilos.Síndrome de SweetCorticosteroidesDermatosis neutrofílica aguda febrilInfiltración de neutrófilos.Sweet's SyndromeCorticosteroidsFebrile Acute Neutrophilic DermatosisNeutrophil infiltration.Sweet's syndrome (SS) is a rare systemic inflammatory condition, which is characterized by the sudden appearance of erythemoedematous cutaneous plaques and nodules, related to systemic symptoms and infiltration of mature neutrophils in histopathological studies. Currently, the disease is classified into three categories: classic (idiopathic), associated with malignancy and drug-induced, and the classic constitutes the majority of cases. In this context, we present a case of a 72-year-old man with a typical picture of the classic form of Sweet's Syndrome, where he presented regression of the lesions after 2 weeks of treatment, and in these cases the regression starts 72 hours after the start of corticosteroid therapy. systemic. Despite Sweet's Syndrome being a rare disease, with the diagnosis and proper therapeutic establishment and with the use of systemic corticotherapy, the results end up being extremely fast and favorable to its patients. Therefore, the diagnosis and classification of the form of Sweet's Syndrome provides an adequate therapeutic direction, considering that in cases in which they are induced by drugs or associated with cancer, there are only satisfactory and lasting therapeutic responses, when the treatment is carried out. of the underlying disease and discontinuation of the causative drug, respectively.El síndrome de Sweet (SS) es una enfermedad inflamatoria sistémica poco frecuente, que se caracteriza por la aparición repentina de placas y nódulos cutáneos eritemoedematosos, relacionados con síntomas sistémicos e infiltración de neutrófilos maduros en estudios histopatológicos. Actualmente, la enfermedad se clasifica en tres categorías: clásica (idiopática), asociada a malignidad e inducida por fármacos, y la clásica constituye la mayoría de los casos. En este contexto, presentamos el caso de un hombre de 72 años con un cuadro típico de la forma clásica del Síndrome de Sweet, donde presentó regresión de las lesiones a las 2 semanas de tratamiento, y en estos casos la regresión comienza a las 72 horas. después del inicio de la terapia con corticosteroides sistémicos. A pesar de que el Síndrome de Sweet es una enfermedad rara, con el diagnóstico y establecimiento terapéutico adecuado y con el uso de corticoterapia sistémica, los resultados terminan siendo sumamente rápidos y favorables para sus pacientes. Por tanto, el diagnóstico y clasificación de la forma del Síndrome de Sweet proporciona una adecuada orientación terapéutica, considerando que en los casos en que son inducidos por fármacos o asociados a neoplasias, solo existen respuestas terapéuticas satisfactorias y duraderas, cuando se realiza el tratamiento. de la enfermedad subyacente y la interrupción del fármaco causante, respectivamente.A síndrome de Sweet (SS) e uma condição inflamatória sistêmica rara, que se caracteriza-se pelo aparecimento súbito de placas e nódulos cutâneos eritêmo-edematoso, relacionados a sintomas sistêmicos e a infiltração de neutrófilos maduros a estudos histopatológicos. Atualmente a doença é classificada em três categorias: clássica (idiopática), associada à malignidade e induzida por drogas, sendo que a clássica constitui a maioria dos casos. Nesse contexto, apresentamos um caso de um homem de 72 anos com quadro típico da forma clássica de Síndrome de Sweet, onde apresentou regressão das lesões após 2 semanas de tratamento, sendo que nesses casos a regressão inicia-se 72 horas após o início da corticoterapia sistêmica. Apesar da Síndrome de Sweet ser uma doença rara, com o diagnóstico e a instauração terapêutica adequada e com a utilização da corticoterapia sistêmica, os resultados acabam sendo extremamente rápidos e favoráveis aos seus portadores. Assim sendo, o diagnóstico e a classificação da forma da Síndrome de Sweet concede um direcionamento terapêutico adequado, tendo em vista que nos casos em que são induzidos por drogas ou associados a neoplasias, só existem respostas terapêuticas satisfatórias e duradouras, quando se realiza o tratamento da doença de base e a suspensão da droga causadora, respectivamente.Research, Society and Development2021-11-24info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/2292510.33448/rsd-v10i15.22925Research, Society and Development; Vol. 10 No. 15; e181101522925Research, Society and Development; Vol. 10 Núm. 15; e181101522925Research, Society and Development; v. 10 n. 15; e1811015229252525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/22925/20223Copyright (c) 2021 Cleber Queiroz Leite; Brian França dos Santos; Messias Genézio Santana da Silva; Stefany Ohana Oliveira Costa Borgeshttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessLeite, Cleber Queiroz Santos, Brian França dos Silva, Messias Genézio Santana da Borges, Stefany Ohana Oliveira Costa2021-12-06T10:13:53Zoai:ojs.pkp.sfu.ca:article/22925Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:41:56.951160Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Sweet's Syndrome: case report of a rare occurrence
Síndrome de Sweet: reporte de caso de uma ocurrencia rara
Síndrome de Sweet: relato de caso de um acontecimento raro
title Sweet's Syndrome: case report of a rare occurrence
spellingShingle Sweet's Syndrome: case report of a rare occurrence
Leite, Cleber Queiroz
Síndrome de Sweet
Corticoide
Dermatose Neutrofílica Aguda Febril
Infiltração de neutrófilos.
Síndrome de Sweet
Corticosteroides
Dermatosis neutrofílica aguda febril
Infiltración de neutrófilos.
Sweet's Syndrome
Corticosteroids
Febrile Acute Neutrophilic Dermatosis
Neutrophil infiltration.
title_short Sweet's Syndrome: case report of a rare occurrence
title_full Sweet's Syndrome: case report of a rare occurrence
title_fullStr Sweet's Syndrome: case report of a rare occurrence
title_full_unstemmed Sweet's Syndrome: case report of a rare occurrence
title_sort Sweet's Syndrome: case report of a rare occurrence
author Leite, Cleber Queiroz
author_facet Leite, Cleber Queiroz
Santos, Brian França dos
Silva, Messias Genézio Santana da
Borges, Stefany Ohana Oliveira Costa
author_role author
author2 Santos, Brian França dos
Silva, Messias Genézio Santana da
Borges, Stefany Ohana Oliveira Costa
author2_role author
author
author
dc.contributor.author.fl_str_mv Leite, Cleber Queiroz
Santos, Brian França dos
Silva, Messias Genézio Santana da
Borges, Stefany Ohana Oliveira Costa
dc.subject.por.fl_str_mv Síndrome de Sweet
Corticoide
Dermatose Neutrofílica Aguda Febril
Infiltração de neutrófilos.
Síndrome de Sweet
Corticosteroides
Dermatosis neutrofílica aguda febril
Infiltración de neutrófilos.
Sweet's Syndrome
Corticosteroids
Febrile Acute Neutrophilic Dermatosis
Neutrophil infiltration.
topic Síndrome de Sweet
Corticoide
Dermatose Neutrofílica Aguda Febril
Infiltração de neutrófilos.
Síndrome de Sweet
Corticosteroides
Dermatosis neutrofílica aguda febril
Infiltración de neutrófilos.
Sweet's Syndrome
Corticosteroids
Febrile Acute Neutrophilic Dermatosis
Neutrophil infiltration.
description Sweet's syndrome (SS) is a rare systemic inflammatory condition, which is characterized by the sudden appearance of erythemoedematous cutaneous plaques and nodules, related to systemic symptoms and infiltration of mature neutrophils in histopathological studies. Currently, the disease is classified into three categories: classic (idiopathic), associated with malignancy and drug-induced, and the classic constitutes the majority of cases. In this context, we present a case of a 72-year-old man with a typical picture of the classic form of Sweet's Syndrome, where he presented regression of the lesions after 2 weeks of treatment, and in these cases the regression starts 72 hours after the start of corticosteroid therapy. systemic. Despite Sweet's Syndrome being a rare disease, with the diagnosis and proper therapeutic establishment and with the use of systemic corticotherapy, the results end up being extremely fast and favorable to its patients. Therefore, the diagnosis and classification of the form of Sweet's Syndrome provides an adequate therapeutic direction, considering that in cases in which they are induced by drugs or associated with cancer, there are only satisfactory and lasting therapeutic responses, when the treatment is carried out. of the underlying disease and discontinuation of the causative drug, respectively.
publishDate 2021
dc.date.none.fl_str_mv 2021-11-24
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/22925
10.33448/rsd-v10i15.22925
url https://rsdjournal.org/index.php/rsd/article/view/22925
identifier_str_mv 10.33448/rsd-v10i15.22925
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/22925/20223
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. 15; e181101522925
Research, Society and Development; Vol. 10 Núm. 15; e181101522925
Research, Society and Development; v. 10 n. 15; e181101522925
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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