Sweet's Syndrome: case report of a rare occurrence
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , |
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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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 |
_version_ |
1797052819488899072 |