Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://doi.org/10.29021/spdv.76.1.835 |
Resumo: | Hidradenitis suppurativa (HS) is as a chronic, inflammatory and recurrent skin disease of the hair follicle. Prevalence of HS is a matter of debate, with estimate rates as low as 0.00033% and as high as 4.1%. HS prevalence appears significantly higher in women and has a mean age of onset in the early 20s. The primary histopathologic event seems to be a follicular hyperkeratosis with plugging, dilatation and rupture of the hair follicle resulting with subsequent inflammation and formation of abscesses and sinus tracts. The cause of this is likely multifactorial, involving genetic factors, cigarette smoking, mechanical stress, obesity, immune aberrant response and hormonal abnormalities. HS, as a chronic inflammatory dermatosis, is associated with a variety of concomitant and secondary diseases such as metabolic syndrome, inflammatory and rheumatologic diseases, depression and malignancy, and, for this reason HS management often requires a multidisciplinary team. |
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Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and ComorbiditiesAvanços na Hidradenite Supurativa: Da Etiopatogenia ao TratamentoHidradenitis suppurativaEpidemiologyPathogenesisQuality of life.Hidradenite Supurativa/diagnósticoHidradenite Supurativa/patologiaHidradenite Supurativa/tratamentoHidradenitis suppurativa (HS) is as a chronic, inflammatory and recurrent skin disease of the hair follicle. Prevalence of HS is a matter of debate, with estimate rates as low as 0.00033% and as high as 4.1%. HS prevalence appears significantly higher in women and has a mean age of onset in the early 20s. The primary histopathologic event seems to be a follicular hyperkeratosis with plugging, dilatation and rupture of the hair follicle resulting with subsequent inflammation and formation of abscesses and sinus tracts. The cause of this is likely multifactorial, involving genetic factors, cigarette smoking, mechanical stress, obesity, immune aberrant response and hormonal abnormalities. HS, as a chronic inflammatory dermatosis, is associated with a variety of concomitant and secondary diseases such as metabolic syndrome, inflammatory and rheumatologic diseases, depression and malignancy, and, for this reason HS management often requires a multidisciplinary team. A hidradenite supurativa é uma dermatose inflamatória crónica, recorrente, do folículo piloso. A prevalência de hidradenite supurativa é debatida, com taxas estimadas tão baixas como 0,00033% e tão altas como 4,1%. A prevalência da hidradenite supurativa parece ser significativamente maior nas mulheres. A sua etiopatogenia parece envolver hiperqueratose folicular com obstrução, dilatação e consequente rutura do folículo piloso, resultando em inflamação e formação subsequente de abcessos e trajetos sinuosos. A etiologia é provavelmente multifatorial, envolvendo fatores genéticos, tabagismo, stress mecânico, obesidade, resposta aberrante imune e anormalidades hormonais. A hidradenite supurativa, como dermatose inflamatória crónica, está associada a uma variedade de doenças concomitantes e secundárias, como síndrome metabólica, doenças inflamatórias e reumatológicas, depressão e neoplasias. Assim a abordagem da hidradenite supurativa requer uma equipa multidisciplinar.Sociedade Portuguesa de Dermatologia e Venereologia2018-04-05T00:00:00Zinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersionapplication/pdfimage/jpegimage/jpegimage/jpeghttps://doi.org/10.29021/spdv.76.1.835oai:ojs.revista.spdv.com.pt:article/835Journal of the Portuguese Society of Dermatology and Venereology; Vol 76 No 1 (2018): Janeiro - Março; 9-24Revista da Sociedade Portuguesa de Dermatologia e Venereologia; v. 76 n. 1 (2018): Janeiro - Março; 9-242182-24092182-2395reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttps://revista.spdv.com.pt/index.php/spdv/article/view/835https://doi.org/10.29021/spdv.76.1.835https://revista.spdv.com.pt/index.php/spdv/article/view/835/543https://revista.spdv.com.pt/index.php/spdv/article/view/835/744https://revista.spdv.com.pt/index.php/spdv/article/view/835/745https://revista.spdv.com.pt/index.php/spdv/article/view/835/746Costa e Silva, MiguelAzevedo, FilomenaLisboa, Carmeninfo:eu-repo/semantics/openAccess2022-10-06T12:35:05Zoai:ojs.revista.spdv.com.pt:article/835Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:11:04.520666Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities Avanços na Hidradenite Supurativa: Da Etiopatogenia ao Tratamento |
title |
Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities |
spellingShingle |
Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities Costa e Silva, Miguel Hidradenitis suppurativa Epidemiology Pathogenesis Quality of life. Hidradenite Supurativa/diagnóstico Hidradenite Supurativa/patologia Hidradenite Supurativa/tratamento |
title_short |
Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities |
title_full |
Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities |
title_fullStr |
Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities |
title_full_unstemmed |
Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities |
title_sort |
Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities |
author |
Costa e Silva, Miguel |
author_facet |
Costa e Silva, Miguel Azevedo, Filomena Lisboa, Carmen |
author_role |
author |
author2 |
Azevedo, Filomena Lisboa, Carmen |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Costa e Silva, Miguel Azevedo, Filomena Lisboa, Carmen |
dc.subject.por.fl_str_mv |
Hidradenitis suppurativa Epidemiology Pathogenesis Quality of life. Hidradenite Supurativa/diagnóstico Hidradenite Supurativa/patologia Hidradenite Supurativa/tratamento |
topic |
Hidradenitis suppurativa Epidemiology Pathogenesis Quality of life. Hidradenite Supurativa/diagnóstico Hidradenite Supurativa/patologia Hidradenite Supurativa/tratamento |
description |
Hidradenitis suppurativa (HS) is as a chronic, inflammatory and recurrent skin disease of the hair follicle. Prevalence of HS is a matter of debate, with estimate rates as low as 0.00033% and as high as 4.1%. HS prevalence appears significantly higher in women and has a mean age of onset in the early 20s. The primary histopathologic event seems to be a follicular hyperkeratosis with plugging, dilatation and rupture of the hair follicle resulting with subsequent inflammation and formation of abscesses and sinus tracts. The cause of this is likely multifactorial, involving genetic factors, cigarette smoking, mechanical stress, obesity, immune aberrant response and hormonal abnormalities. HS, as a chronic inflammatory dermatosis, is associated with a variety of concomitant and secondary diseases such as metabolic syndrome, inflammatory and rheumatologic diseases, depression and malignancy, and, for this reason HS management often requires a multidisciplinary team. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-04-05T00:00:00Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/other |
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info:eu-repo/semantics/publishedVersion |
format |
article |
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publishedVersion |
dc.identifier.uri.fl_str_mv |
https://doi.org/10.29021/spdv.76.1.835 oai:ojs.revista.spdv.com.pt:article/835 |
url |
https://doi.org/10.29021/spdv.76.1.835 |
identifier_str_mv |
oai:ojs.revista.spdv.com.pt:article/835 |
dc.language.iso.fl_str_mv |
eng |
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eng |
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https://revista.spdv.com.pt/index.php/spdv/article/view/835 https://doi.org/10.29021/spdv.76.1.835 https://revista.spdv.com.pt/index.php/spdv/article/view/835/543 https://revista.spdv.com.pt/index.php/spdv/article/view/835/744 https://revista.spdv.com.pt/index.php/spdv/article/view/835/745 https://revista.spdv.com.pt/index.php/spdv/article/view/835/746 |
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info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
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application/pdf image/jpeg image/jpeg image/jpeg |
dc.publisher.none.fl_str_mv |
Sociedade Portuguesa de Dermatologia e Venereologia |
publisher.none.fl_str_mv |
Sociedade Portuguesa de Dermatologia e Venereologia |
dc.source.none.fl_str_mv |
Journal of the Portuguese Society of Dermatology and Venereology; Vol 76 No 1 (2018): Janeiro - Março; 9-24 Revista da Sociedade Portuguesa de Dermatologia e Venereologia; v. 76 n. 1 (2018): Janeiro - Março; 9-24 2182-2409 2182-2395 reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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