Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities

Detalhes bibliográficos
Autor(a) principal: Costa e Silva, Miguel
Data de Publicação: 2018
Outros Autores: Azevedo, Filomena, Lisboa, Carmen
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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spelling 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
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dc.identifier.uri.fl_str_mv https://doi.org/10.29021/spdv.76.1.835
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url https://doi.org/10.29021/spdv.76.1.835
identifier_str_mv oai:ojs.revista.spdv.com.pt:article/835
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dc.relation.none.fl_str_mv 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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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
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