LICHEN PLANOPILARIS – A CASE ASSOCIATED WITH AUTOIMMUNE DISEASES
Main Author: | |
---|---|
Publication Date: | 2014 |
Other Authors: | , , |
Format: | Article |
Language: | por |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | https://doi.org/10.29021/spdv.72.3.286 |
Summary: | Due to the development of large areas of permanent alopecia, patients with lichen planopilaris are more likely to evolve with psychosocial disorders and lower quality of life. Lichen planopilaris (LPP) is characterized by an autoimmune response against antigens of the hair follicle. It is known that can coexist with systemic autoimmune diseases, although this relationship is not well understood. Early recognition and prompt therapy are to protect the base of the hair follicle and fibrosis can stop the progression of hair loss. We present a therapy used with excellent results in a case of lichen planus pillar overlap that occurred in dermatomyositis and scleroderma. |
id |
RCAP_f2c3537f45519b8c977c79f8ed33f76b |
---|---|
oai_identifier_str |
oai:ojs.revista.spdv.com.pt:article/286 |
network_acronym_str |
RCAP |
network_name_str |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
repository_id_str |
https://opendoar.ac.uk/repository/7160 |
spelling |
LICHEN PLANOPILARIS – A CASE ASSOCIATED WITH AUTOIMMUNE DISEASESLÍQUEN PLANO PILAR – RELATO DE UM CASO ASSOCIADO A DOENÇAS AUTOIMUNESAlopeciaLichen planusAlopeciaLíquen planoDue to the development of large areas of permanent alopecia, patients with lichen planopilaris are more likely to evolve with psychosocial disorders and lower quality of life. Lichen planopilaris (LPP) is characterized by an autoimmune response against antigens of the hair follicle. It is known that can coexist with systemic autoimmune diseases, although this relationship is not well understood. Early recognition and prompt therapy are to protect the base of the hair follicle and fibrosis can stop the progression of hair loss. We present a therapy used with excellent results in a case of lichen planus pillar overlap that occurred in dermatomyositis and scleroderma.Devido ao desenvolvimento de grandes áreas permanentes de alopecia, os pacientes com LPP são mais propensos a evoluir com distúrbios psicossociais e menor qualidade de vida. O líquen plano pilar (LPP) é caracterizado por uma resposta autoimune contra antígenos do folículo piloso. Sabe-se que pode coexistir com doenças imunológicas sistêmicas, porém essa relação ainda não é bem compreendida. O reconhecimento precoce e a terapia imediata são a base para proteger o folículo piloso de possível fibrose e deter a progressão da perda capilar. Apresentamos uma terapêutica com excelente resultado utilizada em um caso de líquen plano pilar que ocorreu em overlap a dermatomiosite e esclerodermia.Sociedade Portuguesa de Dermatologia e Venereologia2014-10-12T00:00:00Zjournal articleinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://doi.org/10.29021/spdv.72.3.286oai:ojs.revista.spdv.com.pt:article/286Journal of the Portuguese Society of Dermatology and Venereology; Vol 72 No 3 (2014): Julho - Setembro; 395-399Revista da Sociedade Portuguesa de Dermatologia e Venereologia; v. 72 n. 3 (2014): Julho - Setembro; 395-3992182-24092182-2395reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAPporhttps://revista.spdv.com.pt/index.php/spdv/article/view/286https://doi.org/10.29021/spdv.72.3.286https://revista.spdv.com.pt/index.php/spdv/article/view/286/281Ramos, Luana OliveiraKlein, Ana Paulados Santos, Ana Paula Gualda Botelhodo Valle, Fábio Francesconiinfo:eu-repo/semantics/openAccess2022-10-06T12:34:49Zoai:ojs.revista.spdv.com.pt:article/286Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T10:31:02.358022Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
LICHEN PLANOPILARIS – A CASE ASSOCIATED WITH AUTOIMMUNE DISEASES LÍQUEN PLANO PILAR – RELATO DE UM CASO ASSOCIADO A DOENÇAS AUTOIMUNES |
title |
LICHEN PLANOPILARIS – A CASE ASSOCIATED WITH AUTOIMMUNE DISEASES |
spellingShingle |
LICHEN PLANOPILARIS – A CASE ASSOCIATED WITH AUTOIMMUNE DISEASES Ramos, Luana Oliveira Alopecia Lichen planus Alopecia Líquen plano |
title_short |
LICHEN PLANOPILARIS – A CASE ASSOCIATED WITH AUTOIMMUNE DISEASES |
title_full |
LICHEN PLANOPILARIS – A CASE ASSOCIATED WITH AUTOIMMUNE DISEASES |
title_fullStr |
LICHEN PLANOPILARIS – A CASE ASSOCIATED WITH AUTOIMMUNE DISEASES |
title_full_unstemmed |
LICHEN PLANOPILARIS – A CASE ASSOCIATED WITH AUTOIMMUNE DISEASES |
title_sort |
LICHEN PLANOPILARIS – A CASE ASSOCIATED WITH AUTOIMMUNE DISEASES |
author |
Ramos, Luana Oliveira |
author_facet |
Ramos, Luana Oliveira Klein, Ana Paula dos Santos, Ana Paula Gualda Botelho do Valle, Fábio Francesconi |
author_role |
author |
author2 |
Klein, Ana Paula dos Santos, Ana Paula Gualda Botelho do Valle, Fábio Francesconi |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Ramos, Luana Oliveira Klein, Ana Paula dos Santos, Ana Paula Gualda Botelho do Valle, Fábio Francesconi |
dc.subject.por.fl_str_mv |
Alopecia Lichen planus Alopecia Líquen plano |
topic |
Alopecia Lichen planus Alopecia Líquen plano |
description |
Due to the development of large areas of permanent alopecia, patients with lichen planopilaris are more likely to evolve with psychosocial disorders and lower quality of life. Lichen planopilaris (LPP) is characterized by an autoimmune response against antigens of the hair follicle. It is known that can coexist with systemic autoimmune diseases, although this relationship is not well understood. Early recognition and prompt therapy are to protect the base of the hair follicle and fibrosis can stop the progression of hair loss. We present a therapy used with excellent results in a case of lichen planus pillar overlap that occurred in dermatomyositis and scleroderma. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-10-12T00:00:00Z |
dc.type.driver.fl_str_mv |
journal article info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://doi.org/10.29021/spdv.72.3.286 oai:ojs.revista.spdv.com.pt:article/286 |
url |
https://doi.org/10.29021/spdv.72.3.286 |
identifier_str_mv |
oai:ojs.revista.spdv.com.pt:article/286 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://revista.spdv.com.pt/index.php/spdv/article/view/286 https://doi.org/10.29021/spdv.72.3.286 https://revista.spdv.com.pt/index.php/spdv/article/view/286/281 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
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 72 No 3 (2014): Julho - Setembro; 395-399 Revista da Sociedade Portuguesa de Dermatologia e Venereologia; v. 72 n. 3 (2014): Julho - Setembro; 395-399 2182-2409 2182-2395 reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia instacron:RCAAP |
instname_str |
FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
collection |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
repository.name.fl_str_mv |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
repository.mail.fl_str_mv |
info@rcaap.pt |
_version_ |
1833590934169714688 |