VULVAR LICHEN SCLEROSUS – A REVIEW OF 208 CASES
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://doi.org/10.29021/spdv.70.1.41 |
Resumo: | Introduction: Lichen sclerosus (LS) is a chronic idiopathic inflammatory disease that preferentially affects the anogenital region and postmenopausal Caucasian women. Aims: Retrospective characterization of patients with vulvar LS diagnosed and treated at our Department (Vulvar Pathology Consultation), between 1986 and 2004. Material and Methods: A total of 208 Caucasians women were included in the study. We consulted clinical charts and performed statistical analysis of the following variables: age, location, clinical signs and symptoms, association with other disea- ses, treatment modalities, follow-up and complications. Results: The mean duration of LS was 6.3 years. The mean age at diagnosis was 59.6 years. The mean age at development of symptoms was 53 years. One hundred and eighty-two (87.5%) patients were in the postmenopausal period. Pruritus was the predominant symptom (90.9%). Only 39 (18.8%) patients did not developed vulvar atrophy. One hundred and forty-two (68.2%) had not narrowing of the vaginal in- troitus. Histological examination confirmed LS in 185 cases (93.9%) and it was compatible with LS in the remaining 12 (6.1%). Topical testosterone propionate (TP) was used in 88 (42.3%) cases, topical corticosteroids in 24 (11.5%) and both in 76 (36.6%). The mean follow-up was 9.5 years. Nine (4.3%) women developed vulvar SCC and the mean age at diagnosis was 68.2 years. Conclusions: LS prevailed in post-menopausal women. Vulvar pruritus and atrophy were the main clinical findings. Most cases were confirmed by histology. Topical TP was the most commonly used therapy. Malignancy occurred in nine cases.KEYWORDS – Vulvar Lichen Sclerosus; Testosterone Propionate; Glucocorticoids; Carcinoma, Squamous Cell. |
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VULVAR LICHEN SCLEROSUS – A REVIEW OF 208 CASESLÍQUEN ESCLEROSO DA VULVA – REVISÃO DE 208 CASOSIntroduction: Lichen sclerosus (LS) is a chronic idiopathic inflammatory disease that preferentially affects the anogenital region and postmenopausal Caucasian women. Aims: Retrospective characterization of patients with vulvar LS diagnosed and treated at our Department (Vulvar Pathology Consultation), between 1986 and 2004. Material and Methods: A total of 208 Caucasians women were included in the study. We consulted clinical charts and performed statistical analysis of the following variables: age, location, clinical signs and symptoms, association with other disea- ses, treatment modalities, follow-up and complications. Results: The mean duration of LS was 6.3 years. The mean age at diagnosis was 59.6 years. The mean age at development of symptoms was 53 years. One hundred and eighty-two (87.5%) patients were in the postmenopausal period. Pruritus was the predominant symptom (90.9%). Only 39 (18.8%) patients did not developed vulvar atrophy. One hundred and forty-two (68.2%) had not narrowing of the vaginal in- troitus. Histological examination confirmed LS in 185 cases (93.9%) and it was compatible with LS in the remaining 12 (6.1%). Topical testosterone propionate (TP) was used in 88 (42.3%) cases, topical corticosteroids in 24 (11.5%) and both in 76 (36.6%). The mean follow-up was 9.5 years. Nine (4.3%) women developed vulvar SCC and the mean age at diagnosis was 68.2 years. Conclusions: LS prevailed in post-menopausal women. Vulvar pruritus and atrophy were the main clinical findings. Most cases were confirmed by histology. Topical TP was the most commonly used therapy. Malignancy occurred in nine cases.KEYWORDS – Vulvar Lichen Sclerosus; Testosterone Propionate; Glucocorticoids; Carcinoma, Squamous Cell.Introdução: O líquen escleroso (LE) é uma dermatose inflamatória crónica idiopática com predilecção ano- genital, sendo mais comum na mulher no período pós-menopausa. Objectivos: Análise retrospectiva dos casos de LE vulvar diagnosticados e tratados na consulta de Patologia Vulvar, entre 1986 e 2004. Material e Métodos: Um total de 208 caucasianas foi incluído no estudo. Foram consultados processos clínicos e realizado estudo estatístico das variáveis idade, localização, sintomas e sinais clínicos, associação com outras patologias, tratamento, follow-up e complicações. Resultados: A duração média do LE foi de 6,3 anos. A idade média das mulheres à data do diagnóstico foi de 59,6 anos e à data do desenvolvimento dos sintomas de 53 anos. Cento e oitenta e duas (87,5%) encontravam-se no período pós-menopausa. O prurido foi o sintoma predominante (90,9%). Apenas 39 (18,8%) doentes não apresentavam atrofia vulvar e 142 (68,2%) não tinham envolvimento do intróito vaginal. O exame histológico confirmou LE em 185 (93,9%) e foi compatível nos restantes 12 (6,1%). O propionato de testosterona (PT) foi utilizado em 88 (42,3%) casos, os corticói- des tópicos em 24 (11,5%) e ambos em 76 (36,6%). O follow-up médio foi de 9,5 anos. Nove (4,3%) mulheres desenvol- veram CEC vulvar, sendo a idade média das mesmas ao diagnóstico de 68,2 anos. Conclusões: O LE predominou no período pós-menopausa. O prurido e atrofia vulvar foram os achados clínicos mais frequentes. A maior parte dos casos foi confirmado por histologia. O PT tópico foi a arma terapêutica mais usada. A malignização ocorreu em nove casos.PALAVRAS-CHAVE – Vulva; Líquen Escleroso; Propionato de Testosterona; Corticóides; Carcinoma Espinocelular.Sociedade Portuguesa de Dermatologia e Venereologia2013-01-20T00:00:00Zjournal articleinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://doi.org/10.29021/spdv.70.1.41oai:ojs.revista.spdv.com.pt:article/41Journal of the Portuguese Society of Dermatology and Venereology; Vol 70 No 1 (2012): Janeiro - Março; 81Revista da Sociedade Portuguesa de Dermatologia e Venereologia; v. 70 n. 1 (2012): Janeiro - Março; 812182-24092182-2395reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://revista.spdv.com.pt/index.php/spdv/article/view/41https://doi.org/10.29021/spdv.70.1.41https://revista.spdv.com.pt/index.php/spdv/article/view/41/42Torres, ErmelindoParente, JoanaAlmeida, J. C.Teixeira, JoséMartins, CésarAranha, Joãoinfo:eu-repo/semantics/openAccess2022-10-06T12:34:37Zoai:ojs.revista.spdv.com.pt:article/41Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:10:38.644049Repositório 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 |
VULVAR LICHEN SCLEROSUS – A REVIEW OF 208 CASES LÍQUEN ESCLEROSO DA VULVA – REVISÃO DE 208 CASOS |
title |
VULVAR LICHEN SCLEROSUS – A REVIEW OF 208 CASES |
spellingShingle |
VULVAR LICHEN SCLEROSUS – A REVIEW OF 208 CASES Torres, Ermelindo |
title_short |
VULVAR LICHEN SCLEROSUS – A REVIEW OF 208 CASES |
title_full |
VULVAR LICHEN SCLEROSUS – A REVIEW OF 208 CASES |
title_fullStr |
VULVAR LICHEN SCLEROSUS – A REVIEW OF 208 CASES |
title_full_unstemmed |
VULVAR LICHEN SCLEROSUS – A REVIEW OF 208 CASES |
title_sort |
VULVAR LICHEN SCLEROSUS – A REVIEW OF 208 CASES |
author |
Torres, Ermelindo |
author_facet |
Torres, Ermelindo Parente, Joana Almeida, J. C. Teixeira, José Martins, César Aranha, João |
author_role |
author |
author2 |
Parente, Joana Almeida, J. C. Teixeira, José Martins, César Aranha, João |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Torres, Ermelindo Parente, Joana Almeida, J. C. Teixeira, José Martins, César Aranha, João |
description |
Introduction: Lichen sclerosus (LS) is a chronic idiopathic inflammatory disease that preferentially affects the anogenital region and postmenopausal Caucasian women. Aims: Retrospective characterization of patients with vulvar LS diagnosed and treated at our Department (Vulvar Pathology Consultation), between 1986 and 2004. Material and Methods: A total of 208 Caucasians women were included in the study. We consulted clinical charts and performed statistical analysis of the following variables: age, location, clinical signs and symptoms, association with other disea- ses, treatment modalities, follow-up and complications. Results: The mean duration of LS was 6.3 years. The mean age at diagnosis was 59.6 years. The mean age at development of symptoms was 53 years. One hundred and eighty-two (87.5%) patients were in the postmenopausal period. Pruritus was the predominant symptom (90.9%). Only 39 (18.8%) patients did not developed vulvar atrophy. One hundred and forty-two (68.2%) had not narrowing of the vaginal in- troitus. Histological examination confirmed LS in 185 cases (93.9%) and it was compatible with LS in the remaining 12 (6.1%). Topical testosterone propionate (TP) was used in 88 (42.3%) cases, topical corticosteroids in 24 (11.5%) and both in 76 (36.6%). The mean follow-up was 9.5 years. Nine (4.3%) women developed vulvar SCC and the mean age at diagnosis was 68.2 years. Conclusions: LS prevailed in post-menopausal women. Vulvar pruritus and atrophy were the main clinical findings. Most cases were confirmed by histology. Topical TP was the most commonly used therapy. Malignancy occurred in nine cases.KEYWORDS – Vulvar Lichen Sclerosus; Testosterone Propionate; Glucocorticoids; Carcinoma, Squamous Cell. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-01-20T00:00:00Z |
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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.70.1.41 oai:ojs.revista.spdv.com.pt:article/41 |
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https://doi.org/10.29021/spdv.70.1.41 |
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oai:ojs.revista.spdv.com.pt:article/41 |
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por |
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https://revista.spdv.com.pt/index.php/spdv/article/view/41 https://doi.org/10.29021/spdv.70.1.41 https://revista.spdv.com.pt/index.php/spdv/article/view/41/42 |
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info:eu-repo/semantics/openAccess |
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Sociedade Portuguesa de Dermatologia e Venereologia |
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Sociedade Portuguesa de Dermatologia e Venereologia |
dc.source.none.fl_str_mv |
Journal of the Portuguese Society of Dermatology and Venereology; Vol 70 No 1 (2012): Janeiro - Março; 81 Revista da Sociedade Portuguesa de Dermatologia e Venereologia; v. 70 n. 1 (2012): Janeiro - Março; 81 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 |
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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) |
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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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