KAPOSI´S SARCOMA - A CLINICOPATHOLOGICAL REVIEW
Autor(a) principal: | |
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Data de Publicação: | 2015 |
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.72.4.316 |
Resumo: | Introduction: Kaposi's sarcoma (KS) is a systemic disease, whose neoplastic or reactive nature is controversial and its etiologic agent is human herpes virus type 8 (HHV-8). There are 4 clinical subtypes: classical, epidemic, endemic and iatrogenic.Material and methods: A retrospective review of clinical records and histological preparations of KS cases, diagnosed between January 2001 and December 2013 at the Dermatopathology Department of Hospital Egas Moniz and Centro de Dermatologia Médico-Cirúrgica de Lisboa was made and we assessed differences between the various types.Results: Ninety-one cases were diagnosed, 67.0% of classic KS, 30.8% of epidemic KS; 1.1% of endemic KS and 1.1% of iatrogenic KS. It was found that 85.7% of patients were male and 14.3% were female, and this dominance occurred in all variants. The average age of patients with epidemic KS was lower than the classic variant (37.3 vs 70.0 years, p< 0.001). The lower limbs were the preferred location for all variants (74.2%). Histologically, in patients with classic KS, there was a predominance of the nodule stage (62.3%), while in epidemic KS, plaque was the most common stage (46.4 %) and this difference being almost statistically significant ( p = 0.057). No differences were observed in the various histological stages between classic and epidemic SK.Conclusions: The observed differences in epidemic KS seem to relate more with subtle changes inherent to early lesions rather than only differences of this variant , which is in agreement with the literature. |
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KAPOSI´S SARCOMA - A CLINICOPATHOLOGICAL REVIEWSARCOMA DE KAPOSI - REVISÃO CLÍNICO-PATOLÓGICASarcomaKaposiclassificationanatomy and histologySarcoma de KaposiclassificaçãohistologiaIntroduction: Kaposi's sarcoma (KS) is a systemic disease, whose neoplastic or reactive nature is controversial and its etiologic agent is human herpes virus type 8 (HHV-8). There are 4 clinical subtypes: classical, epidemic, endemic and iatrogenic.Material and methods: A retrospective review of clinical records and histological preparations of KS cases, diagnosed between January 2001 and December 2013 at the Dermatopathology Department of Hospital Egas Moniz and Centro de Dermatologia Médico-Cirúrgica de Lisboa was made and we assessed differences between the various types.Results: Ninety-one cases were diagnosed, 67.0% of classic KS, 30.8% of epidemic KS; 1.1% of endemic KS and 1.1% of iatrogenic KS. It was found that 85.7% of patients were male and 14.3% were female, and this dominance occurred in all variants. The average age of patients with epidemic KS was lower than the classic variant (37.3 vs 70.0 years, p< 0.001). The lower limbs were the preferred location for all variants (74.2%). Histologically, in patients with classic KS, there was a predominance of the nodule stage (62.3%), while in epidemic KS, plaque was the most common stage (46.4 %) and this difference being almost statistically significant ( p = 0.057). No differences were observed in the various histological stages between classic and epidemic SK.Conclusions: The observed differences in epidemic KS seem to relate more with subtle changes inherent to early lesions rather than only differences of this variant , which is in agreement with the literature.Introdução: O Sarcoma de Kaposi (SK) é uma afecção sistémica, cuja natureza neoplásica ou reactiva é controversa, que parece ter como origem a célula endotelial linfática e tem como agente etiológico o vírus herpes humano tipo 8 (HHV8). Existem 4 subtipos clínicos: clássico, epidémico, endémico e iatrogénico.Objectivos, material e métodos: Revisão retrospectiva dos processos clínicos e preparações histológicas dos casos de SK diagnosticados entre Janeiro de 2001 e Dezembro de 2013, nos departamentos de Dermatopatologia do Hospital Egas Moniz e Centro de Dermatologia Médico-Cirúrgica de Lisboa e avaliar diferenças entre os vários tipos.Resultados: Incluiu-se um total de 91 doentes, dos quais 67,0% correspondiam a SK clássico; 30,8% a SK epidémico; 1,1% a SK endémico e 1,1% a SK iatrogénico. Verificou-se que 85,7% dos doentes eram do sexo masculino e 14,3% do sexo feminino, sendo que este predomínio ocorreu em todas as variantes. A média de idades dos doentes com SK epidémico foi inferior ao SK clássico (37,3 vs 70,0 anos, p<0.001). Os membros inferiores foram a localização preferencial de todas as variantes (74,2%). Histologicamente, nos doentes com SK clássico, verificou-se um predomínio do estádio nódulo (62,3%), enquanto no SK epidémico o estádio mais comum foi placa (46,4%), sendo esta diferença quase estatisticamente significativa (p= 0,057). Não se observaram diferenças nos vários estádios histológicos nos diferentes subtipos clínicos.Conclusões: As diferenças observadas no SK epidémico parecem relacionar-se mais com alterações subtis, inerentes a lesões precoces, em vez de diferenças únicas desta variante, o que está de acordo com a literatura.Sociedade Portuguesa de Dermatologia e Venereologia2015-04-13T00:00:00Zjournal articleinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://doi.org/10.29021/spdv.72.4.316oai:ojs.revista.spdv.com.pt:article/316Journal of the Portuguese Society of Dermatology and Venereology; Vol 72 No 4 (2014): Outubro - Dezembro; 471-478Revista da Sociedade Portuguesa de Dermatologia e Venereologia; v. 72 n. 4 (2014): Outubro - Dezembro; 471-4782182-24092182-2395reponame: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/316https://doi.org/10.29021/spdv.72.4.316https://revista.spdv.com.pt/index.php/spdv/article/view/316/290Resende, CristinaAzevedo, T.Henriques, A.Calima, Z.Oliveira, P.Vale, E.Viana, I.info:eu-repo/semantics/openAccess2022-10-06T12:34:50Zoai:ojs.revista.spdv.com.pt:article/316Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:10:49.992800Repositório 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 |
KAPOSI´S SARCOMA - A CLINICOPATHOLOGICAL REVIEW SARCOMA DE KAPOSI - REVISÃO CLÍNICO-PATOLÓGICA |
title |
KAPOSI´S SARCOMA - A CLINICOPATHOLOGICAL REVIEW |
spellingShingle |
KAPOSI´S SARCOMA - A CLINICOPATHOLOGICAL REVIEW Resende, Cristina Sarcoma Kaposi classification anatomy and histology Sarcoma de Kaposi classificação histologia |
title_short |
KAPOSI´S SARCOMA - A CLINICOPATHOLOGICAL REVIEW |
title_full |
KAPOSI´S SARCOMA - A CLINICOPATHOLOGICAL REVIEW |
title_fullStr |
KAPOSI´S SARCOMA - A CLINICOPATHOLOGICAL REVIEW |
title_full_unstemmed |
KAPOSI´S SARCOMA - A CLINICOPATHOLOGICAL REVIEW |
title_sort |
KAPOSI´S SARCOMA - A CLINICOPATHOLOGICAL REVIEW |
author |
Resende, Cristina |
author_facet |
Resende, Cristina Azevedo, T. Henriques, A. Calima, Z. Oliveira, P. Vale, E. Viana, I. |
author_role |
author |
author2 |
Azevedo, T. Henriques, A. Calima, Z. Oliveira, P. Vale, E. Viana, I. |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Resende, Cristina Azevedo, T. Henriques, A. Calima, Z. Oliveira, P. Vale, E. Viana, I. |
dc.subject.por.fl_str_mv |
Sarcoma Kaposi classification anatomy and histology Sarcoma de Kaposi classificação histologia |
topic |
Sarcoma Kaposi classification anatomy and histology Sarcoma de Kaposi classificação histologia |
description |
Introduction: Kaposi's sarcoma (KS) is a systemic disease, whose neoplastic or reactive nature is controversial and its etiologic agent is human herpes virus type 8 (HHV-8). There are 4 clinical subtypes: classical, epidemic, endemic and iatrogenic.Material and methods: A retrospective review of clinical records and histological preparations of KS cases, diagnosed between January 2001 and December 2013 at the Dermatopathology Department of Hospital Egas Moniz and Centro de Dermatologia Médico-Cirúrgica de Lisboa was made and we assessed differences between the various types.Results: Ninety-one cases were diagnosed, 67.0% of classic KS, 30.8% of epidemic KS; 1.1% of endemic KS and 1.1% of iatrogenic KS. It was found that 85.7% of patients were male and 14.3% were female, and this dominance occurred in all variants. The average age of patients with epidemic KS was lower than the classic variant (37.3 vs 70.0 years, p< 0.001). The lower limbs were the preferred location for all variants (74.2%). Histologically, in patients with classic KS, there was a predominance of the nodule stage (62.3%), while in epidemic KS, plaque was the most common stage (46.4 %) and this difference being almost statistically significant ( p = 0.057). No differences were observed in the various histological stages between classic and epidemic SK.Conclusions: The observed differences in epidemic KS seem to relate more with subtle changes inherent to early lesions rather than only differences of this variant , which is in agreement with the literature. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-04-13T00:00:00Z |
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.72.4.316 oai:ojs.revista.spdv.com.pt:article/316 |
url |
https://doi.org/10.29021/spdv.72.4.316 |
identifier_str_mv |
oai:ojs.revista.spdv.com.pt:article/316 |
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por |
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dc.relation.none.fl_str_mv |
https://revista.spdv.com.pt/index.php/spdv/article/view/316 https://doi.org/10.29021/spdv.72.4.316 https://revista.spdv.com.pt/index.php/spdv/article/view/316/290 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
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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 72 No 4 (2014): Outubro - Dezembro; 471-478 Revista da Sociedade Portuguesa de Dermatologia e Venereologia; v. 72 n. 4 (2014): Outubro - Dezembro; 471-478 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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