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Clinicopathological Proficiency in the Diagnosis of Kaposi's Sarcoma

Background. The prevalence of Kaposi's sarcoma (KS), an AIDS-defining illness, has increased in parallel with the HIV/AIDS epidemic. The presence of violaceous skin lesions should raise suspicion of KS. However, especially on dark skin, KS mimics a variety of non-KS skin conditions. Histologica...

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Autor principal: van Bogaert, Louis-Jacques
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scholarly Research Network 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765762/
https://www.ncbi.nlm.nih.gov/pubmed/24052878
http://dx.doi.org/10.5402/2012/565463
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author van Bogaert, Louis-Jacques
author_facet van Bogaert, Louis-Jacques
author_sort van Bogaert, Louis-Jacques
collection PubMed
description Background. The prevalence of Kaposi's sarcoma (KS), an AIDS-defining illness, has increased in parallel with the HIV/AIDS epidemic. The presence of violaceous skin lesions should raise suspicion of KS. However, especially on dark skin, KS mimics a variety of non-KS skin conditions. Histologically, there is a wide range of expressions of KS and a large number of mimickers. For all these reasons, a HHV-8 immunohistochemically biopsy-proven diagnosis of KS should be the gold standard. Methods. Prospective study of 490 consecutive skin biopsies from the general community in the Limpopo Province of South Africa, from April 2010 through December 2011. Results. The clinical discordance rate (over-/underdiagnosis of KS) was 30.5%; the histological discordance rate was 9.2%. Conclusion. Because of the magnitude of diagnostic error, both clinical and histological, all clinical lesions suspicious of KS should be biopsied and HHV-8 LAN-1 immunophenotyped.
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spelling pubmed-37657622013-09-19 Clinicopathological Proficiency in the Diagnosis of Kaposi's Sarcoma van Bogaert, Louis-Jacques ISRN AIDS Clinical Study Background. The prevalence of Kaposi's sarcoma (KS), an AIDS-defining illness, has increased in parallel with the HIV/AIDS epidemic. The presence of violaceous skin lesions should raise suspicion of KS. However, especially on dark skin, KS mimics a variety of non-KS skin conditions. Histologically, there is a wide range of expressions of KS and a large number of mimickers. For all these reasons, a HHV-8 immunohistochemically biopsy-proven diagnosis of KS should be the gold standard. Methods. Prospective study of 490 consecutive skin biopsies from the general community in the Limpopo Province of South Africa, from April 2010 through December 2011. Results. The clinical discordance rate (over-/underdiagnosis of KS) was 30.5%; the histological discordance rate was 9.2%. Conclusion. Because of the magnitude of diagnostic error, both clinical and histological, all clinical lesions suspicious of KS should be biopsied and HHV-8 LAN-1 immunophenotyped. International Scholarly Research Network 2012-05-30 /pmc/articles/PMC3765762/ /pubmed/24052878 http://dx.doi.org/10.5402/2012/565463 Text en Copyright © 2012 Louis-Jacques van Bogaert. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
van Bogaert, Louis-Jacques
Clinicopathological Proficiency in the Diagnosis of Kaposi's Sarcoma
title Clinicopathological Proficiency in the Diagnosis of Kaposi's Sarcoma
title_full Clinicopathological Proficiency in the Diagnosis of Kaposi's Sarcoma
title_fullStr Clinicopathological Proficiency in the Diagnosis of Kaposi's Sarcoma
title_full_unstemmed Clinicopathological Proficiency in the Diagnosis of Kaposi's Sarcoma
title_short Clinicopathological Proficiency in the Diagnosis of Kaposi's Sarcoma
title_sort clinicopathological proficiency in the diagnosis of kaposi's sarcoma
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765762/
https://www.ncbi.nlm.nih.gov/pubmed/24052878
http://dx.doi.org/10.5402/2012/565463
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