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Polymorphous low-grade adenocarcinoma: an analysis of epidemiological studies and hints for pathologists

BACKGROUND: This study is an analysis of the prevalence of polymorphous low grade adenocarcinoma (PLGA) in epidemiological surveys of salivary tumors published in the English language from 1992 to 2012. METHODS: These surveys included studies from different researchers, countries and continents. The...

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Autores principales: de Araujo, Vera Cavalcanti, Passador-Santos, Fabricio, Turssi, Cecilia, Soares, Andresa Borges, de Araujo, Ney Soares
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3564831/
https://www.ncbi.nlm.nih.gov/pubmed/23320410
http://dx.doi.org/10.1186/1746-1596-8-6
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author de Araujo, Vera Cavalcanti
Passador-Santos, Fabricio
Turssi, Cecilia
Soares, Andresa Borges
de Araujo, Ney Soares
author_facet de Araujo, Vera Cavalcanti
Passador-Santos, Fabricio
Turssi, Cecilia
Soares, Andresa Borges
de Araujo, Ney Soares
author_sort de Araujo, Vera Cavalcanti
collection PubMed
description BACKGROUND: This study is an analysis of the prevalence of polymorphous low grade adenocarcinoma (PLGA) in epidemiological surveys of salivary tumors published in the English language from 1992 to 2012. METHODS: These surveys included studies from different researchers, countries and continents. The 57 surveys for which it was possible to calculate the percentage of PLGAs among all malignant minor salivary gland tumors (MMSGT) were included in this review. RESULTS: The statistical analyses show significant differences in the PLGA percentage by time period, country and continent in the studies included in this review. The percentage of PLGAs among MMSGTs varied among the studies, ranging from 0.0% to 46.8%. PLGA rates have varied over the period studied and have most recently increased. The frequency of reported PLGA cases also varied from 0.0% to 24.8% by the country in which the MMSGT studies were performed. The PLGA percentages also varied significantly by continent, with frequencies ranging from 3.9% in Asia to 20.0% in Oceania CONCLUSION: Based on these results, we concluded that although the accuracy of PLGA diagnoses has improved, they remain a challenge for pathologists. To facilitate PLGA diagnoses, we have therefore made some suggestions for pathologists regarding tumors composed of single-layer strands of cells that form all of the histological patterns present in the tumor, consistency of the cytological appearance and uniformly positive CK7, vimentin and S100 immunohistochemistry, which indicate a single PLGA phenotype. VIRTUAL SLIDE: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1059098656858324
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spelling pubmed-35648312013-02-08 Polymorphous low-grade adenocarcinoma: an analysis of epidemiological studies and hints for pathologists de Araujo, Vera Cavalcanti Passador-Santos, Fabricio Turssi, Cecilia Soares, Andresa Borges de Araujo, Ney Soares Diagn Pathol Research BACKGROUND: This study is an analysis of the prevalence of polymorphous low grade adenocarcinoma (PLGA) in epidemiological surveys of salivary tumors published in the English language from 1992 to 2012. METHODS: These surveys included studies from different researchers, countries and continents. The 57 surveys for which it was possible to calculate the percentage of PLGAs among all malignant minor salivary gland tumors (MMSGT) were included in this review. RESULTS: The statistical analyses show significant differences in the PLGA percentage by time period, country and continent in the studies included in this review. The percentage of PLGAs among MMSGTs varied among the studies, ranging from 0.0% to 46.8%. PLGA rates have varied over the period studied and have most recently increased. The frequency of reported PLGA cases also varied from 0.0% to 24.8% by the country in which the MMSGT studies were performed. The PLGA percentages also varied significantly by continent, with frequencies ranging from 3.9% in Asia to 20.0% in Oceania CONCLUSION: Based on these results, we concluded that although the accuracy of PLGA diagnoses has improved, they remain a challenge for pathologists. To facilitate PLGA diagnoses, we have therefore made some suggestions for pathologists regarding tumors composed of single-layer strands of cells that form all of the histological patterns present in the tumor, consistency of the cytological appearance and uniformly positive CK7, vimentin and S100 immunohistochemistry, which indicate a single PLGA phenotype. VIRTUAL SLIDE: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1059098656858324 BioMed Central 2013-01-15 /pmc/articles/PMC3564831/ /pubmed/23320410 http://dx.doi.org/10.1186/1746-1596-8-6 Text en Copyright ©2013 de Araujo et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
de Araujo, Vera Cavalcanti
Passador-Santos, Fabricio
Turssi, Cecilia
Soares, Andresa Borges
de Araujo, Ney Soares
Polymorphous low-grade adenocarcinoma: an analysis of epidemiological studies and hints for pathologists
title Polymorphous low-grade adenocarcinoma: an analysis of epidemiological studies and hints for pathologists
title_full Polymorphous low-grade adenocarcinoma: an analysis of epidemiological studies and hints for pathologists
title_fullStr Polymorphous low-grade adenocarcinoma: an analysis of epidemiological studies and hints for pathologists
title_full_unstemmed Polymorphous low-grade adenocarcinoma: an analysis of epidemiological studies and hints for pathologists
title_short Polymorphous low-grade adenocarcinoma: an analysis of epidemiological studies and hints for pathologists
title_sort polymorphous low-grade adenocarcinoma: an analysis of epidemiological studies and hints for pathologists
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3564831/
https://www.ncbi.nlm.nih.gov/pubmed/23320410
http://dx.doi.org/10.1186/1746-1596-8-6
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