Mammaglobin and DOG‐1 expression in polymorphous low‐grade adenocarcinoma: an appraisal of its origin and morphology

Background Polymorphous low‐grade adenocarcinoma (PLGA) remains a diagnostic challenge for most pathologists due to its large spectrum of histological patterns. In this study, the expression of two new markers recently described for salivary gland tumors was studied in PLGA. Methods The morphology o...

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Veröffentlicht in:Journal of oral pathology & medicine 2017-03, Vol.46 (3), p.182-187
Hauptverfasser: Montalli, Victor Angelo Martins, Passador‐Santos, Fabricio, Martinez, Elizabeth Ferreira, Furuse, Cristiane, Aguiar, Maria Cássia, Soares, Fernando Augusto, Soares, Andresa Borges, Brown, Amy Louise, Araújo, Ney Soares, Araújo, Vera Cavalcanti
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container_issue 3
container_start_page 182
container_title Journal of oral pathology & medicine
container_volume 46
creator Montalli, Victor Angelo Martins
Passador‐Santos, Fabricio
Martinez, Elizabeth Ferreira
Furuse, Cristiane
Aguiar, Maria Cássia
Soares, Fernando Augusto
Soares, Andresa Borges
Brown, Amy Louise
Araújo, Ney Soares
Araújo, Vera Cavalcanti
description Background Polymorphous low‐grade adenocarcinoma (PLGA) remains a diagnostic challenge for most pathologists due to its large spectrum of histological patterns. In this study, the expression of two new markers recently described for salivary gland tumors was studied in PLGA. Methods The morphology of 33 cases of PLGA was carefully evaluated using hematoxylin‐and‐eosin‐stained sections and confirmed by immunohistochemistry for cytokeratin 7, vimentin, and S‐100. Periodic acid–Schiff with diastase digestion was also used. The expression of mammaglobin and DOG‐1 was carried out using the EnVision System. Mammaglobin was assessed according to the percentage of positively stained tumor cells, while DOG‐1 was evaluated according to its presence and site. For MCM‐2 and Ki‐67, markers of proliferation, the labeling index of cell nuclei positivity was evaluated using total cell number. The ETV6‐NTRK3 fusion was examined by fluorescence in situ hybridization analysis. Results The histological patterns of the tumor were classified as lobular or non‐lobular. For the non‐lobular pattern, tubular, cribriform, glomeruliform, trabecular, and papillary patterns were observed. Mammaglobin was present in all PLGA cases, and its expression was stronger (P = 0.01) in the lobular than in the non‐lobular pattern. The expression of DOG‐1 was present in the apical portion and cytoplasm of the cells. Proliferation markers were low for all cases independent of histological pattern. Conclusions Polymorphous low‐grade adenocarcinoma has been confirmed to originate from the intercalated duct and to feature high expression of mammaglobin in its lobular pattern resembling that of mammary secretory analogue carcinoma, except for the ETV6 gene rearrangement.
doi_str_mv 10.1111/jop.12491
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In this study, the expression of two new markers recently described for salivary gland tumors was studied in PLGA. Methods The morphology of 33 cases of PLGA was carefully evaluated using hematoxylin‐and‐eosin‐stained sections and confirmed by immunohistochemistry for cytokeratin 7, vimentin, and S‐100. Periodic acid–Schiff with diastase digestion was also used. The expression of mammaglobin and DOG‐1 was carried out using the EnVision System. Mammaglobin was assessed according to the percentage of positively stained tumor cells, while DOG‐1 was evaluated according to its presence and site. For MCM‐2 and Ki‐67, markers of proliferation, the labeling index of cell nuclei positivity was evaluated using total cell number. The ETV6‐NTRK3 fusion was examined by fluorescence in situ hybridization analysis. Results The histological patterns of the tumor were classified as lobular or non‐lobular. For the non‐lobular pattern, tubular, cribriform, glomeruliform, trabecular, and papillary patterns were observed. Mammaglobin was present in all PLGA cases, and its expression was stronger (P = 0.01) in the lobular than in the non‐lobular pattern. The expression of DOG‐1 was present in the apical portion and cytoplasm of the cells. Proliferation markers were low for all cases independent of histological pattern. Conclusions Polymorphous low‐grade adenocarcinoma has been confirmed to originate from the intercalated duct and to feature high expression of mammaglobin in its lobular pattern resembling that of mammary secretory analogue carcinoma, except for the ETV6 gene rearrangement.</description><identifier>ISSN: 0904-2512</identifier><identifier>EISSN: 1600-0714</identifier><identifier>DOI: 10.1111/jop.12491</identifier><identifier>PMID: 27591391</identifier><language>eng</language><publisher>Denmark: Wiley Subscription Services, Inc</publisher><subject>Adenocarcinoma ; Adenocarcinoma - metabolism ; Adenocarcinoma - pathology ; Adult ; Aged ; Aged, 80 and over ; Anoctamin-1 - metabolism ; Biomarkers, Tumor - metabolism ; Cell fusion ; Cell number ; Cell proliferation ; Cytokeratin ; Cytoplasm ; Dentistry ; Digestion ; DOG‐1 ; Female ; Fluorescence in situ hybridization ; Gene rearrangement ; Humans ; Hybridization analysis ; Immunohistochemistry ; Male ; mammaglobin ; Mammaglobin A - metabolism ; Middle Aged ; Morphology ; Neoplasm Proteins - metabolism ; Nuclei ; Oral cancer ; origin ; Polylactide-co-glycolide ; polymorphous low‐grade adenocarcinoma ; Salivary gland ; Salivary Gland Neoplasms - metabolism ; Salivary Gland Neoplasms - pathology ; Tumor cells ; Tumors ; Vimentin</subject><ispartof>Journal of oral pathology &amp; medicine, 2017-03, Vol.46 (3), p.182-187</ispartof><rights>2016 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd</rights><rights>2016 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2017 John Wiley &amp; Sons A/S. 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In this study, the expression of two new markers recently described for salivary gland tumors was studied in PLGA. Methods The morphology of 33 cases of PLGA was carefully evaluated using hematoxylin‐and‐eosin‐stained sections and confirmed by immunohistochemistry for cytokeratin 7, vimentin, and S‐100. Periodic acid–Schiff with diastase digestion was also used. The expression of mammaglobin and DOG‐1 was carried out using the EnVision System. Mammaglobin was assessed according to the percentage of positively stained tumor cells, while DOG‐1 was evaluated according to its presence and site. For MCM‐2 and Ki‐67, markers of proliferation, the labeling index of cell nuclei positivity was evaluated using total cell number. The ETV6‐NTRK3 fusion was examined by fluorescence in situ hybridization analysis. Results The histological patterns of the tumor were classified as lobular or non‐lobular. For the non‐lobular pattern, tubular, cribriform, glomeruliform, trabecular, and papillary patterns were observed. Mammaglobin was present in all PLGA cases, and its expression was stronger (P = 0.01) in the lobular than in the non‐lobular pattern. The expression of DOG‐1 was present in the apical portion and cytoplasm of the cells. Proliferation markers were low for all cases independent of histological pattern. 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In this study, the expression of two new markers recently described for salivary gland tumors was studied in PLGA. Methods The morphology of 33 cases of PLGA was carefully evaluated using hematoxylin‐and‐eosin‐stained sections and confirmed by immunohistochemistry for cytokeratin 7, vimentin, and S‐100. Periodic acid–Schiff with diastase digestion was also used. The expression of mammaglobin and DOG‐1 was carried out using the EnVision System. Mammaglobin was assessed according to the percentage of positively stained tumor cells, while DOG‐1 was evaluated according to its presence and site. For MCM‐2 and Ki‐67, markers of proliferation, the labeling index of cell nuclei positivity was evaluated using total cell number. The ETV6‐NTRK3 fusion was examined by fluorescence in situ hybridization analysis. Results The histological patterns of the tumor were classified as lobular or non‐lobular. For the non‐lobular pattern, tubular, cribriform, glomeruliform, trabecular, and papillary patterns were observed. Mammaglobin was present in all PLGA cases, and its expression was stronger (P = 0.01) in the lobular than in the non‐lobular pattern. The expression of DOG‐1 was present in the apical portion and cytoplasm of the cells. Proliferation markers were low for all cases independent of histological pattern. Conclusions Polymorphous low‐grade adenocarcinoma has been confirmed to originate from the intercalated duct and to feature high expression of mammaglobin in its lobular pattern resembling that of mammary secretory analogue carcinoma, except for the ETV6 gene rearrangement.</abstract><cop>Denmark</cop><pub>Wiley Subscription Services, Inc</pub><pmid>27591391</pmid><doi>10.1111/jop.12491</doi><tpages>6</tpages></addata></record>
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subjects Adenocarcinoma
Adenocarcinoma - metabolism
Adenocarcinoma - pathology
Adult
Aged
Aged, 80 and over
Anoctamin-1 - metabolism
Biomarkers, Tumor - metabolism
Cell fusion
Cell number
Cell proliferation
Cytokeratin
Cytoplasm
Dentistry
Digestion
DOG‐1
Female
Fluorescence in situ hybridization
Gene rearrangement
Humans
Hybridization analysis
Immunohistochemistry
Male
mammaglobin
Mammaglobin A - metabolism
Middle Aged
Morphology
Neoplasm Proteins - metabolism
Nuclei
Oral cancer
origin
Polylactide-co-glycolide
polymorphous low‐grade adenocarcinoma
Salivary gland
Salivary Gland Neoplasms - metabolism
Salivary Gland Neoplasms - pathology
Tumor cells
Tumors
Vimentin
title Mammaglobin and DOG‐1 expression in polymorphous low‐grade adenocarcinoma: an appraisal of its origin and morphology
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