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GATA3 expression in clear cell adenocarcinoma of the lower urinary tract: a potential diagnostic pitfall

BACKGROUND: Clear cell adenocarcinoma of the lower urinary tract (CCACLUT) is a rare primary malignant neoplasm with heterogenous morphology. There is a paucity of data in the literature regarding its immunohistochemical profile. METHODS: The immunohistochemical features (extent and intensity) of a...

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Autores principales: Akgul, Mahmut, Humble, Robert, Osme, Abdullah, Yuce, Servet, Kocak, Elif N., Najafzadeh, Parisa, Sangoi, Ankur, Pattnaik, Niharika, Mishra, Sourav, Sharma, Shivani, Shaker, Nada, Kaushal, Seema, Baisakh, Manas, Lightle, Andrea R., Balzer, Bonnie L., Xiao, Guang-Qian, MacLennan, Gregory T., Osunkoya, Adeboye O., Parwani, Anil, Cheng, Liang, Bellizzi, Andrew, Mohanty, Sambit K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9623977/
https://www.ncbi.nlm.nih.gov/pubmed/36320040
http://dx.doi.org/10.1186/s13000-022-01269-6
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author Akgul, Mahmut
Humble, Robert
Osme, Abdullah
Yuce, Servet
Kocak, Elif N.
Najafzadeh, Parisa
Sangoi, Ankur
Pattnaik, Niharika
Mishra, Sourav
Sharma, Shivani
Shaker, Nada
Kaushal, Seema
Baisakh, Manas
Lightle, Andrea R.
Balzer, Bonnie L.
Xiao, Guang-Qian
MacLennan, Gregory T.
Osunkoya, Adeboye O.
Parwani, Anil
Cheng, Liang
Bellizzi, Andrew
Mohanty, Sambit K.
author_facet Akgul, Mahmut
Humble, Robert
Osme, Abdullah
Yuce, Servet
Kocak, Elif N.
Najafzadeh, Parisa
Sangoi, Ankur
Pattnaik, Niharika
Mishra, Sourav
Sharma, Shivani
Shaker, Nada
Kaushal, Seema
Baisakh, Manas
Lightle, Andrea R.
Balzer, Bonnie L.
Xiao, Guang-Qian
MacLennan, Gregory T.
Osunkoya, Adeboye O.
Parwani, Anil
Cheng, Liang
Bellizzi, Andrew
Mohanty, Sambit K.
author_sort Akgul, Mahmut
collection PubMed
description BACKGROUND: Clear cell adenocarcinoma of the lower urinary tract (CCACLUT) is a rare primary malignant neoplasm with heterogenous morphology. There is a paucity of data in the literature regarding its immunohistochemical profile. METHODS: The immunohistochemical features (extent and intensity) of a multinational cohort of CCACLUT were evaluated with comparison between clear cell adenocarcinoma of the female genital tract (CCACFGT, tissue microarray) and nephrogenic adenoma (NA). RESULTS: 33 CCACLUT (24 female, 9 male; mean age 59 years) were collected. CCACLUT most commonly arose from the urinary bladder (26/33, 78%), particularly from the trigone (10/33, 30.3%) followed by the urethra (8/33, 22%). All 12 NA cases were located at the urinary bladder, whereas the most common CCACFGT location was the ovary (29/56, 52%). None of the CCACLUT patients had, intestinal metaplasia, NA, or urothelial carcinoma. One patient had concurrent endometriosis of the sigmoid colon. Most frequently observed morphology in CCACLUT was papillary/tubulocystic (9/3; 27.3%), followed by papillary/tubular (6/33; 18.2%) and papillary/solid (5/33; 15.2%). GATA3 expression was significantly higher in CCACLUT (18/33, 54.5%) and NA (6/12, 50%), when compared to CCACFGT cases 6/56, 11.7%)(p = 0.001 and p = 0.022, respectively). The extent of GATA3 was significantly higher in CCACLUT group (19.2 ± 16.6%) than the other groups (9.6 ± 22.5% in NA and 2.6 ± 9% in CCACFGT group) (p = 0.001). 4/33 patients (12.1) had weak, 10/33 patients (30.3%) had moderate, and 4/33 patients (12.1%) had strong GATA3 intensity in CCACLUT group. In NA group, one patient (8.3%, 1/12) had weak, one patient (8.3%, 1/12) had moderate and 4 patients (33.3%, 4/12) had strong GATA3 intensity. Most cases (CCACLUT 29/33, 88%; NA 11/12, 92%; CCACFGT 46/56, 82.1%) had positive Napsin A expression, by which CCACLUT had significantly more cases with Napsin A expression (p = 0.034). p63 was consistently negative in all cases (30/33 (91.9%) CCACLUT; 12/12 (100%) NA; 42/56 (75%) CCACFGT. Ki67 (MIB) proliferation index was significantly higher in CCACLUT group (54.6 ± 21%) when compared to NA group (4.5 ± 2.7%) and CCACFGT group (35.5 ± 25.8%) (p = 0.001). CONCLUSION: CCACLUT has consistent GATA3 expression, which may cause challenge in the diagnosis of urothelial carcinoma but can be used to distinguish CCACLUT from CCACFGT.
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spelling pubmed-96239772022-11-02 GATA3 expression in clear cell adenocarcinoma of the lower urinary tract: a potential diagnostic pitfall Akgul, Mahmut Humble, Robert Osme, Abdullah Yuce, Servet Kocak, Elif N. Najafzadeh, Parisa Sangoi, Ankur Pattnaik, Niharika Mishra, Sourav Sharma, Shivani Shaker, Nada Kaushal, Seema Baisakh, Manas Lightle, Andrea R. Balzer, Bonnie L. Xiao, Guang-Qian MacLennan, Gregory T. Osunkoya, Adeboye O. Parwani, Anil Cheng, Liang Bellizzi, Andrew Mohanty, Sambit K. Diagn Pathol Research BACKGROUND: Clear cell adenocarcinoma of the lower urinary tract (CCACLUT) is a rare primary malignant neoplasm with heterogenous morphology. There is a paucity of data in the literature regarding its immunohistochemical profile. METHODS: The immunohistochemical features (extent and intensity) of a multinational cohort of CCACLUT were evaluated with comparison between clear cell adenocarcinoma of the female genital tract (CCACFGT, tissue microarray) and nephrogenic adenoma (NA). RESULTS: 33 CCACLUT (24 female, 9 male; mean age 59 years) were collected. CCACLUT most commonly arose from the urinary bladder (26/33, 78%), particularly from the trigone (10/33, 30.3%) followed by the urethra (8/33, 22%). All 12 NA cases were located at the urinary bladder, whereas the most common CCACFGT location was the ovary (29/56, 52%). None of the CCACLUT patients had, intestinal metaplasia, NA, or urothelial carcinoma. One patient had concurrent endometriosis of the sigmoid colon. Most frequently observed morphology in CCACLUT was papillary/tubulocystic (9/3; 27.3%), followed by papillary/tubular (6/33; 18.2%) and papillary/solid (5/33; 15.2%). GATA3 expression was significantly higher in CCACLUT (18/33, 54.5%) and NA (6/12, 50%), when compared to CCACFGT cases 6/56, 11.7%)(p = 0.001 and p = 0.022, respectively). The extent of GATA3 was significantly higher in CCACLUT group (19.2 ± 16.6%) than the other groups (9.6 ± 22.5% in NA and 2.6 ± 9% in CCACFGT group) (p = 0.001). 4/33 patients (12.1) had weak, 10/33 patients (30.3%) had moderate, and 4/33 patients (12.1%) had strong GATA3 intensity in CCACLUT group. In NA group, one patient (8.3%, 1/12) had weak, one patient (8.3%, 1/12) had moderate and 4 patients (33.3%, 4/12) had strong GATA3 intensity. Most cases (CCACLUT 29/33, 88%; NA 11/12, 92%; CCACFGT 46/56, 82.1%) had positive Napsin A expression, by which CCACLUT had significantly more cases with Napsin A expression (p = 0.034). p63 was consistently negative in all cases (30/33 (91.9%) CCACLUT; 12/12 (100%) NA; 42/56 (75%) CCACFGT. Ki67 (MIB) proliferation index was significantly higher in CCACLUT group (54.6 ± 21%) when compared to NA group (4.5 ± 2.7%) and CCACFGT group (35.5 ± 25.8%) (p = 0.001). CONCLUSION: CCACLUT has consistent GATA3 expression, which may cause challenge in the diagnosis of urothelial carcinoma but can be used to distinguish CCACLUT from CCACFGT. BioMed Central 2022-11-01 /pmc/articles/PMC9623977/ /pubmed/36320040 http://dx.doi.org/10.1186/s13000-022-01269-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Akgul, Mahmut
Humble, Robert
Osme, Abdullah
Yuce, Servet
Kocak, Elif N.
Najafzadeh, Parisa
Sangoi, Ankur
Pattnaik, Niharika
Mishra, Sourav
Sharma, Shivani
Shaker, Nada
Kaushal, Seema
Baisakh, Manas
Lightle, Andrea R.
Balzer, Bonnie L.
Xiao, Guang-Qian
MacLennan, Gregory T.
Osunkoya, Adeboye O.
Parwani, Anil
Cheng, Liang
Bellizzi, Andrew
Mohanty, Sambit K.
GATA3 expression in clear cell adenocarcinoma of the lower urinary tract: a potential diagnostic pitfall
title GATA3 expression in clear cell adenocarcinoma of the lower urinary tract: a potential diagnostic pitfall
title_full GATA3 expression in clear cell adenocarcinoma of the lower urinary tract: a potential diagnostic pitfall
title_fullStr GATA3 expression in clear cell adenocarcinoma of the lower urinary tract: a potential diagnostic pitfall
title_full_unstemmed GATA3 expression in clear cell adenocarcinoma of the lower urinary tract: a potential diagnostic pitfall
title_short GATA3 expression in clear cell adenocarcinoma of the lower urinary tract: a potential diagnostic pitfall
title_sort gata3 expression in clear cell adenocarcinoma of the lower urinary tract: a potential diagnostic pitfall
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9623977/
https://www.ncbi.nlm.nih.gov/pubmed/36320040
http://dx.doi.org/10.1186/s13000-022-01269-6
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