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Study of histopathological features and proliferation markers in cases of Wilms’ tumor

CONTEXT: The spectrum of pediatric renal tumors is different from adult renal tumors, and Wilms’ tumor (WT) forms the majority. The histological type and clinicopathological staging are the two important prognostic parameters. The role of newer prognostic factors is not clear. AIMS: This study was p...

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Autores principales: Das, Ram Narayan, Chatterjee, Uttara, Sinha, Swapan K., Ray, Ashoke K., Saha, Koushik, Banerjee, Sugato
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3439786/
https://www.ncbi.nlm.nih.gov/pubmed/22988352
http://dx.doi.org/10.4103/0971-5851.99744
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author Das, Ram Narayan
Chatterjee, Uttara
Sinha, Swapan K.
Ray, Ashoke K.
Saha, Koushik
Banerjee, Sugato
author_facet Das, Ram Narayan
Chatterjee, Uttara
Sinha, Swapan K.
Ray, Ashoke K.
Saha, Koushik
Banerjee, Sugato
author_sort Das, Ram Narayan
collection PubMed
description CONTEXT: The spectrum of pediatric renal tumors is different from adult renal tumors, and Wilms’ tumor (WT) forms the majority. The histological type and clinicopathological staging are the two important prognostic parameters. The role of newer prognostic factors is not clear. AIMS: This study was performed to analyze the histopathological spectrum of pediatric renal tumors and to study the expression of proliferation markers (Ki-67 and p53) in WT and correlate its expression in epithelial and blastema components in different stages. MATERIALS AND METHODS: Twenty-seven cases of pediatric renal tumors were collected over 2 years. Hematoxylin-eosin staining was used for diagnosis. Immunostaining was performed for Ki-67 and p53. Ki-67 proliferation index (PI) and p53 expression were determined in each case and for the epithelial and blastema components separately. STATISTICAL ANALYSIS AND RESULTS: We had 20 cases of WT (74.1%), three cases of mesoblastic nephroma (11.1%), three cases of clear cell sarcoma (11.1%) and one case of rhabdoid tumor (3.7%). It was observed that the PI of the epithelial component (57.2%) was significantly higher than that of blastema (39.53%) in all stages. The PI in Stage II is significantly higher than that in Stage I. Statistical analysis could not be performed in Stages III and IV due to the small number of cases. p53 expression did not show any significant difference in the epithelial and blastema components. There was also no significant difference between the stages. CONCLUSION: In this study, we found the differences between PI of different tissue components of WT, with the epithelial component having a higher PI, which correlated with the stage of advancement of the disease.
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spelling pubmed-34397862012-09-17 Study of histopathological features and proliferation markers in cases of Wilms’ tumor Das, Ram Narayan Chatterjee, Uttara Sinha, Swapan K. Ray, Ashoke K. Saha, Koushik Banerjee, Sugato Indian J Med Paediatr Oncol Original Article CONTEXT: The spectrum of pediatric renal tumors is different from adult renal tumors, and Wilms’ tumor (WT) forms the majority. The histological type and clinicopathological staging are the two important prognostic parameters. The role of newer prognostic factors is not clear. AIMS: This study was performed to analyze the histopathological spectrum of pediatric renal tumors and to study the expression of proliferation markers (Ki-67 and p53) in WT and correlate its expression in epithelial and blastema components in different stages. MATERIALS AND METHODS: Twenty-seven cases of pediatric renal tumors were collected over 2 years. Hematoxylin-eosin staining was used for diagnosis. Immunostaining was performed for Ki-67 and p53. Ki-67 proliferation index (PI) and p53 expression were determined in each case and for the epithelial and blastema components separately. STATISTICAL ANALYSIS AND RESULTS: We had 20 cases of WT (74.1%), three cases of mesoblastic nephroma (11.1%), three cases of clear cell sarcoma (11.1%) and one case of rhabdoid tumor (3.7%). It was observed that the PI of the epithelial component (57.2%) was significantly higher than that of blastema (39.53%) in all stages. The PI in Stage II is significantly higher than that in Stage I. Statistical analysis could not be performed in Stages III and IV due to the small number of cases. p53 expression did not show any significant difference in the epithelial and blastema components. There was also no significant difference between the stages. CONCLUSION: In this study, we found the differences between PI of different tissue components of WT, with the epithelial component having a higher PI, which correlated with the stage of advancement of the disease. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3439786/ /pubmed/22988352 http://dx.doi.org/10.4103/0971-5851.99744 Text en Copyright: © Indian Journal of Medical and Paediatric Oncology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Das, Ram Narayan
Chatterjee, Uttara
Sinha, Swapan K.
Ray, Ashoke K.
Saha, Koushik
Banerjee, Sugato
Study of histopathological features and proliferation markers in cases of Wilms’ tumor
title Study of histopathological features and proliferation markers in cases of Wilms’ tumor
title_full Study of histopathological features and proliferation markers in cases of Wilms’ tumor
title_fullStr Study of histopathological features and proliferation markers in cases of Wilms’ tumor
title_full_unstemmed Study of histopathological features and proliferation markers in cases of Wilms’ tumor
title_short Study of histopathological features and proliferation markers in cases of Wilms’ tumor
title_sort study of histopathological features and proliferation markers in cases of wilms’ tumor
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3439786/
https://www.ncbi.nlm.nih.gov/pubmed/22988352
http://dx.doi.org/10.4103/0971-5851.99744
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