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Tumour associated tissue eosinophilia as a predictor of locoregional recurrence in oral squamous cell carcinoma

Objectives: The increasing global burden of oral cancer has driven much of the focus of research to the determination of reliable prognostic markers which may have significant effects on survival and the control of post-treatment morbidity. This study was undertaken to evaluate tumour associated tis...

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Autores principales: Rakesh, Nagaraju, Devi, Yashoda, Majumdar, Kuhu, Reddy, Sujatha S., Agarwal, Kunal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medicina Oral S.L. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4367994/
https://www.ncbi.nlm.nih.gov/pubmed/25810818
http://dx.doi.org/10.4317/jced.51610
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author Rakesh, Nagaraju
Devi, Yashoda
Majumdar, Kuhu
Reddy, Sujatha S.
Agarwal, Kunal
author_facet Rakesh, Nagaraju
Devi, Yashoda
Majumdar, Kuhu
Reddy, Sujatha S.
Agarwal, Kunal
author_sort Rakesh, Nagaraju
collection PubMed
description Objectives: The increasing global burden of oral cancer has driven much of the focus of research to the determination of reliable prognostic markers which may have significant effects on survival and the control of post-treatment morbidity. This study was undertaken to evaluate tumour associated tissue eosinophilia (TATE) quantitatively in oral cancer specimens and observe for its possible association with tumour stage, patterns of locoregional recurrence and overall prognosis. Study Design: 14 patients undergoing surgical resection for primary oral squamous cell carcinoma (OSCC) were subjected to grey scale ultrasonography (USG) to assess tumour dimensions. The findings were compared with the cTNM stage initially documented. TATE was evaluated along the invasive tumour front (ITF) using H & E stained sections of histopathological specimens for 10 continuous high power fields (HPF) and graded as mild, moderate or intense. Patients were followed up over 5 years and observed for patterns of recurrence. Results: Loco regional recurrence was significantly associated with intense degree of TATE. (p<0.001) cTNM stage as well as USG stage did not correlate with the degree of TATE with p=0.419 and 0.772 respectively. None of the patients with mild/ moderate dysplasia developed locoregional recurrence within the period of follow up. Conclusions: Analysis of TATE in OSCC patients may provide an early indication of future locoregional recurrence. Identification of an appropriate biopsy site representing the ITF where TATE analysis can be performed may be a simple, inexpensive method of obtaining valuable prognostic information at the time of diagnosis. Key words:Tumour associated tissue eosinophilia, oral cancer, prognosis.
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spelling pubmed-43679942015-03-25 Tumour associated tissue eosinophilia as a predictor of locoregional recurrence in oral squamous cell carcinoma Rakesh, Nagaraju Devi, Yashoda Majumdar, Kuhu Reddy, Sujatha S. Agarwal, Kunal J Clin Exp Dent Research Objectives: The increasing global burden of oral cancer has driven much of the focus of research to the determination of reliable prognostic markers which may have significant effects on survival and the control of post-treatment morbidity. This study was undertaken to evaluate tumour associated tissue eosinophilia (TATE) quantitatively in oral cancer specimens and observe for its possible association with tumour stage, patterns of locoregional recurrence and overall prognosis. Study Design: 14 patients undergoing surgical resection for primary oral squamous cell carcinoma (OSCC) were subjected to grey scale ultrasonography (USG) to assess tumour dimensions. The findings were compared with the cTNM stage initially documented. TATE was evaluated along the invasive tumour front (ITF) using H & E stained sections of histopathological specimens for 10 continuous high power fields (HPF) and graded as mild, moderate or intense. Patients were followed up over 5 years and observed for patterns of recurrence. Results: Loco regional recurrence was significantly associated with intense degree of TATE. (p<0.001) cTNM stage as well as USG stage did not correlate with the degree of TATE with p=0.419 and 0.772 respectively. None of the patients with mild/ moderate dysplasia developed locoregional recurrence within the period of follow up. Conclusions: Analysis of TATE in OSCC patients may provide an early indication of future locoregional recurrence. Identification of an appropriate biopsy site representing the ITF where TATE analysis can be performed may be a simple, inexpensive method of obtaining valuable prognostic information at the time of diagnosis. Key words:Tumour associated tissue eosinophilia, oral cancer, prognosis. Medicina Oral S.L. 2015-02-01 /pmc/articles/PMC4367994/ /pubmed/25810818 http://dx.doi.org/10.4317/jced.51610 Text en Copyright: © 2015 Medicina Oral S.L. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Rakesh, Nagaraju
Devi, Yashoda
Majumdar, Kuhu
Reddy, Sujatha S.
Agarwal, Kunal
Tumour associated tissue eosinophilia as a predictor of locoregional recurrence in oral squamous cell carcinoma
title Tumour associated tissue eosinophilia as a predictor of locoregional recurrence in oral squamous cell carcinoma
title_full Tumour associated tissue eosinophilia as a predictor of locoregional recurrence in oral squamous cell carcinoma
title_fullStr Tumour associated tissue eosinophilia as a predictor of locoregional recurrence in oral squamous cell carcinoma
title_full_unstemmed Tumour associated tissue eosinophilia as a predictor of locoregional recurrence in oral squamous cell carcinoma
title_short Tumour associated tissue eosinophilia as a predictor of locoregional recurrence in oral squamous cell carcinoma
title_sort tumour associated tissue eosinophilia as a predictor of locoregional recurrence in oral squamous cell carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4367994/
https://www.ncbi.nlm.nih.gov/pubmed/25810818
http://dx.doi.org/10.4317/jced.51610
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