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Milan System for Reporting Salivary Gland Cytopathology– An Experience from Western Indian Population

INTRODUCTION: Fine-needle aspiration cytology (FNAC) can be challenging to provide a precise diagnosis in salivary gland cytopathology due to diversity of lesions and cytomorphological convergence between the tumors and within the same tumor of salivary gland. The recently proposed Milan System for...

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Autores principales: Gaikwad, Vaishali P, Anupriya, Chanda, Naik, Leena P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315920/
https://www.ncbi.nlm.nih.gov/pubmed/32606497
http://dx.doi.org/10.4103/JOC.JOC_156_19
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author Gaikwad, Vaishali P
Anupriya, Chanda
Naik, Leena P
author_facet Gaikwad, Vaishali P
Anupriya, Chanda
Naik, Leena P
author_sort Gaikwad, Vaishali P
collection PubMed
description INTRODUCTION: Fine-needle aspiration cytology (FNAC) can be challenging to provide a precise diagnosis in salivary gland cytopathology due to diversity of lesions and cytomorphological convergence between the tumors and within the same tumor of salivary gland. The recently proposed Milan System for Reporting Salivary Gland Cytopathology (MSRSGC) provides a risk stratification-based classification system with an intrinsic risk of malignancy (ROM) for each diagnostic category, which aims to furnish useful information to the clinicians. This study was undertaken to evaluate the diagnostic utility and validity of MSRSGC. METHODS AND MATERIAL: In this retrospective study, FNAC done for all salivary gland lesions over a period of two years were retrieved. All cases were categorized according to MSRSGC and correlated with histopathological follow-up, wherever available. ROM was calculated for each category. RESULTS: The cases belong to following categories: non-diagnostic (1.27%), non-neoplastic (30.38%), atypia of undetermined significance (5.06%), benign neoplasm (46.84%), salivary gland neoplasm of uncertain malignant potential (1.27%), suspicious for malignancy (1.27%), and malignant (13.92%). Out of 79 cases, 50.63% had follow-up. The ROM were 0% for category II and IVa, 50% for category III, and 100% for category IVb, V, and VI. The sensitivity, specificity, positive predictive value, negative predictive value, and diagnostic accuracy were recorded as 77.78%, 100%, 100%, 91.3%, and 93.33%, respectively. CONCLUSIONS: Application of MSRSGC has immense value for standardization of reporting of salivary gland FNAC. Our data corresponds to the studies done worldwide and recommends the use of MSRSGC for future diagnostic purposes.
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spelling pubmed-73159202020-06-29 Milan System for Reporting Salivary Gland Cytopathology– An Experience from Western Indian Population Gaikwad, Vaishali P Anupriya, Chanda Naik, Leena P J Cytol Original Article INTRODUCTION: Fine-needle aspiration cytology (FNAC) can be challenging to provide a precise diagnosis in salivary gland cytopathology due to diversity of lesions and cytomorphological convergence between the tumors and within the same tumor of salivary gland. The recently proposed Milan System for Reporting Salivary Gland Cytopathology (MSRSGC) provides a risk stratification-based classification system with an intrinsic risk of malignancy (ROM) for each diagnostic category, which aims to furnish useful information to the clinicians. This study was undertaken to evaluate the diagnostic utility and validity of MSRSGC. METHODS AND MATERIAL: In this retrospective study, FNAC done for all salivary gland lesions over a period of two years were retrieved. All cases were categorized according to MSRSGC and correlated with histopathological follow-up, wherever available. ROM was calculated for each category. RESULTS: The cases belong to following categories: non-diagnostic (1.27%), non-neoplastic (30.38%), atypia of undetermined significance (5.06%), benign neoplasm (46.84%), salivary gland neoplasm of uncertain malignant potential (1.27%), suspicious for malignancy (1.27%), and malignant (13.92%). Out of 79 cases, 50.63% had follow-up. The ROM were 0% for category II and IVa, 50% for category III, and 100% for category IVb, V, and VI. The sensitivity, specificity, positive predictive value, negative predictive value, and diagnostic accuracy were recorded as 77.78%, 100%, 100%, 91.3%, and 93.33%, respectively. CONCLUSIONS: Application of MSRSGC has immense value for standardization of reporting of salivary gland FNAC. Our data corresponds to the studies done worldwide and recommends the use of MSRSGC for future diagnostic purposes. Wolters Kluwer - Medknow 2020 2020-04-02 /pmc/articles/PMC7315920/ /pubmed/32606497 http://dx.doi.org/10.4103/JOC.JOC_156_19 Text en Copyright: © 2020 Journal of Cytology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Gaikwad, Vaishali P
Anupriya, Chanda
Naik, Leena P
Milan System for Reporting Salivary Gland Cytopathology– An Experience from Western Indian Population
title Milan System for Reporting Salivary Gland Cytopathology– An Experience from Western Indian Population
title_full Milan System for Reporting Salivary Gland Cytopathology– An Experience from Western Indian Population
title_fullStr Milan System for Reporting Salivary Gland Cytopathology– An Experience from Western Indian Population
title_full_unstemmed Milan System for Reporting Salivary Gland Cytopathology– An Experience from Western Indian Population
title_short Milan System for Reporting Salivary Gland Cytopathology– An Experience from Western Indian Population
title_sort milan system for reporting salivary gland cytopathology– an experience from western indian population
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315920/
https://www.ncbi.nlm.nih.gov/pubmed/32606497
http://dx.doi.org/10.4103/JOC.JOC_156_19
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