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      Indeterminate thyroid cytology: detecting malignancy using analysis of nuclear images

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          Abstract

          Background

          Thyroid nodules diagnosed as 'atypia of undetermined significance/follicular lesion of undetermined significance' (AUS/FLUS) or 'follicular neoplasm/suspected follicular neoplasm' (FN/SFN), according to Bethesda’s classification, represent a challenge in clinical practice. Computerized analysis of nuclear images (CANI) could be a useful tool for these cases. Our aim was to evaluate the ability of CANI to correctly classify AUS/FLUS and FN/SFN thyroid nodules for malignancy.

          Methods

          We studied 101 nodules cytologically classified as AUS/FLUS ( n = 68) or FN/SFN ( n = 33) from 97 thyroidectomy patients. Slides with cytological material were submitted for manual selection and analysis of the follicular cell nuclei for morphometric and texture parameters using ImageJ software. The histologically benign and malignant lesions were compared for such parameters which were then evaluated for the capacity to predict malignancy using the classification and regression trees gini model. The intraclass coefficient of correlation was used to evaluate method reproducibility.

          Results

          In AUS/FLUS nodule analysis, the benign and malignant nodules differed for entropy ( P < 0.05), while the FN/SFN nodules differed for fractal analysis, coefficient of variation (CV) of roughness, and CV-entropy ( P < 0.05). Considering the AUS/FLUS and FN/SFN nodules separately, it correctly classified 90.0 and 100.0% malignant nodules, with a correct global classification of 94.1 and 97%, respectively. We observed that reproducibility was substantially or nearly complete (0.61–0.93) in 10 of the 12 nuclear parameters evaluated.

          Conclusion

          CANI demonstrated a high capacity for correctly classifying AUS/FLUS and FN/SFN thyroid nodules for malignancy. This could be a useful method to help increase diagnostic accuracy in the indeterminate thyroid cytology.

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          Most cited references23

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          The 2017 Bethesda System for Reporting Thyroid Cytopathology.

          The Bethesda System for Reporting Thyroid Cytopathology (TBSRTC) established a standardized, category-based reporting system for thyroid fine-needle aspiration (FNA) specimens. The 2017 revision reaffirms that every thyroid FNA report should begin with one of six diagnostic categories, the names of which remain unchanged since they were first introduced: (i) nondiagnostic or unsatisfactory; (ii) benign; (iii) atypia of undetermined significance (AUS) or follicular lesion of undetermined significance (FLUS); (iv) follicular neoplasm or suspicious for a follicular neoplasm; (v) suspicious for malignancy; and (vi) malignant. There is a choice of two different names for some of the categories. A laboratory should choose the one it prefers and use it exclusively for that category. Synonymous terms (e.g., AUS and FLUS) should not be used to denote two distinct interpretations. Each category has an implied cancer risk that ranges from 0% to 3% for the "benign" category to virtually 100% for the "malignant" category, and, in the 2017 revision, the malignancy risks have been updated based on new (post 2010) data. As a function of their risk associations, each category is linked to updated, evidence-based clinical management recommendations. The recent reclassification of some thyroid neoplasms as noninvasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP) has implications for the risk of malignancy, and this is accounted for with regard to diagnostic criteria and optional notes. Such notes can be useful in helping guide surgical management.
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            Classification and regression trees

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              The Bethesda System for Reporting Thyroid Cytopathology: a meta-analysis.

              We aimed to investigate the validity of the Bethesda System for Reporting Thyroid Cytopathology (TBSRTC) through meta-analysis. All publications between January 1, 2008 and September 1, 2011 that studied TBSRTC and had available histological follow-up data were retrieved. To calculate the sensitivity, specificity and diagnostic accuracy, the cases diagnosed as follicular neoplasm, suspicious for malignancy and malignant which were histopathologically confirmed as malignant were defined as true-positive. True-negative included benign cases confirmed as benign on histopathology. The nondiagnostic category was excluded from the statistical calculation. The correlations between the 6 diagnostic categories were investigated. The publications review resulted in a case cohort of 25,445 thyroid fine-needle aspirations, 6,362 (25%) of which underwent surgical excision; this group constituted the basis of the study. The sensitivity, specificity and diagnostic accuracy were 97, 50.7 and 68.8%, respectively. The positive predictive value and negative predictive value were 55.9 and 96.3%, respectively. The rates of false negatives and false positives were low: 3 and 0.5%, respectively. The results of meta-analysis showed high overall accuracy, indicating that TBSRTC represents a reliable and valid reporting system for thyroid cytology. Copyright © 2012 S. Karger AG, Basel.

                Author and article information

                Journal
                Endocr Connect
                Endocr Connect
                EC
                Endocrine Connections
                Bioscientifica Ltd (Bristol )
                2049-3614
                02 June 2021
                01 July 2021
                : 10
                : 7
                : 707-714
                Affiliations
                [1 ]Department of Internal Medicine , Botucatu Medical School, Sao Paulo State University (Unesp), Botucatu, São Paulo, Brazil
                [2 ]Department of Pathology , Botucatu Medical School, Sao Paulo State University (Unesp), Botucatu, São Paulo, Brazil
                [3 ]Department of Surgery and Orthopedics , Botucatu Medical School, Sao Paulo State University (Unesp), Botucatu, São Paulo, Brazil
                [4 ]Department of Dermatology , Botucatu Medical School, Sao Paulo State University (Unesp), Botucatu, São Paulo, Brazil
                [5 ]Department of Otolaryngology and Head and Neck Surgery , Botucatu Medical School, Sao Paulo State University (Unesp), Botucatu, São Paulo, Brazil
                [6 ]Instituto de Investigação e Inovação em Saúde (i3S) , Universidade do Porto, Porto, Portugal
                [7 ]Cancer Signaling and Metabolism Group , Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal
                [8 ]Department of Pathology , Medical Faculty of the University of Porto, Porto, Portugal
                Author notes
                Correspondence should be addressed to G M F S Mazeto: g.mazeto@ 123456unesp.br

                *(C Y Hayashi and D T A Jaune contributed equally to this work)

                Author information
                http://orcid.org/0000-0003-2129-7256
                Article
                EC-20-0648
                10.1530/EC-20-0648
                8284953
                34077391
                1cbd5630-955c-43b4-bba9-962898ed50fc
                © The authors

                This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

                History
                : 26 April 2021
                : 02 June 2021
                Categories
                Research

                cell nucleus,cytology,diagnosis,photography,thyroid neoplasms

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