Literature DB >> 29596039

Subclassification of Bethesda Atypical and Follicular Neoplasm Categories According to Nuclear and Architectural Atypia Improves Discrimination of Thyroid Malignancy Risk.

Joel Xue Yi Lim1, Min En Nga2, Dedrick Kok Hong Chan3, Wee Boon Tan4, Rajeev Parameswaran4, Kee Yuan Ngiam4.   

Abstract

BACKGROUND: Although The Bethesda System for Reporting Thyroid Cytopathology has provided clinicians with a standardized classification scheme for the diagnosis of thyroid fine-needle aspiration cytology (FNAC) specimens, the indeterminate categories of Bethesda III (B3)-atypia of undetermined significance/follicular lesion of undetermined significance (AUS/FLUS)-and Bethesda IV (B4)-follicular neoplasm/suspicious for follicular neoplasm (FN/SFN)-continue to pose challenges with regards to ideal diagnostic and therapeutic management. Having previously demonstrated the presence of nuclear atypia as a high-risk subgroup in B3, the objective of this study was to evaluate the malignancy rates in the B4 subgroup with nuclear atypia.
METHODS: A retrospective review of all thyroid FNACs diagnosed as B4 (FN/SFN) between 2008 and 2015 was conducted at a tertiary referral center in Singapore. Data on patient demographics, sonographic features, and final histological diagnosis were collected. This was compared to data from a previous analysis on all nodules diagnosed as B3 (AUS/FLUS) over a similar period.
RESULTS: A total of 137/309 (44.3%) and 88/111 (79.3%) FNACs diagnosed as B3 and B4, respectively, underwent surgical excision yielding final histopathological diagnoses. The malignancy rate of B4 was 31/88 (35.2%) compared to B3, which was 37/137 (27.0%). Subclassification based on the presence of architectural versus nuclear atypia showed significantly higher malignancy rates in B4 nodules with nuclear atypia (21.8% vs. 57.6%; p < 0.01). These findings corroborate previous results within the B3 category (malignancy rate of 14.7% vs. 36.8%; p < 0.01). The only sonographic features predictive of malignancy were the presence of macrocalcifications in B4 compared to irregularity of margins in B3.
CONCLUSION: The presence of nuclear atypia identifies subgroups with significant differential malignancy risks within both the B3 and B4 categories. This supports the notion that subclassification is a useful risk stratification tool that can guide diagnostic and therapeutic management of indeterminate thyroid nodules with heterogenous risk profiles.

Entities:  

Keywords:  Bethesda classification; atypia of undetermined significance (AUS)/follicular lesion of undetermined significance (FLUS); fine-needle aspiration cytology; follicular neoplasm (FN)/suspicious for follicular neoplasm (SFN); malignancy risk; thyroid

Mesh:

Year:  2018        PMID: 29596039     DOI: 10.1089/thy.2017.0274

Source DB:  PubMed          Journal:  Thyroid        ISSN: 1050-7256            Impact factor:   6.568


  9 in total

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2.  The diversities in thyroid cytopathology practices among Asian countries using the Bethesda system for reporting thyroid cytopathology.

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4.  Ultrasound characteristics of thyroid nodules facilitate interpretation of the malignant risk of Bethesda system III/IV thyroid nodules and inform therapeutic schedule.

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5.  Comparison of Korean vs. American Thyroid Imaging Reporting and Data System in Malignancy Risk Assessment of Indeterminate Thyroid Nodules.

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6.  Predictors of Malignancy in Thyroid Nodules Classified as Bethesda Category III.

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Authors:  Won Sang Yoo; Hwa Young Ahn; Hye Shin Ahn; Yun Jae Chung; Hee Sung Kim; Bo Youn Cho; Mirinae Seo; Jae Hoon Moon; Young Joo Park
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8.  Risk Stratification Study of Indeterminate Thyroid Nodules with a next-generation Sequencing Assay with Residual ThinPrep® Material.

Authors:  Huan Zhao; Weiwei Jing; Weihua Li; Zhihui Zhang; Jian Cao; Linlin Zhao; Yue Sun; Cong Wang; Yong Wang; Huiqin Guo
Journal:  J Cancer       Date:  2020-10-21       Impact factor: 4.207

9.  Indeterminate thyroid cytology: detecting malignancy using analysis of nuclear images.

Authors:  Caroline Y Hayashi; Danilo T A Jaune; Cristiano C Oliveira; Bárbara P Coelho; Hélio A Miot; Mariângela E A Marques; José Vicente Tagliarini; Emanuel C Castilho; Carlos S P Soares; Flávia R K Oliveira; Paula Soares; Gláucia M F S Mazeto
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  9 in total

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