Malignancy Risk, Molecular Mutations, and Surgical Outcomes of Thyroid Nodules Classified as Atypia of Undetermined Significance in the Bethesda System: A Comprehensive Analysis.

IF 1.1 4区 医学 Q4 CELL BIOLOGY
Cytopathology Pub Date : 2025-04-24 DOI:10.1111/cyt.13503
Caroline Bourque, Gianluca Savoia, Maxine Noik, Livia Florianova, Saruchi Bandargal, Sabrina Daniela da Silva, Richard Payne, Marc Philippe Pusztaszeri
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引用次数: 0

Abstract

Objectives: Thyroid nodules classified as atypia of undetermined significance (AUS) within the Bethesda System for Reporting Thyroid Cytopathology (TBSRTC) present a diagnostic challenge, with a risk of malignancy (ROM) of 5% to 50%. In 2017, TBSRTC introduced AUS subcategories to enhance ROM assessment. This study explores the correlation between AUS subclassification, molecular mutations, and surgical outcomes.

Methods: Retrospective analysis was performed of 114 AUS cases with molecular profiling by ThyroSeqV3 and surgical follow-up. AUS subcategories as defined by TBSRTC included: AUS-Architectural, AUS-Nuclear, AUS-Nuclear and Architectural, and AUS-Hürthle cell. Pathology diagnoses were categorised as benign, malignant, or borderline, including noninvasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP).

Results: Of the 114 nodules, 32.5% were AUS-Architectural, 28.9% AUS-Nuclear and Architectural, 18.4% AUS-Nuclear, 19.3% AUS-Hürthle cell, and 0.9% AUS-Not Otherwise Specified. Papillary carcinoma, predominantly follicular variant, was the most common diagnosis (47.4%), followed by benign lesions (34.2%) and NIFTP (9.6%). RAS family mutations were the most prevalent molecular alteration (34.2%) followed by DICER1, EIF1AX, EXH1 mutations, CNA and GEP (29.8%). THADA fusions, PTEN, TSHR and BRAFK601E mutations were identified in 10.5% of cases, while high-risk mutations such as BRAF V600E, TERT, and TP53 were found in 8.8% of cases. AUS subcategories demonstrated distinct molecular profiles and were linked to varying surgical outcomes.

Conclusions: AUS subcategorization is associated with specific molecular profiles and surgical outcomes, supporting the subclassification of AUS cases per TBSRTC guidelines for improved risk stratification and clinical management. Further prospective studies with larger cohorts are necessary for validation.

在Bethesda系统中,恶性肿瘤风险、分子突变和分类为不确定异型甲状腺结节的手术结果:综合分析。
目的:在Bethesda甲状腺细胞病理学报告系统(TBSRTC)中,甲状腺结节被分类为不确定意义的非典型性(AUS),其诊断具有挑战性,恶性肿瘤(ROM)的风险为5%至50%。2017年,TBSRTC引入了AUS子类别,以加强ROM评估。本研究探讨了AUS亚型、分子突变和手术结果之间的关系。方法:对114例AUS患者进行回顾性分析,采用ThyroSeqV3进行分子谱分析,并进行手术随访。由TBSRTC定义的AUS子类别包括:AUS-Architectural, AUS- nuclear, AUS- nuclear and Architectural,以及AUS- hrthle cell。病理诊断分为良性、恶性或交界性,包括具有乳头状样核特征的非侵袭性滤泡性甲状腺肿瘤(NIFTP)。结果:114例结节中,32.5%为auss -Architectural, 28.9%为auss - nuclear and Architectural, 18.4%为auss - nuclear, 19.3%为auss - h rthle细胞,0.9%为auss - other Specified。乳头状癌,主要是滤泡变异,是最常见的诊断(47.4%),其次是良性病变(34.2%)和NIFTP(9.6%)。RAS家族突变是最常见的分子改变(34.2%),其次是DICER1、EIF1AX、EXH1突变、CNA和GEP(29.8%)。在10.5%的病例中发现了ada融合、PTEN、TSHR和BRAFK601E突变,而在8.8%的病例中发现了BRAF V600E、TERT和TP53等高风险突变。AUS亚型表现出不同的分子特征,并与不同的手术结果有关。结论:AUS亚分类与特定的分子特征和手术结果相关,支持根据TBSRTC指南对AUS病例进行亚分类,以改善风险分层和临床管理。进一步的前瞻性研究需要更大的队列来验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cytopathology
Cytopathology 生物-病理学
CiteScore
2.30
自引率
15.40%
发文量
107
审稿时长
6-12 weeks
期刊介绍: The aim of Cytopathology is to publish articles relating to those aspects of cytology which will increase our knowledge and understanding of the aetiology, diagnosis and management of human disease. It contains original articles and critical reviews on all aspects of clinical cytology in its broadest sense, including: gynaecological and non-gynaecological cytology; fine needle aspiration and screening strategy. Cytopathology welcomes papers and articles on: ultrastructural, histochemical and immunocytochemical studies of the cell; quantitative cytology and DNA hybridization as applied to cytological material.
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