Malignant risk of pediatric Bethesda category III thyroid nodules subcategorized by nuclear atypia and other: A single institution experience

IF 2.6 3区 医学 Q3 ONCOLOGY Cancer Cytopathology Pub Date : 2024-05-21 DOI:10.1002/cncy.22831
Xiaobing Jin MD, Xin Jing MD, Brian Smola BS, Amer Heider MD
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Abstract

Background

The 2023 Bethesda System for Reporting Thyroid Cytopathology (TBSRTC) divides AUS diagnoses into two major subcategories: atypia of undetermined significance (AUS) nuclear atypia (AUS-N) and other (AUS-O). This study aims to compare the histological outcome and malignant rate of pediatric AUS thyroid nodules classified into AUS-N and AUS-O subcategories.

Design

A search of our institutional electronic pathology database for the period from January 2012 to July 2023 was conducted to identify pediatric (<21 years old) thyroid nodules that were interpreted as AUS and subsequently had surgery. Cases were further divided into AUS-N and AUS-O subcategories. Results of follow-up surgical resections were collected. The malignant rate was calculated and compared between AUS-N and AUS-O groups.

Results

The study identified 62 thyroid nodules from 58 pediatric patients. Among these nodules, 29 and 33 were subcategorized as AUS-N and AUS-O, respectively. Both groups exhibited a female predominance and displayed a similar nodule size distribution. Histological analysis revealed 15 carcinomas in AUS-N nodules, including 11 cases of classic papillary thyroid carcinoma (PTC) and four cases of follicular type of PTC. In contrast, in the AUS-O group, a total of five carcinomas were documented, including two PTCs and three oncocytic thyroid carcinomas. Notably, the malignant rate of AUS-N nodules (52%) is significantly higher than that of AUS-O nodules (15%) (p = .002).

Conclusion

In pediatric AUS thyroid nodules, the malignant risk in AUS-N is significantly higher than that in AUS-O. These findings may guide more appropriate clinical triage and/or improve management of pediatric patients with AUS thyroid nodules.

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按核不典型性和其他分类的小儿贝塞斯达III类甲状腺结节的恶性风险:单一机构的经验。
背景:2023年贝塞斯达甲状腺细胞病理学报告系统(TBSRTC)将AUS诊断分为两大亚类:意义未定的不典型性(AUS)核不典型性(AUS-N)和其他(AUS-O)。本研究旨在比较分为AUS-N和AUS-O亚类的小儿AUS甲状腺结节的组织学结果和恶性率:设计:对本院2012年1月至2023年7月期间的电子病理数据库进行检索,以确定小儿AUS甲状腺结节的组织学结果和恶性率:研究发现了58名儿科患者的62个甲状腺结节。在这些结节中,29 个和 33 个分别被细分为 AUS-N 和 AUS-O。两组患者均以女性为主,结节大小分布相似。组织学分析显示,AUS-N结节中有15个癌瘤,包括11例典型甲状腺乳头状癌(PTC)和4例滤泡型PTC。而在AUS-O组中,共发现了5例癌症,包括2例PTC和3例肿瘤细胞甲状腺癌。值得注意的是,AUS-N结节的恶性率(52%)明显高于AUS-O结节(15%)(P = .002):结论:在小儿AUS甲状腺结节中,AUS-N结节的恶性风险明显高于AUS-O结节。这些发现可指导临床进行更适当的分诊,并/或改善儿科甲状腺AUS结节患者的治疗。
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来源期刊
Cancer Cytopathology
Cancer Cytopathology 医学-病理学
CiteScore
7.00
自引率
17.60%
发文量
130
审稿时长
1 months
期刊介绍: Cancer Cytopathology provides a unique forum for interaction and dissemination of original research and educational information relevant to the practice of cytopathology and its related oncologic disciplines. The journal strives to have a positive effect on cancer prevention, early detection, diagnosis, and cure by the publication of high-quality content. The mission of Cancer Cytopathology is to present and inform readers of new applications, technological advances, cutting-edge research, novel applications of molecular techniques, and relevant review articles related to cytopathology.
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