Thyroid cytology in pediatric patients: a single-center study from 2015 to 2023-is there a necessity for distinct treatment approaches for patients with and without autoimmune thyroiditis?

IF 3.4 3区 医学 Q1 PATHOLOGY
Monika Kujdowicz, Dominika Januś, Jan Radliński, Aleksandra Kiszka-Wiłkojć, Anna Taczanowska-Niemczuk, Damian Młynarski, Wojciech Górecki, Jerzy B Starzyk, Dariusz Adamek
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Abstract

The management of thyroid nodules is guided by the cytological classification provided by The Bethesda System for Reporting Thyroid Cytology. Notably, the biology of thyroid tumors in pediatric patients differs from that in adults, and there is limited research focused on pediatric cases. This study aimed to assess the effectiveness of the Bethesda system in pediatric patients treated at the largest tertiary pediatric thyroid center in Poland between 2015 and 2023. A retrospective analysis was conducted on 566 patients with thyroid nodules, of whom 555 underwent fine-needle aspiration biopsy (FNAB). A total of 217 patients underwent thyroid surgery. Of these, 206 had previously undergone FNAB with cytological evaluation at our center, while 11 patients underwent thyroid surgery due to a RET mutation or the need for an extended procedure. The initial FNAB results showed distribution across Bethesda categories as follows: 7.6% for category I, 54.6% for category II, 20.9% for category III, 4.1% for category IV, 7.6% for category V, and 5.6% for category VI. Among patients who underwent surgery, the distribution of Bethesda categories I through VI was 2.9%, 25.2%, 29.1%, 8.3%, 19.4%, and 15%, respectively. The risk of malignancy (ROM) from the initial FNAB was estimated at 33.3%, 11.5%, 22.2%, 4.8%, 84.4%, and 96.8% for Bethesda categories I through VI, respectively. In patients with autoimmune thyroiditis (AIT), the ROM was higher than in non-AIT patients for Bethesda categories I through IV, while it was lower in category VI. The sensitivity for detecting non-benign neoplasms across Bethesda categories III through VI was approximately 86% in both AIT and non-AIT patients. However, for papillary thyroid carcinoma, sensitivity in Bethesda categories V and VI was 86% in non-AIT patients but decreased to 61.5% in AIT patients. These findings emphasize the importance of considering surgical intervention in pediatric patients with Bethesda III-VI cytology, particularly in those with AIT.

儿科患者的甲状腺细胞学检查:2015年至2023年的单中心研究--是否有必要对自身免疫性甲状腺炎患者和非自身免疫性甲状腺炎患者采取不同的治疗方法?
甲状腺结节的治疗以《贝塞斯达甲状腺细胞学报告系统》(The Bethesda System for Reporting Thyroid Cytology)提供的细胞学分类为指导。值得注意的是,儿科甲状腺肿瘤的生物学特性与成人不同,而针对儿科病例的研究也很有限。本研究旨在评估贝塞斯达系统对2015年至2023年期间在波兰最大的三级甲状腺中心接受治疗的儿科患者的有效性。研究对566名甲状腺结节患者进行了回顾性分析,其中555人接受了细针穿刺活检(FNAB)。共有 217 名患者接受了甲状腺手术。其中,206名患者曾在本中心接受过FNAB和细胞学评估,11名患者因RET突变或需要延长手术时间而接受了甲状腺手术。最初的FNAB结果显示,贝塞斯达分类的分布情况如下:I类占7.6%,II类占54.6%,III类占20.9%,IV类占4.1%,V类占7.6%,VI类占5.6%。在接受手术的患者中,贝塞斯达分类 I 至 VI 的分布比例分别为 2.9%、25.2%、29.1%、8.3%、19.4% 和 15%。据估计,Bethesda I至VI类患者初次FNAB的恶性肿瘤风险(ROM)分别为33.3%、11.5%、22.2%、4.8%、84.4%和96.8%。在自身免疫性甲状腺炎(AIT)患者中,贝塞斯达分类Ⅰ至Ⅳ的ROM高于非AIT患者,而分类Ⅵ的ROM则低于非AIT患者。无论是自身免疫性甲状腺炎患者还是非自身免疫性甲状腺炎患者,在贝塞斯达分类 III 至 VI 中检测非良性肿瘤的灵敏度均约为 86%。但是,对于甲状腺乳头状癌,非 AIT 患者对 Bethesda V 类和 VI 类的敏感度为 86%,而 AIT 患者则降至 61.5%。这些发现强调了考虑对Bethesda III-VI细胞学检查的儿科患者,尤其是AIT患者进行手术干预的重要性。
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
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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