甲状腺贝塞斯达细胞病理学报告系统》第 2 版与第 3 版之间过渡地带的甲状腺贝塞斯达第 III 类(AUS)的综合方法:亚分类、核评分等。

IF 11.3 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Endocrine Pathology Pub Date : 2024-03-01 Epub Date: 2024-01-27 DOI:10.1007/s12022-024-09797-1
Merve Bagıs, Nuray Can, Necdet Sut, Ebru Tastekin, Ezgi Genc Erdogan, Buket Yilmaz Bulbul, Yavuz Atakan Sezer, Osman Kula, Elif Mercan Demirtas, Inci Usta
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引用次数: 0

摘要

贝塞斯达甲状腺细胞病理学报告系统》(The Bethesda System for Reporting Thyroid Cytopathology,TBSRTC)中的贝塞斯达第三类:意义未定的不典型细胞(atypia of undetermined significance,AUS)在观察者之间存在显著差异。因此,最近出版的第三版《贝塞斯达甲状腺细胞病理报告系统》提出了 AUS 的分类,包括 AUS "核 "和 AUS "其他"。本研究调查了核特征/结构特征/核评分(NS)(三层)/亚类和亚组对甲状腺细针抽吸术(FNA)中恶性肿瘤风险(ROM)的影响。共对 6940 例 FNA 进行了评估。其中1224例(17.6%)被诊断为AUS,240例患者(260个结节的初始FNA和240例甲状腺切除术)被纳入其中。根据 TBSRTC 第 2 版和第 3 版定义了亚类和亚组。组织学诊断组包括非肿瘤性疾病、良性肿瘤、低风险肿瘤和恶性肿瘤。总体而言,ROM 为 30.7%。核重叠(35.5%)、核成型(56.9%)、轮廓不规则(42.1%)、核沟(74.1%)、染色质清晰(49.4%)和染色质边缘化(57.7%)的FNA的ROM明显更高,这些特征是恶性肿瘤的独立重要预测因素。带有 NS3 的 FNA 的 ROM 明显更高(64.2%)。三维组在恶性肿瘤中的发生率明显更高(35.7%)。AUS-核亚类(48.2%)和AUS-核与结构亚类(38.3%)的ROM明显更高。AUS-核1亚组的ROM最高(65.2%)。包括澳大-核和澳大-核及建筑亚类的 "高风险组 "的 ROM 明显高于包括其他亚类的 "低风险组"(42.0%vs 13.9%)。总之,亚分类可能不是终点,根据严格的标准进行核评分和建筑模式评估可为重塑 TBSRTC 类别提供数据。
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A Comprehensive Approach to the Thyroid Bethesda Category III (AUS) in the Transition Zone Between 2nd Edition and 3rd Edition of The Bethesda System for Reporting Thyroid Cytopathology: Subcategorization, Nuclear Scoring, and More.

Significant interobserver variabilities exist for Bethesda category III: atypia of undetermined significance (AUS) of The Bethesda System for Reporting Thyroid Cytopathology (TBSRTC). Thus, subcategorization of AUS including AUS "nuclear" and AUS "other" is proposed in the recent 3rd edition of TBSRTC. This study investigated the impact of the nuclear features/architectural features/nuclear score (NS) (3-tiered)/subcategories and subgroups on risk of malignancy (ROM) in thyroid fine-needle aspirations (FNA). 6940 FNAs were evaluated. 1224 (17.6%) cases diagnosed as AUS were reviewed, and 240 patients (initial FNAs of 260 nodules and 240 thyroidectomies) were included. Subcategories and subgroups were defined according to TBSRTC 2nd and 3rd editions. Histological diagnostic groups included nonneoplastic disease, benign neoplasm, low-risk neoplasm, and malignant neoplasm. Overall, ROM was 30.7%. ROM was significantly higher in FNAs with nuclear overlapping (35.5%), nuclear molding (56.9%), irregular contours (42.1%), nuclear grooves (74.1%), chromatin clearing (49.4%), and chromatin margination (57.7%), and these features were independent significant predictors for malignancy. FNAs with NS3 had significantly higher ROM (64.2%). Three-dimensional groups were significantly more frequent in malignant neoplasms (35.7%). ROM was significantly higher in AUS-nuclear subcategory (48.2%) and in AUS-nuclear and architectural subcategory (38.3%). The highest ROM was detected in AUS-nuclear1 subgroup (65.2%). ROM was significantly higher in the group including AUS-nuclear and AUS-nuclear and architectural subcategories, namely "high-risk group" than the group including other subcategories, namely "low-risk group" (42.0%vs 13.9%). In conclusion, subcategorization may not be the end point, and nuclear scoring and evaluation of architectural patterns according to strict criteria may provide data for remodeling of TBSRTC categories.

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来源期刊
Endocrine Pathology
Endocrine Pathology 医学-病理学
CiteScore
12.30
自引率
20.50%
发文量
41
审稿时长
>12 weeks
期刊介绍: Endocrine Pathology publishes original articles on clinical and basic aspects of endocrine disorders. Work with animals or in vitro techniques is acceptable if it is relevant to human normal or abnormal endocrinology. Manuscripts will be considered for publication in the form of original articles, case reports, clinical case presentations, reviews, and descriptions of techniques. Submission of a paper implies that it reports unpublished work, except in abstract form, and is not being submitted simultaneously to another publication. Accepted manuscripts become the sole property of Endocrine Pathology and may not be published elsewhere without written consent from the publisher. All articles are subject to review by experienced referees. The Editors and Editorial Board judge manuscripts suitable for publication, and decisions by the Editors are final.
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