Diagnostic performance of ACR-TIRADS for thyroid nodule risk stratification in pediatric patients.

IF 2.9 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Anita Lavarda Scheinpflug, Leonardo Barbi Walter, Laura Marmitt, Rafael Selbach Scheffel, Mariangela Gheller Friedrich, Mauricio Farenzena, Carlo Sasso Faccin, Marcia Silveira Graudenz, José Miguel Dora, Ana Luiza Maia, Andre Borsatto Zanella
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引用次数: 0

Abstract

Purpose: The American College of Radiology Thyroid Imaging Reporting and Data System (ACR-TIRADS) is a widely used ultrasonographic risk-stratification system for thyroid nodules in adults and its use has been increasingly expanding in the pediatric population in recent years. Here, we evaluated the diagnostic performance of ACR-TIRADS in patients aged ≤ 18 years with thyroid nodules.

Methods: We performed a single-center retrospective cohort study of patients aged ≤ 18 years, followed by tertiary care for thyroid nodules. The ACR-TIRADS data were extracted from the image records by two radiologists with expertise in thyroid imaging. Malignancy rates were defined based on cytological examinations, histological diagnosis, or ultrasonographic follow-up concerning nodule characteristics and size.

Results: The cohort comprised 58 patients (65 nodules). The majority were female (70.7%), with a mean age of 14.0 ± 3.4 years and 27.5% had at least one risk factor for thyroid malignancy. The malignancy rate was 20.7% (N = 12). We could not reassess the ultrasound images of 9 patients; therefore, for this analysis, 49 patients (56 nodules) were included. The TIRADS nodule classifications were as follows: 8 TR1 (14.3%), 18 TR2 (32.1%), 15 TR3 (26.8%), 7 TR4 (12.5%), and 8 TR5 (14.3%). The ACR-TIRADS interobserver agreement was high, with a free marginal kappa of 0.86 [95% confidence interval (CI): 0.75, 0.97]. All TR1, TR2, and TR3 nodules were benign, and 8 cases of thyroid malignant neoplasm in the TR4 (N = 1) and TR5 (N = 7) groups resulted in malignancy rates of 14.3 and 87.5%, respectively. Remarkably, the TR5 nodules exhibited a positive predictive value of 87.5%, negative predictive value of 97.9%, sensitivity of 87.5%, and specificity of 97.9% for predicting malignancy. We did not identify a cutoff of nodule size for predicting malignancy - area under the receiver operating characteristic curve (AUC) of 0.58 (95% CI 0.38-0.80).

Conclusion: ACR-TIRADS effectively stratifies malignancy risk in pediatric thyroid nodules, with TR5 nodules showing particularly high malignancy risk. Clinical risk factors combined with ultrasound characteristics provide better malignancy prediction than nodule size alone in this population.

ACR-TIRADS对儿科患者甲状腺结节风险分层的诊断价值。
目的:美国放射学会甲状腺影像学报告与数据系统(ACR-TIRADS)是一种广泛应用于成人甲状腺结节的超声风险分层系统,近年来在儿科人群中的应用日益扩大。在这里,我们评估了ACR-TIRADS对年龄≤18岁甲状腺结节患者的诊断性能。方法:我们对年龄≤18岁的患者进行了一项单中心回顾性队列研究,随后进行了甲状腺结节的三级护理。ACR-TIRADS数据由两名具有甲状腺成像专业知识的放射科医生从图像记录中提取。恶性肿瘤的发生率是根据细胞学检查、组织学诊断或超声检查的结节特征和大小来确定的。结果:该队列包括58例患者(65例结节)。其中女性居多(70.7%),平均年龄14.0±3.4岁,27.5%至少有一种甲状腺恶性肿瘤危险因素。恶性肿瘤发生率为20.7% (N = 12)。9例患者超声图像不能再评价;因此,本分析纳入了49例患者(56个结节)。TIRADS结节分类如下:TR1型8例(14.3%)、TR2型18例(32.1%)、TR3型15例(26.8%)、TR4型7例(12.5%)、TR5型8例(14.3%)。ACR-TIRADS的观察者间一致性很高,自由边际kappa为0.86[95%置信区间(CI): 0.75, 0.97]。TR1、TR2、TR3组结节均为良性,其中TR4组(N = 1)、TR5组(N = 7)甲状腺恶性肿瘤8例,恶性率分别为14.3%、87.5%。值得注意的是,TR5结节预测恶性肿瘤的阳性预测值为87.5%,阴性预测值为97.9%,敏感性为87.5%,特异性为97.9%。我们没有发现预测恶性肿瘤的结节大小的截止值——接受者工作特征曲线(AUC)下的面积为0.58 (95% CI 0.38-0.80)。结论:ACR-TIRADS对儿童甲状腺结节的恶性风险进行了有效的分层,其中TR5结节的恶性风险特别高。在这一人群中,临床危险因素结合超声特征比单纯的结节大小提供更好的恶性肿瘤预测。
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来源期刊
Endocrine
Endocrine ENDOCRINOLOGY & METABOLISM-
CiteScore
6.50
自引率
5.40%
发文量
295
审稿时长
1.5 months
期刊介绍: Well-established as a major journal in today’s rapidly advancing experimental and clinical research areas, Endocrine publishes original articles devoted to basic (including molecular, cellular and physiological studies), translational and clinical research in all the different fields of endocrinology and metabolism. Articles will be accepted based on peer-reviews, priority, and editorial decision. Invited reviews, mini-reviews and viewpoints on relevant pathophysiological and clinical topics, as well as Editorials on articles appearing in the Journal, are published. Unsolicited Editorials will be evaluated by the editorial team. Outcomes of scientific meetings, as well as guidelines and position statements, may be submitted. The Journal also considers special feature articles in the field of endocrine genetics and epigenetics, as well as articles devoted to novel methods and techniques in endocrinology. Endocrine covers controversial, clinical endocrine issues. Meta-analyses on endocrine and metabolic topics are also accepted. Descriptions of single clinical cases and/or small patients studies are not published unless of exceptional interest. However, reports of novel imaging studies and endocrine side effects in single patients may be considered. Research letters and letters to the editor related or unrelated to recently published articles can be submitted. Endocrine covers leading topics in endocrinology such as neuroendocrinology, pituitary and hypothalamic peptides, thyroid physiological and clinical aspects, bone and mineral metabolism and osteoporosis, obesity, lipid and energy metabolism and food intake control, insulin, Type 1 and Type 2 diabetes, hormones of male and female reproduction, adrenal diseases pediatric and geriatric endocrinology, endocrine hypertension and endocrine oncology.
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