超越细胞学的桥本甲状腺炎:细胞学、激素、血清学和放射学表现之间的相关性。

IF 1.7 Q4 ENDOCRINOLOGY & METABOLISM Journal of Thyroid Research Pub Date : 2023-01-01 DOI:10.1155/2023/5707120
Sayed Ali Almahari, Reem Maki, Noor Al Teraifi, Safa Alshaikh, Nisha Chandran, Husain Taha
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引用次数: 1

摘要

桥本甲状腺炎是甲状腺慢性炎症最常见的原因。超声是检测方式,细针穿刺是诊断的金标准方法。血清学指标,如抗甲状腺过氧化物酶抗体(TPO)和抗甲状腺球蛋白抗体(TG),通常升高。目的:主要目的是评估桥本甲状腺炎背景下肿瘤的发生率。我们的第二个目标是识别桥本甲状腺炎的不同超声表现,重点关注其结节和局灶模式,并测量ACR TIRAD系统(2017)在桥本甲状腺炎患者解释时的敏感性。方法:单中心回顾性横断面研究。我们研究了2013年1月至2019年12月期间细胞学诊断为桥本甲状腺炎的137例病例。收集的数据使用SPSS(第26版)进行分析,超声检查由一位委员会认证的放射科医生进行审查。分别使用ACR甲状腺成像和数据系统2017 (ACR TI-RADs 2017)和Bethesda甲状腺细胞学报告系统2017 (BSRTC 2017)报告超声和细胞学。结果:患者平均年龄44.66岁,男女比例为9:1。血清学上,抗tg高22例(38%),抗tpo阳性60例。组织学诊断为甲状腺乳头状癌11例(8%),滤泡腺瘤1例(0.7%)。超声检查50%为弥漫性,其中13%为微结节。32.2%为大结节,17.7%为局灶性结节。ACR TIRAD系统(2017)对45个结节进行了解释,其中22.2%为TR2, 26.6%为TR3, 17.7%为TR4, 33.3%为TR5。结论:桥本甲状腺炎是发生甲状腺肿瘤的危险因素,需要对所研究的细胞学资料进行正确的评估,并与临床和放射学特征进行联系。认识桥本甲状腺炎的不同类型及其不同的表现对甲状腺超声成像的执行和解释具有重要意义。微钙化是区分PTC与结节型桥本甲状腺炎最敏感的指标。TIRAD系统(2017)是风险分层的有用工具;然而,由于桥本甲状腺炎的超声表现多变,可能会造成不必要的FNA研究。桥本甲状腺炎患者改良的TIRAD系统对于减轻这种混淆很重要。最后,抗tpo是检测桥本甲状腺炎的敏感标志物,可为今后新诊断病例提供参考。
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Hashimoto Thyroiditis beyond Cytology: A Correlation between Cytological, Hormonal, Serological, and Radiological Findings.

Introduction: Hashimoto thyroiditis is the most common cause of chronic inflammation of the thyroid gland. Ultrasound is the modality for detection, while fine needle aspiration is the gold standard method for diagnosis. Serologic markers, such as antithyroidal peroxidase antibody (TPO) and antithyroglobulin antibody (TG), are usually elevated.

Aim: The main objective is to appraise the incidence of neoplasms on a background of Hashimoto thyroiditis. Our second objective is to recognize the different sonographic appearances of Hashimoto thyroiditis, to focus on its nodular and focal patterns, and to measure the sensitivity of the ACR TIRAD system (2017) when interpreted on patients with Hashimoto thyroiditis.

Methods: A single-center retrospective cross-sectional study. We studied 137 cases diagnosed cytologically as Hashimoto thyroiditis from January 2013-December 2019. The data collected were analyzed using SPSS (26th edition), and ultrasounds were reviewed by a single board-certified radiologist. The ACR thyroid imaging and Data System 2017 (ACR TI-RADs 2017) and the Bethesda System for reporting thyroid cytology 2017 (BSRTC 2017) were used for reporting ultrasound and cytology, respectively.

Results: The mean age was 44.66 years and the female : male was 9 : 1. Serologically, anti-Tg was high in 22 cases (38%), while anti-TPO was positive in all of the 60 cases studied. Histologically, 11 cases were diagnosed with papillary thyroid carcinoma (8%) and a single case with follicular adenoma (0.7%). Ultrasonographically, 50% of the cases showed diffuse pattern, in which 13% of them showed micronodules. 32.2% were macronodular, and 17.7% were a focal nodular pattern. 45 nodules were interpreted with the ACR TIRAD system (2017), in which 22.2% were TR2, 26.6% were TR3, 17.7% were TR4, and 33.3% were TR5.

Conclusion: Hashimoto thyroiditis is a risk factor for developing thyroid neoplasms, which necessitate a proper assessment of the cytological material studied and a correlation with the clinical and radiological features. Recognizing the different types of Hashimoto thyroiditis and its variable appearances is significantly important in performing and interpreting thyroid ultrasound imaging. Microcalcification is the most sensitive parameter to discriminate between PTC and nodular type of Hashimoto thyroiditis. The TIRAD system (2017) is a useful tool for risk stratification; however, it might create unnecessary FNA studies in the setting of Hashimoto thyroiditis because of its variable appearances on ultrasound. A modified TIRAD system for patients with Hashimoto thyroiditis is important to alleviate this confusion. Finally, anti-TPO is a sensitive marker for detecting Hashimoto thyroiditis, which could be used for future referencing of newly diagnosed cases.

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来源期刊
Journal of Thyroid Research
Journal of Thyroid Research ENDOCRINOLOGY & METABOLISM-
CiteScore
4.40
自引率
0.00%
发文量
10
审稿时长
17 weeks
期刊最新文献
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