穿刺活检、ct及BRAFV600E基因联合检测对甲状腺乳头状癌具有较高的诊断价值。

IF 2.3 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM
Peizhi Fan, Zhaoyi Wu, Zhecheng Li, Huiting Ouyang, Jianing Yi, Jie Yu
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引用次数: 0

摘要

目的:探讨超声引导下细针穿刺活检(US-FNAB)、CT及BRAFV600E联合诊断甲状腺乳头状癌(PTC)的临床价值。对象和方法:将300例甲状腺结节患者分为PTC组(n = 184)和结节性甲状腺肿组(n = 116)。分析US-FNAB、CT、BRAFV600E基因突变的阳性检出率及其与肿瘤数量、肿瘤直径、淋巴转移、包膜侵袭、肿瘤淋巴结转移(TNM)分期的关系,并通过受试者工作特征(ROC)曲线分析其对PTC的诊断价值。采用MEDCALC软件比较多个ROC曲线下面积(auc)。结果:PTC组US-FNAB、CT和BRAFV600E基因突变阳性检出率分别为78.80%、72.28%和83.15%,NG组为30.17%、27.59%和9.48%;PTC组阴性检出率分别为21.20%、27.72%和16.85%,NG组为69.82%、72.41%和90.52%。PTC患者US-FNAB和BRAFV600E基因阳性突变与TNM分期相关CT阳性和BRAFV600E基因突变与淋巴转移有关。US-FNAB (AUC: 0.743,敏感性:78.80%,特异性:69.83%)、CT (AUC: 0.723,敏感性:77.28%,特异性:72.41%)和BRAFV600E (AUC: 0.868,敏感性:83.15%,特异性:90.52%)基因检测有助于PTC的诊断,其综合诊断价值(AUC: 0.938,敏感性:78.26%,特异性:96.55%)超过单独检测。结论:US-FNAB、CT和BRAFV600E基因检测有助于PTC的诊断,且三者联合检测对PTC的诊断价值高于单项检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The combined detection of aspiration biopsy, computed tomography and BRAFV600E gene has high diagnostic value for papillary thyroid carcinoma.

The combined detection of aspiration biopsy, computed tomography and BRAFV600E gene has high diagnostic value for papillary thyroid carcinoma.

The combined detection of aspiration biopsy, computed tomography and BRAFV600E gene has high diagnostic value for papillary thyroid carcinoma.

Objective: This study investigated the clinical value of ultrasound-guided fine-needle aspiration biopsy (US-FNAB), computed tomography (CT) and BRAFV600E combination for papillary thyroid carcinoma (PTC) diagnosis.

Subjects and methods: A total of 300 patients with thyroid nodules were assigned to the PTC group (n = 184) and the nodular goiter (NG) group (n = 116). The positive detection rates of US-FNAB, CT and BRAFV600E gene mutation and their relationship with tumor number, tumor diameter, lymphatic metastasis, capsule invasion and tumor-node-metastasis (TNM) staging were analyzed, with their diagnostic value for PTC analyzed by the receiver operating characteristic (ROC) curve. The area under multiple ROC curves (AUCs) were compared using MEDCALC software.

Results: The positive detection rates of US-FNAB, CT and BRAFV600E gene mutation were 78.80%, 72.28% and 83.15% in the PTC group, and 30.17%, 27.59% and 9.48% in the NG group, while the negative detection rates were 21.20%, 27.72% and 16.85% in the PTC group, and 69.82%, 72.41% and 90.52% in the NG group. Positive US-FNAB and BRAFV600E gene mutation in PTC patients related to TNM staging. Positive CT and BRAFV600E gene mutation linked to lymphatic metastasis. US-FNAB (AUC: 0.743, sensitivity: 78.80%, specificity: 69.83%), CT (AUC: 0.723, sensitivity: 77.28%, specificity: 72.41%) and BRAFV600E (AUC: 0.868, sensitivity: 83.15%, specificity: 90.52%) gene detections helped PTC diagnosis, with their combined diagnostic value (AUC: 0.938, sensitivity: 78.26%, specificity: 96.55%) surpassing that of them alone.

Conclusion: US-FNAB, CT and BRAFV600E gene tests helped PTC diagnosis, and their combined detection had higher diagnostic value for PTC than their single detection.

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来源期刊
Archives of Endocrinology Metabolism
Archives of Endocrinology Metabolism Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.90
自引率
5.90%
发文量
107
审稿时长
7 weeks
期刊介绍: The Archives of Endocrinology and Metabolism - AE&M – is the official journal of the Brazilian Society of Endocrinology and Metabolism - SBEM, which is affiliated with the Brazilian Medical Association. Edited since 1951, the AE&M aims at publishing articles on scientific themes in the basic translational and clinical area of Endocrinology and Metabolism. The printed version AE&M is published in 6 issues/year. The full electronic issue is open access in the SciELO - Scientific Electronic Library Online e at the AE&M site: www.aem-sbem.com. From volume 59 on, the name was changed to Archives of Endocrinology and Metabolism, and it became mandatory for manuscripts to be submitted in English for the online issue. However, for the printed issue it is still optional for the articles to be sent in English or Portuguese. The journal is published six times a year, with one issue every two months.
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