甲状腺细针穿刺细胞学检查联合BRAFV600E基因检测在ACR TR5微小结节术前诊断中的应用价值
DOI:
作者:
作者单位:

1.南京医科大学附属无锡人民医院超声科;2.南京医科大学附属无锡人民医院内分泌科;3.南京医科大学附属无锡人民医院甲乳外科

作者简介:

通讯作者:

中图分类号:

基金项目:

无锡市科技局指令性项目(N20192049)


The Value of Fine-needle Aspiration Biopsy Combined with BRAFV600E Gene Mutation Detection in Preoperative Diagnosis of ACR TR5 Micronodules
Author:
Affiliation:

Fund Project:

The project of Wuxi science and technology development fund(N20192049)

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    目的 评估甲状腺结节细针穿刺(fine-needle aspiration, FNA)细胞学检查联合BRAFV600E基因检测对直径≤5 mm,ACR评分为 TI-RADS 5的甲状腺微小结节良恶性的术前诊断价值及意义。方法 回顾性分析75例患者的96枚直径≤5 mm、ACR评分为 TR 5的甲状腺微小结节术前FNA细胞学检查和BRAFV600E基因检测结果,以手术病理为金标准,分析FNA细胞学检查、BRAFV600E基因突变检测以及两者联合对甲状腺微小结节良恶性的诊断价值。结果 FNA细胞学检查联合BRAFV600E基因突变检测的敏感性、准确性、特异性、阳性预测值、阴性预测值分别为95.0%、93.8%、91.7%、95.0%、91.7%,受试者工作特征(ROC)曲线下面积为0.933。FNA细胞学检查联合BRAFV600E基因突变检测的敏感性、准确性和ROC曲线下面积比较均高于单独FNA细胞学检查及BRAFV600E基因突变检测,差异有统计学意义(P<0.05)。结论 FNA细胞学检查联合BRAFV600E基因突变检测可以提高直径≤5 mm且评分为TR 5的甲状腺微小结节的术前诊断效能,减少漏诊的发生。同时对于直径≤5 mm的特殊位置以及多灶性的甲状腺微小结节FNA细胞学检查联合BRAFV600E基因突变检测可以在提高穿刺准确性的基础上,帮助患者争取治疗的最佳时期,确定最佳的手术方案。

    Abstract:

    Objective To evaluate the preoperative diagnosis value of fine-needle aspiration(FNA)cytological examination combined with the detection of BRAFV600E gene mutation in benign and malignant thyroid micronodules of ACR TI-RADS 5 with diameter≤5 mm . Methods The results of FNA cytological examination and BRAFV600E gene mutation detection in 75 patients with 96 thyroid nodules (TR 5 and diameter≤5 mm) before operation were retrospectively analysed. Postoperative pathological examination was regarded as the gold standard, the diagnostic performance of FNA cytological examination, BRAFV600E gene mutation detection and two methods combined in the differential diagnosis of benign and malignant thyroid micronodules was comparatively analyzed.?Results The sensitivity, specificity, accuracy, positive predictive value and negative predictive value of FNA cytological examination combined with the detection of BRAFV600E gene mutation were 95.0%、93.8%、91.7%、95.0%、91.7%,, the area under the receiver operating characteristic (ROC) curve was 0.933. The sensitivity、accuracy、negative predictive value and the area under the ROC curve of FNA cytological examination combined with the detection of BRAFV600E gene mutation was significantly higher than that of FNA cytological examination or BRAFV600E gene mutation detection alone(P<0.05). Conclusion FNA cytological examination combined with the detection of BRAFV600E gene mutation can improve the preoperative diagnosis efficiency of TR 5 thyroid micronodules with diameter≤5 mm , and can reduce the occurrence of missed diagnosis. FNA thyroid micronodules combined with the detection of BRAFV600E gene mutation can not only improve the puncture accuracy, but also help to strive for the best therapy period and to determine the best surgical plan for the special location and multifocal thyroid nodules with the diameter≤5 mm.

    参考文献
    相似文献
    引证文献
引用本文
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2020-05-31
  • 最后修改日期:2020-12-11
  • 录用日期:2021-09-01
  • 在线发布日期:
  • 出版日期: