首页|超声引导下细针穿刺细胞学、鼠类肉瘤病毒癌基因同源物B V600E基因突变单独及联合检测对甲状腺癌的诊断价值

超声引导下细针穿刺细胞学、鼠类肉瘤病毒癌基因同源物B V600E基因突变单独及联合检测对甲状腺癌的诊断价值

Diagnostic value of ultrasound-guided fine-needle aspiration cytology,v-raf murine sarcoma viral oncogene homolog B V600E gene mutation single and combined detection for thyroid cancer

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目的 探讨超声引导下细针穿刺(FNA)细胞学、鼠类肉瘤病毒癌基因同源物B(BRAF)V600E基因突变单独及联合检测对甲状腺癌的诊断价值.方法 选取127例甲状腺结节患者,均接受超声引导下FNA细胞学、BRAF V600E基因突变检测,以病理检查结果为金标准,评估FNA细胞学、BRAF V600E基因突变单独及联合检测对甲状腺癌的诊断价值;采用Kappa检验评估FNA细胞学、BRAF V600E基因突变单独及联合检测诊断甲状腺癌的结果与病理检查结果的一致性.结果 FNA细胞学、BRAF V600E基因突变联合检测诊断甲状腺癌的灵敏度为98.06%,特异度为100%,准确度为98.43%,阳性预测值为100%,阴性预测值为92.31%,均高于二者单独检测.FNA细胞学、BRAF V600E基因突变联合检测诊断甲状腺癌的结果与病理检查结果的一致性极高(Kappa=0.950),高于BRAF V600E基因突变(Kappa=0.877)和FNA细胞学(Kappa=0.772)单独检测.病理检查结果显示,阳性(甲状腺癌)103例,阴性24例,分别作为恶性组和良性组.恶性组患者FNA细胞学检测评分明显高于良性组,BRAF V600E基因突变检测CT值明显低于良性组,差异均有统计学意义(P<0.01).结论 FNA细胞学、BRAF V600E基因突变联合检测对甲状腺癌具有较高的诊断价值.
Objective To explore the diagnostic value of ultrasound-guided fine-needle aspiration(FNA)cytology,v-raf murine sarcoma viral oncogene homolog B(BRAF)V600E gene mutation single and combined detection for thyroid cancer.Method A total of 127 patients with thyroid nodules were selected and underwent ultrasound-guided FNA cytol-ogy and BRAF V600E gene mutation detection.Pathological examination result was used as the gold standard,the diag-nostic value of FNA cytology and BRAF V600E gene mutation single and combined detection for thyroid cancer were evaluated.The Kappa test was used to evaluate the consistency between the results of FNA cytology and BRAF V600E gene mutation single and combined detection for the diagnosis of thyroid cancer and the pathological examination results.Result The sensitivity of FNA cytology and BRAF V600E gene mutation combined detection for the diagnosis of thy-roid cancer was 98.06%,specificity was 100%,accuracy was 98.43%,positive predictive value was 100%,and negative predictive value was 92.31%,which were higher than those of the single detection.The consistency between the results of FNA cytology and BRAF V600E gene mutation combined detection in diagnosing thyroid cancer and pathological exami-nation was extremely high(Kappa=0.950),which was higher than those of BRAF V600E gene mutation detection(Kap-pa=0.877)and FNA cytology detection(Kappa=0.772),respectively.Pathological examination results showed that 103 cases were positive(thyroid cancer)and 24 cases were negative,which were classified as malignant group and benign group,respectively.The FNA cytology score of malignant group was significantly higher than that of benign group,and the CT value of BRAF V600E gene mutation detection was significantly lower than that of benign group,the differences were statistically significant(P<0.01).Conclusion The FNA cytology and BRAF V600E gene mutation combined detec-tion has high diagnostic value for thyroid cancer.

thyroid cancerfine-needle aspiration cytologyv-raf murine sarcoma viral oncogene homolog Bgene mutation

王明军、薛源、乔楠、乔乐乐、刘九洲、任宁、程维刚

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河南科技大学临床医学院/河南科技大学第一附属医院甲状腺头颈肿瘤外科,河南 洛阳 471003

甲状腺癌 细针穿刺细胞学 鼠类肉瘤病毒癌基因同源物B 基因突变

2024

癌症进展
中国医学科学院,北京协和医学院

癌症进展

影响因子:1.004
ISSN:1672-1535
年,卷(期):2024.22(17)