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Diagnostic utility of BRAFV600E mutation testing in thyroid nodules in elderly patients

机译:BRAFV600E突变检测在老年甲状腺结节中的诊断价值

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摘要

BackgroundThyroid cancer is a rare disease characterized by the subtle appearance of a nodule. Fine-needle cytology (FNC) is the first diagnostic procedure used to distinguish a benign from a malignant nodule. However, FNC yields inconclusive results in about 20% of cases. BRAFV600E mutation is the most frequent genetic alteration in papillary thyroid carcinoma (PTC); its high prevalence makes this oncogene a useful marker to refine inconclusive FNC results. However, the prevalence of the BRAFV600E mutation depends on detection methods, geographical factors, and age. The aim of this study is to determine the prevalence of BRAFV600E mutation and its utility as a diagnostic tool in elderly subjects.
机译:背景甲状腺癌是一种罕见的疾病,其特征在于结节的微妙外观。细针细胞学检查(FNC)是用于区分良性结节和恶性结节的首个诊断程序。但是,在大约20%的情况下,FNC的结果尚无定论。 BRAF V600E 突变是乳头状甲状腺癌(PTC)中最常见的基因改变;其高患病率使该癌基因成为改善不确定FNC结果的有用标记。但是,BRAF V600E 突变的患病率取决于检测方法,地理因素和年龄。这项研究的目的是确定BRAF V600E 突变的患病率及其在老年受试者中作为诊断工具的实用性。

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