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本文引用的文献

1
Expanding the Spectrum of Non-V600E Mutations in Thyroid Nodules: Evidence-Based Data from a Tertiary Referral Centre.扩大甲状腺结节中非 V600E 突变谱:来自三级转诊中心的循证数据。
Int J Mol Sci. 2023 Feb 17;24(4):4057. doi: 10.3390/ijms24044057.
2
Effects of BRAF V600E and NRAS mutational status on the progression-free survival and clinicopathological characteristics of patients with melanoma.BRAF V600E和NRAS突变状态对黑色素瘤患者无进展生存期及临床病理特征的影响
Oncol Lett. 2022 Nov 24;25(1):27. doi: 10.3892/ol.2022.13613. eCollection 2023 Jan.
3
Induction of the BRAFV600E Mutation in Thyroid Cells Leads to Frequent Hypermethylation.甲状腺细胞中BRAFV600E突变的诱导导致频繁的高甲基化。
Clin Exp Otorhinolaryngol. 2022 Aug;15(3):273-282. doi: 10.21053/ceo.2022.00206. Epub 2022 May 4.
4
BRAF V600E mutation is associated with aggressive features in papillary thyroid carcinomas ≤ 1.5 cm.BRAF V600E 突变与 ≤ 1.5 cm 的甲状腺乳头状癌的侵袭性特征相关。
J Otolaryngol Head Neck Surg. 2021 Nov 6;50(1):63. doi: 10.1186/s40463-021-00543-9.
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BRAF V600E mutation in papillary thyroid carcinoma: it's relation to clinical features and oncologic outcomes in a single cancer centre experience.甲状腺乳头状癌中的BRAF V600E突变:单癌症中心经验中其与临床特征及肿瘤学结局的关系
Endocr Connect. 2021 Nov 25;10(12):1531-1537. doi: 10.1530/EC-21-0410.
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Kinase-inhibitors for iodine-refractory differentiated thyroid cancer: still far from a structured therapeutic algorithm.用于碘难治性分化型甲状腺癌的激酶抑制剂:仍远未形成结构化的治疗方案。
Crit Rev Oncol Hematol. 2021 Jun;162:103353. doi: 10.1016/j.critrevonc.2021.103353. Epub 2021 May 14.
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Prevalence of mutation in Asian series of papillary thyroid carcinoma-a contemporary systematic review.亚洲乳头状甲状腺癌系列中突变的患病率——一项当代系统评价
Gland Surg. 2020 Oct;9(5):1878-1900. doi: 10.21037/gs-20-430.
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Update on Fundamental Mechanisms of Thyroid Cancer.甲状腺癌基础机制的最新研究进展。
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9
Combined quantitation of HMGA2 mRNA, microRNAs, and mitochondrial-DNA content enables the identification and typing of thyroid tumors in fine-needle aspiration smears.联合定量分析 HMGA2 mRNA、microRNAs 和线粒体 DNA 含量可用于鉴定和分型细针抽吸涂片的甲状腺肿瘤。
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NCCN Guidelines Insights: Thyroid Carcinoma, Version 2.2018.NCCN 指南解读:甲状腺癌,第 2.2018 版。
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甲状腺乳头状癌患者固定玻片标本细针穿刺细胞学检查中的BRAF突变分析

BRAF Mutation Analysis in Fine-Needle Aspiration Cytology of Fixed Slide Specimens in Patients with Papillary Thyroid Carcinoma.

作者信息

Cheraghi Sara, Honardoost Maryam, Abdolmaleki Fereshteh, E Khamseh Mohammad

机构信息

Endocrine Research Center, Institute of Endocrinology and Metabolism, Iran University of Medical Sciences, Tehran, Iran.

出版信息

Med J Islam Repub Iran. 2024 Jul 22;38:83. doi: 10.47176/mjiri.38.83. eCollection 2024.

DOI:10.47176/mjiri.38.83
PMID:39678775
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11644031/
Abstract

BACKGROUND

Papillary thyroid carcinoma is the most frequent type of thyroid cancer. The BRAF mutation is associated with tumor progression. We explored the utility of the BRAF molecular testing on fine needle aspiration fixed specimens of patients with confirmed diagnoses of papillary thyroid carcinoma.

METHODS

Fixed thyroid cytology slide specimens of 19 patients with Bethesda II to VI reports were used to detect BRAF mutation by pyrosequencing of extracted DNA.

RESULTS

BRAF mutation was detected in 25% of the specimens with Bethesda category III and IV nodules and in 73% of the nodules with Bethesda category V and VI.

CONCLUSION

BRAF mutation analysis can be performed on fixed fine needle aspiration cytology specimens. Although the frequency of the mutation is higher in specimens with higher Bethesda category scores, it could support clinical decision-making in thyroid nodules with intermediate Bethesda category scores.

摘要

背景

乳头状甲状腺癌是最常见的甲状腺癌类型。BRAF突变与肿瘤进展相关。我们探讨了BRAF分子检测在确诊为乳头状甲状腺癌患者的细针穿刺固定标本中的应用价值。

方法

对19例具有贝塞斯达II至VI类报告的甲状腺细胞固定涂片标本,通过对提取的DNA进行焦磷酸测序来检测BRAF突变。

结果

在贝塞斯达III类和IV类结节的标本中,25%检测到BRAF突变;在贝塞斯达V类和VI类结节中,73%检测到BRAF突变。

结论

BRAF突变分析可在细针穿刺固定细胞学标本上进行。虽然在贝塞斯达分类评分较高的标本中突变频率更高,但它可为贝塞斯达分类评分中等的甲状腺结节的临床决策提供支持。