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超声引导锁骨上淋巴结细针抽吸物中 EGFR 基因突变的可靠检测:一项具有诊断性能分析的队列研究。

Reliable EGFR mutation testing in ultrasound-guided supraclavicular lymph node fine-needle aspirates: a cohort study with diagnostic performance analysis.

机构信息

Radiology Department , Nottingham University Hospitals NHS Trust, Queen's Medical Centre , Nottingham, Nottinghamshire , UK.

Histopathology Department , Nottingham University Hospitals NHS Trust, Queen's Medical Centre , Nottingham, Nottinghamshire , UK.

出版信息

BMJ Open Respir Res. 2015 Jul 1;2(1):e000075. doi: 10.1136/bmjresp-2014-000075. eCollection 2015.

Abstract

INTRODUCTION

15-30% of patients with lung cancer will have supraclavicular and cervical lymphadenopathy (SCLN). Ultrasound (US)-guided fine-needle aspiration (FNA) cytology is regarded as an effective diagnostic tool in small size lymph nodes (LNs) and impalpable positron emission tomography detected nodes. We evaluated our diagnostic service performance in relation to the adequacy of samples for epidermal growth factor receptor (EGFR) mutation.

METHODS

Retrospective data analysis from electronic records, searching for all suspected lung cancer referrals that underwent US of the neck±FNA, over a continuous period of 4 years.

RESULTS

Of 306 cases with suspected lung cancer referred to our department for US FNA of SCLN, 228 patients underwent the procedure. Of the remaining 78 patients, LNs were not detected in 52 cases and appeared benign in 26. Cytological diagnosis was established in 171 patients (75%) for treatment decisions without further investigations. The remaining 57 patients had further investigations; 45 reconfirmed the US-guided FNA diagnosis. The average LN size was 12.9 mm, and positive cytology was obtained in LNs ranging from 3 to 45 mm. Of 57 adenocarcinoma cases, 34 were tested for EGFR confirming 4 positive, 25 negative and 5 insufficient samples. No complications were recorded.

CONCLUSIONS

US-guided FNA of SCLN remains an important diagnostic tool in lung cancer. Adequate tissue can be obtained for reliable diagnosis from LNs and for EGFR mutational analysis, without the need for more invasive and expensive investigations in more than 80% of cases.

摘要

简介

15%-30%的肺癌患者会出现锁骨上和颈部淋巴结病(SCLN)。超声(US)引导下细针抽吸(FNA)细胞学检查被认为是一种有效的诊断工具,适用于小尺寸淋巴结(LNs)和触诊阴性的正电子发射断层扫描(PET)检测到的淋巴结。我们评估了我们的诊断服务性能,与表皮生长因子受体(EGFR)突变的样本充足性有关。

方法

回顾性电子病历数据分析,搜索 4 年来所有疑似肺癌转诊患者的颈部 US±FNA。

结果

306 例疑似肺癌患者中,228 例接受了 US 引导下的 SCLN FNA。在其余 78 例患者中,52 例未检出 LNs,26 例 LNs 表现为良性。171 例患者(75%)进行了细胞学诊断,为治疗决策提供了依据,无需进一步检查。其余 57 例患者进行了进一步检查;45 例患者再次确认了 US 引导下 FNA 的诊断。平均 LN 大小为 12.9mm,阳性细胞学结果来自 3-45mm 的 LN。57 例腺癌患者中,有 34 例进行了 EGFR 检测,其中 4 例为阳性,25 例为阴性,5 例为样本不足。未记录到任何并发症。

结论

US 引导下的 SCLN FNA 仍然是肺癌的重要诊断工具。从 LN 中可以获得足够的组织进行可靠的诊断和 EGFR 突变分析,无需对 80%以上的病例进行更具侵袭性和昂贵的检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c730/4488608/be4b0fd23848/bmjresp2014000075f01.jpg

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