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首页> 外文期刊>Cytopathology >Insulinoma-associated protein 1 expression in pancreatic neuroendocrine tumours in endoscopic ultrasound-guided fine-needle aspiration cytology: An analysis of 14 patients
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Insulinoma-associated protein 1 expression in pancreatic neuroendocrine tumours in endoscopic ultrasound-guided fine-needle aspiration cytology: An analysis of 14 patients

机译:胰岛素相关蛋白1内窥镜超声引导细针穿刺细胞学中胰腺神经内分泌肿瘤的表达:14例患者分析

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摘要

Background Insulinoma-associated protein 1 (INSM1) has been reported to be a useful marker for diagnosing pancreatic neuroendocrine tumours (PNETs). However, INSM1 expression in endoscopic ultrasound-guided fine needle aspiration cytology has not been examined. We evaluated INSM1 expression in the cytology of cases diagnosed with PNETs. Methods We immunocytochemically stained INSM1 and Ki-67 in 14 PNET cases, and according to the 2017 World Health Organisation criteria, seven PNET Grade 1 cases, four Grade 2 cases and three Grade 3/neuroendocrine carcinoma cases were identified. As a control for INSM1 and Ki-67 expression, we used cytological specimens from 15 cases of pancreatic ductal adenocarcinoma. Results In PNET cases, INSM1-expressing tumour cells were identified in all cytological specimens of PNET. The median INSM1 expression rate in Grade 1 cases was 49.8% (mean +/- standard deviation: 55.1 +/- 12.5%, min: 39.3%, max: 74.1%), and in Grade 2 and Grade 3/neuroendocrine carcinoma cases was 81.1% (mean +/- standard deviation: 77.6 +/- 18.6%, min: 50.3%, max: 100%). However, there was no correlation between INSM1 and Ki-67 expression (r = -0.15). The median expression rate in PNET cases was 64.3%, which was significantly higher than that in pancreatic ductal adenocarcinoma cases (P 0.0001). Conclusion INSM1 immunocytochemistry of cytological specimens obtained from endoscopic ultrasound-guided fine needle aspiration cytology can accurately diagnose PNETs; therefore, INSM1 could be an important diagnostic tool in assessing therapeutic strategies, including molecular-targeted therapy.
机译:背景技术胰胰岛素相关蛋白1(INSM1)已据报道是用于诊断胰腺神经内分泌肿瘤(PNET)的有用标志物。然而,尚未检查内镜超声引导细针抽吸细胞学中的INSM1表达。我们在被诊断为PNets的病例细胞学中评估了INSM1表达。方法对14个PNET病例中的免疫细胞化学染色INSM1和KI-67,并根据2017年世界卫生组织标准,七级1级病例,4级2例和三级3级/神经内分泌癌病例。作为INSM1和KI-67表达的对照,我们使用15例胰腺导管腺癌的细胞学标本。结果在PNET的全部细胞学标本中鉴定了PNET病例,在所有细胞学标本中鉴定了INSM1表达的肿瘤细胞。 1级病例中的中位数INSM1表达率为49.8%(平均值+/-标准差:55.1 +/- 12.5%,最小值:39.3%,最大值:74.1%),以及2年级和3级/神经内分泌癌病例81.1%(平均+/-标准差:77.6 +/- 18.6%,min:50.3%,最大:100%)。然而,INSM1和KI-67表达式(R = -0.15)之间没有相关性。 PNET病例中的中值表达率为64.3%,显着高于胰腺导管腺癌病例(P <0.0001)。结论内部镜下超声波引导细针吸入细胞学中的细胞学标本INSM1免疫细胞化学可以精确地诊断PNets;因此,INSM1可以是评估治疗策略的重要诊断工具,包括分子靶向治疗。

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