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使用内镜超声引导下细针穿刺抽吸/活检标本对胆管癌进行有前景的基因组检测。

Promising Genomic Testing for Biliary Tract Cancer Using Endoscopic Ultrasound-Guided Fine-Needle Aspiration/Biopsy Specimens.

作者信息

Kuwatani Masaki, Kawakubo Kazumichi, Sakamoto Naoya

机构信息

Department of Gastroenterology and Hepatology, Hokkaido University Hospital, North 14, West 5, Kita-ku, Sapporo 060-8648, Japan.

出版信息

Diagnostics (Basel). 2022 Apr 5;12(4):900. doi: 10.3390/diagnostics12040900.

Abstract

The undesired prognosis of biliary tract cancer is mainly attributed to the difficult detection of cancer lesions, including intraepithelial neoplasia and no standard examination for screening. In addition, pathological diagnosis of biliary stricture, whether it is malignant or benign, is not so easy, because of difficult optimal sampling by forceps biopsy and brush cytology, although various devices and methods for pathological diagnosis have been reported. Furthermore, we have to be careful about post-endoscopic retrograde cholangiography pancreatitis when we approach the biliary tract lesion via a transpapillary route. In order to improve the diagnostic accuracy, there have been several studies that indicate the feasibility and efficacy of genomic analysis for accurate diagnosis of biliary tract cancer by using pathological specimens, including endoscopic ultrasound-guided fine-needle aspiration/biopsy (EUS-FNA/FNB) samples. For efficient and precision medicine for patients with biliary tract cancer, future diagnosis and treatment should also be based on molecular and genetic analyses. In this article, we review and summarize the past knowledge and cutting edge of genomic testing for biliary tract cancer, using EUS-FNA/FNB specimens, and indicate some ingenuities in sample processing to promote effective clinical practice and future perspectives.

摘要

胆道癌不良的预后主要归因于癌症病变难以检测,包括上皮内瘤变,且缺乏标准的筛查检查。此外,由于钳取活检和刷检细胞学难以获取最佳样本,尽管已报道了各种用于病理诊断的设备和方法,但对胆道狭窄进行良恶性的病理诊断并非易事。此外,当我们经乳头途径接近胆道病变时,必须注意内镜逆行胰胆管造影术后胰腺炎。为了提高诊断准确性,已有多项研究表明,利用包括内镜超声引导下细针穿刺抽吸/活检(EUS-FNA/FNB)样本在内的病理标本进行基因组分析,对准确诊断胆道癌具有可行性和有效性。为了为胆道癌患者提供高效和精准的医疗,未来的诊断和治疗也应基于分子和基因分析。在本文中,我们回顾并总结了过去使用EUS-FNA/FNB标本对胆道癌进行基因组检测的知识和前沿进展,并指出样本处理中的一些技巧,以促进有效的临床实践和未来展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0cc/9030881/ea062ad20f01/diagnostics-12-00900-g001.jpg

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