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胆管狭窄中恶性肿瘤的形态学和分子诊断标准。

Morphologic and molecular diagnostic criteria of malignancies in biliary strictures.

作者信息

Albertini Elisa, Miranda Lucia, Maloberti Thais, de Biase Dario, Vasuri Francesco

机构信息

Pathology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.

School of Anatomic Pathology, Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.

出版信息

Histol Histopathol. 2025 Apr;40(4):443-452. doi: 10.14670/HH-18-811. Epub 2024 Sep 10.

Abstract

The differential diagnosis of benign and malignant biliary strictures is not always feasible and still represents a major diagnostic challenge, mainly due to the scarcity of the tissue retrieved for proper cytological or histopathological diagnosis. The present review focuses on morphological criteria in the diagnosis of biliary strictures, in the course of primary sclerosing cholangitis and other pathologies, starting from the limits of the cytological and histological evaluation, as well as the ancillary methodologies currently available in Pathology laboratories The current guidelines suggest fluorescence hybridization for the analysis of chromosomes 3, 7, and 17 polysomies and deletion of the 9p21 locus; however, other more promising techniques are on the horizon for both patient care and research purposes, such as Next-Generation Sequencing, able to analyze multiple genes simultaneously in a cost-effective fashion. Lastly, the most recent approaches proposed in the literature for the differential diagnosis of biliary stricture are described, such as circulating tumor DNA, miRNAs, and DNA methylation, among others.

摘要

良性和恶性胆管狭窄的鉴别诊断并非总是可行,仍然是一项重大的诊断挑战,主要是因为用于进行适当细胞学或组织病理学诊断的获取组织稀缺。本综述重点关注在原发性硬化性胆管炎及其他病理过程中胆管狭窄诊断的形态学标准,从细胞学和组织学评估的局限性,以及病理实验室目前可用的辅助方法开始。当前指南建议采用荧光杂交分析3号、7号和17号染色体多体性以及9p21位点缺失;然而,出于患者护理和研究目的,其他更有前景的技术即将出现,如下一代测序,它能够以经济高效的方式同时分析多个基因。最后,描述了文献中提出的用于胆管狭窄鉴别诊断的最新方法,如循环肿瘤DNA、微小RNA和DNA甲基化等。

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