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泌尿道内翻性乳头状瘤的临床与分子学综述:如何应对?

A clinical and molecular review of inverted papilloma of the urinary tract: how to handle?

作者信息

Jørgensen Peter Hjorth, Vainer Ben, Hermann Gregers Gautier

机构信息

Department of Urology, Bispebjerg and Frederiksberg Hospitals, University of Copenhagen, Copenhagen, Denmark.

Department of Pathology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

出版信息

APMIS. 2015 Nov;123(11):920-9. doi: 10.1111/apm.12456. Epub 2015 Sep 11.

Abstract

Inverted papilloma (IP) of the urinary tract is classified by the World Health Organisation as a non-invasive urothelial tumour with normal to minimal cytological atypia of the neoplastic cells. During the 1980s, it came under suspicion of having a premalignant or malignant potential and of being concurrent with urothelial cell carcinoma (UCC). This quandary has been proven difficult to solve, due to the fact that IP is very rare and literature mostly consists of case reports with varying levels of information, making strong meta-analyses problematic. New immunohistochemical techniques and genetic approaches are more frequently being used in the attempt to achieve better classifications, prognosis and treatment of lesions hereunder IP. This review will, in our awareness, be the first to combine the knowledge from retrospective studies with these new approaches for determining a possible premalignant potential and concurrency with UCC and subsequently outline a recommendation for follow-up.

摘要

世界卫生组织将尿路内翻性乳头状瘤(IP)归类为一种非侵袭性尿路上皮肿瘤,其肿瘤细胞的细胞学异型性正常至极小。在20世纪80年代,它开始被怀疑具有恶变前或恶变潜能,并且与尿路上皮细胞癌(UCC)并存。由于IP非常罕见,而且文献大多是信息水平各异的病例报告,这使得进行有力的荟萃分析存在问题,因此这个难题一直难以解决。新的免疫组织化学技术和基因方法越来越多地被用于尝试对IP相关病变进行更好的分类、预后评估和治疗。据我们所知,本综述将首次把回顾性研究的知识与这些新方法相结合,以确定可能的恶变前潜能以及与UCC的并存情况,并随后概述随访建议。

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