Cribriform versus Intraductal: How to Determine the Difference

被引:0
|
作者
Comperat, Eva [1 ]
Klaeger, Johannes [1 ]
Rioux-Leclercq, Nathalie [2 ]
Oszwald, Andre [1 ]
Wasinger, Gabriel [1 ]
机构
[1] Med Univ Vienna, Dept Pathol, A-1090 Vienna, Austria
[2] CHU Rennes, Dept Pathol, F-35033 Rennes, France
关键词
prostate cancer; intraductal carcinoma; cribriform; pathological risk factors; PROSTATIC INTRAEPITHELIAL NEOPLASIA; GLEASON PATTERN 4; 2005; INTERNATIONAL-SOCIETY; ISUP CONSENSUS CONFERENCE; HISTOLOGIC FEATURES; PROGNOSTIC VALUE; CANCER PATIENTS; NEEDLE-BIOPSY; CARCINOMA; ADENOCARCINOMA;
D O I
10.3390/cancers16112002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Prostate cancer is a common and challenging disease among men, driving researchers to find better ways to understand and manage it. The understanding of two specific types, cribriform and intraductal prostate cancer (IDC-P), has evolved significantly over the years. This review aims to help pathologists differentiate between cribriform prostate cancer and IDC-P, and addresses current recommendations. Recent studies show that including these features in decision-making tools enhances predictions of cancer recurrence, spread, and patient outcomes. Future research should further focus on their pathological and molecular aspects to improve risk stratification, treatment approaches, and patient care.Abstract Over the years, our understanding of cribriform and intraductal prostate cancer (PCa) has evolved significantly, leading to substantial changes in their classification and clinical management. This review discusses the histopathological disparities between intraductal and cribriform PCa from a diagnostic perspective, aiming to aid pathologists in achieving accurate diagnoses. Furthermore, it discusses the ongoing debate surrounding the different recommendations between ISUP and GUPS, which pose challenges for practicing pathologists and complicates consensus among them. Recent studies have shown promising results in integrating these pathological features into clinical decision-making tools, improving predictions of PCa recurrence, cancer spread, and mortality. Future research efforts should focus on further unraveling the biological backgrounds of these entities and their implications for clinical management to ultimately improve PCa patient outcomes.
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页数:10
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