应用 PI-RADS 2.1 的要点和陷阱

Ankur Pandey, Soumyadeep Ghosh, Priyanka Prajapati, Nabih Nakrour, M. Harisinghani
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引用次数: 0

摘要

前列腺成像报告和数据系统(PI-RADS)与多参数磁共振成像(MRI)的结合使用大大提高了对有临床意义的前列腺癌(csPCa)的检测率,但读者可能会面临一些挑战。本综述概述了与多参数前列腺磁共振成像(mpMRI)的 PI-RADS 系统相关的误区,并提出了有助于克服这些误区的建议/观点。此外,PI-RADS 系统的阳性预测值(PPV)在不同中心之间存在很大差异,凸显了改进的必要性。虽然 csPCa 的阴性预测值 (NPV) 一般较高,但也存在差异。本综述讨论了导致 FNs 的陷阱,包括 MRI 伪影,如易感和运动伪影。文中提出了优化图像采集的技术,如转换相位编码方向和减少肠蠕动,以减轻这些伪影。弥散加权成像(DWI)的b值选择不当是另一个陷阱,强调了使用高b值(≥1,400 s/mm2)优化肿瘤检测的重要性。同样,本文还讨论了优化窗口设置以观察 csPCa、正确定位肛门直肠内线圈、认识粘液腺癌和楔形腺癌等罕见变异以及区分中心区肿瘤和正常中心区等问题。本文重点介绍了导致 FP 的常见误区,如前列腺炎、肉芽肿性前列腺炎、前列腺脓肿、间质良性前列腺增生结节、挤压性良性前列腺增生结节和前列腺钙化等良性病变。它还讨论了与正常解剖结构有关的误区,包括中央区、前纤维肌基质、增厚的手术囊、神经血管束和前列腺周围静脉丛。文章介绍了仔细评估这些实体的形态和信号异常分布的技术,以避免将其过度诊断为 PCa。文章还讨论了与介入后变化有关的陷阱,包括活组织检查后出血和 UroLift 手术造成的伪影,同时提供了应对这些挑战的建议。最后,文章强调了分期过程中可能遇到的陷阱,包括评估前列腺外延伸、盆腔结节和骨转移。
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Pearls and Pitfalls in Applying PI-RADS 2.1
The use of Prostate Imaging Reporting and Data System (PI-RADS) with multiparametric magnetic resonance imaging (MRI) has significantly improved the detection of clinically significant prostate cancer (csPCa), but there are certain challenges that the reader may face. This review provides an overview of the pitfalls associated with the PI-RADS system for multiparametric prostate MRI (mpMRI), with suggestions/pearls to help overcome these pitfalls.PI-RADS assessment is hindered by several causes of false positives (FPs) and false negatives (FNs). In addition, there is wide variability in the positive predictive value (PPV) of the PI-RADS system across different centers, highlighting the need for improvement. While the negative predictive value (NPV) for csPCa is generally high, variations exist.This review discusses the pitfalls contributing to FNs, including MRI artifacts, such as susceptibility and motion artifacts. Techniques to optimize image acquisition, such as switching the phase encoding direction and reducing bowel peristalsis, are suggested to mitigate these artifacts. Improper b-value selection for diffusion-weighted imaging (DWI) is another pitfall, emphasizing the importance of using high b-values (≥1,400 s/mm2) to optimize neoplasm detection. Similarly, optimizing window settings to visualize csPCa, correctly positioning the endorectal coil, awareness of rare variants like mucinous adenocarcinoma and cribriform adenocarcinoma, and distinguishing central zone tumors from normal central zone are discussed.This article highlights the common pitfalls causing FPs, such as benign pathologies like prostatitis, granulomatous prostatitis, prostatic abscess, stromal BPH nodules, extruded BPH nodules, and prostatic calcifications. It also discusses the pitfalls related to normal anatomical structures, including the central zone, anterior fibromuscular stroma, thickened surgical capsule, neurovascular bundle, and periprostatic venous plexus. Techniques for carefully evaluating these entities' morphology and distribution of signal abnormalities are described to avoid overdiagnosing these as PCa. The article also addresses the pitfalls related to postintervention changes, including postbiopsy hemorrhage and artifacts caused by the UroLift procedure, while providing recommendations for managing these challenges.Finally, the pitfalls that may be encountered during staging, including evaluation for extraprostatic extension, and pelvic nodal and osseous metastases, are highlighted.
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