Effects of the Paris System on the Unsatisfactory Category in a Cytohistologic Correlation Study of Patients With Urothelial Carcinoma.

Karina Munhoz de Paula Alves Coelho, Hercilio Fronza, Paula de Carvalho, Giordano Barzotto Tagliari, Lara Cristina Carvalho de Tavares, Jaqueline Stall, Hortência Gomes da Silveira, Paulo Henrique Condeixa de França
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Abstract

Context.—: The main objectives of the Paris System are to detect high-grade urothelial carcinoma, to standardize morphologic criteria and the cytopathologic report, to reduce the prevalence of the atypia category, and to improve the malignancy risk stratification.

Objective.—: To compare the results and sensitivity of cytologic classification before and after reclassification by the Paris System.

Design.—: Urinary cytology samples from patients with a histologic diagnosis of urothelial carcinoma were reclassified on the basis of the Paris System categories. The diagnoses before reclassification were divided into 5 categories (A, B, C, D, E) and compared with the Paris System (I, II, III, IV, V). Sensitivity was calculated considering cytohistologic agreement in relation to high-grade urothelial carcinoma.

Results.—: A total of 111 urinary cytology samples from patients were analyzed, corresponding to 40 histologic samples; of these, 12 (30%) were high grade and the remaining were low grade. Comparison of the correlated categories showed an increase from 3 (3 of 111; 2.7%) (A) to 31 (31 of 111; 27.9%) (I) in unsatisfactory cases and a decrease from 67 (67 of 111; 60,0%) to 30 (30 of 111; 27.0%) in negative cases, while the atypia category remained unchanged (15 cases [15 of 111; 13.5%]) (C and III). Suspicious cases increased from 5 (5 of 111; 4.5%) (D) to 14 (14 of 111; 12.6%) (IV) and cases of urothelial carcinoma were unchanged (21 cases [21 of 111; 18.9%]) (E and V). Sensitivity was 69% for the previous classification and 90% for the Paris System.

Conclusions.—: The Paris System improved the sensitivity of urinary cytology and the standardization of the unsatisfactory criteria, with an increase of cases in this category and a decrease of cases previously classified as negative among patients with a subsequent histologic diagnosis of urothelial carcinoma.

巴黎系统对尿路上皮癌患者细胞组织学相关性研究中不满意类别的影响
背景巴黎系统的主要目标是检测高级别尿路上皮癌,统一形态学标准和细胞病理学报告,降低不典型类别的发生率,改善恶性肿瘤风险分层:比较巴黎系统重新分类前后细胞学分类的结果和敏感性:根据巴黎系统分类对组织学诊断为尿路上皮癌的患者的尿液细胞学样本进行重新分类。将重新分类前的诊断结果分为 5 类(A、B、C、D、E),并与巴黎系统(I、II、III、IV、V)进行比较。考虑到细胞组织学与高级别尿路上皮癌的一致性,对敏感性进行了计算:共分析了 111 份患者尿液细胞学样本,与 40 份组织学样本相对应;其中 12 份(30%)为高级别,其余为低级别。相关类别的比较显示,不满意病例从 3 例(111 例中有 3 例;2.7%)(A)增加到 31 例(111 例中有 31 例;27.9%)(I),阴性病例从 67 例(111 例中有 67 例;60.0%)减少到 30 例(111 例中有 30 例;27.0%),而非典型病例类别保持不变(15 例[111 例中有 15 例;13.5%])(C 和 III)。可疑病例从 5 例(111 例中有 5 例;4.5%)(D)增加到 14 例(111 例中有 14 例;12.6%)(IV),尿路上皮癌病例保持不变(21 例 [111 例中有 21 例;18.9%])(E 和 V)。先前分类的灵敏度为 69%,而巴黎系统的灵敏度为 90%:结论:巴黎系统提高了尿液细胞学检查的灵敏度,并统一了不满意标准,在随后经组织学诊断为尿路上皮癌的患者中,该类别病例增加,之前被归类为阴性的病例减少。
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