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前列腺穿刺活检中单发小灶不典型时病理医师诊断意见的差异。

Variability in diagnostic opinion among pathologists for single small atypical foci in prostate biopsies.

机构信息

Department of Pathology, 11th floor, University Health Network, 200 Elizabeth Street, Toronto M5G 2C4, Canada.

出版信息

Am J Surg Pathol. 2010 Feb;34(2):169-77. doi: 10.1097/PAS.0b013e3181c7997b.

Abstract

Pathologists are increasingly exposed to prostate biopsies with small atypical foci, requiring differentiation between adenocarcinoma, atypical small acinar proliferation suspicious for malignancy, and a benign diagnosis. We studied the level of agreement for such atypical foci among experts in urologic pathology and all-round reference pathologists of the European Randomized Screening study of Prostate Cancer (ERSPC). For this purpose, we retrieved 20 prostate biopsies with small (most <1 mm) atypical foci. Hematoxylin and eosin-stained slides, including 10 immunostained slides were digitalized for virtual microscopy. The lesional area was not marked. Five experts and 7 ERSPC pathologists examined the cases. Multirater kappa statistics was applied to determine agreement and significant differences between experts and ERSPC pathologists. The kappa value of experts (0.39; confidence interval, 0.29-0.49) was significantly higher than that of ERSPC pathologists (0.21; confidence interval, 0.14-0.27). Full (100%) agreement was reached by the 5 experts for 7 of 20 biopsies. Experts and ERSPC pathologists rendered diagnoses ranging from benign to adenocarcinoma on the same biopsy in 5 and 9 biopsies, respectively. Most of these lesions comprised between 2 and 5 atypical glands. The experts diagnosed adenocarcinoma (49%) more often than the ERSPC pathologists (32%) (P<0.001). As agreement was particularly poor for foci comprising <6 glands, we would encourage pathologists to obtain intercollegial consultation of a specialized pathologist for these lesions before a carcinoma diagnosis, whereas clinicians may consider to perform staging biopsies before engaging on deferred or definite therapy.

摘要

病理学家越来越多地接触到具有小异型灶的前列腺活检,需要区分腺癌、疑似恶性的小腺泡异型增生和良性诊断。我们研究了泌尿科病理学家和欧洲前列腺癌随机筛查研究(ERSPC)的全能参考病理学家对这些异型灶的专家间一致性。为此,我们检索了 20 例具有小(大多数<1mm)异型灶的前列腺活检。苏木精和伊红染色切片,包括 10 张免疫染色切片,进行了数字化虚拟显微镜检查。未标记病变区域。5 名专家和 7 名 ERSPC 病理学家检查了病例。多评估者kappa 统计用于确定专家和 ERSPC 病理学家之间的一致性和显著差异。专家的kappa 值(0.39;置信区间,0.29-0.49)明显高于 ERSPC 病理学家的kappa 值(0.21;置信区间,0.14-0.27)。5 名专家中有 7 名对 20 个活检中的 7 个活检达到了完全(100%)一致。专家和 ERSPC 病理学家对同一次活检的诊断范围从良性到腺癌不等,分别为 5 个和 9 个活检。这些病变大多由 2 到 5 个异型腺组成。专家诊断腺癌(49%)的频率高于 ERSPC 病理学家(32%)(P<0.001)。由于包含<6 个腺体的病灶的一致性特别差,我们鼓励病理学家在诊断为癌前,为这些病变获得专门病理学家的同行咨询,而临床医生可能会考虑在进行推迟或明确治疗之前进行分期活检。

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