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应用石蜡包埋组织 DNA 流式细胞术分析对壶腹发育不良进行诊断、风险分层和处理。

Diagnosis, risk stratification, and management of ampullary dysplasia by DNA flow cytometric analysis of paraffin-embedded tissue.

机构信息

Department of Pathology, University of California at San Francisco, San Francisco, CA, 94143, USA.

Department of Pathology, University of Washington, Seattle, WA, 98195, USA.

出版信息

Mod Pathol. 2019 Sep;32(9):1291-1302. doi: 10.1038/s41379-019-0272-2. Epub 2019 Apr 11.

Abstract

The limited accuracy of endoscopic biopsy in detecting high-grade dysplasia or adenocarcinoma within ampullary adenoma or dysplasia has been reported. The natural history of ampullary dysplasia is also unclear, and there are no established guidelines to determine which patients with ampullary dysplasia require resection versus surveillance endoscopy. DNA flow cytometry was performed on 47 ampullary biopsies with low-grade dysplasia, 18 high-grade dysplasia, and 23 negative for dysplasia, as well as 11 cases of ampullary adenocarcinoma. Abnormal DNA content (aneuploidy or elevated 4N fraction > 6%) was identified in 9 (82%) of adenocarcinoma, 13 (72%) of high-grade dysplasia, 7 (15%) of low-grade dysplasia, and none (0%) of non-dysplastic mucosa. One-, 2-, and 7-year detection rates of high-grade dysplasia or adenocarcinoma in low-grade dysplasia patients with abnormal DNA content were 57%, 86%, and 88%, respectively, whereas low-grade dysplasia patients in the setting of normal DNA content had 1-, 2-, and 7-year detection rates of 10%, 10%, and 10%, respectively. The univariate and multivariate hazard ratios (HRs) for subsequent detection of high-grade dysplasia or adenocarcinoma in low-grade dysplasia patients with DNA content abnormality were 16.8 (p = <0.01) and 9.8 (p = <0.01), respectively. Among the 13 high-grade dysplasia patients with DNA content abnormality, 5 patients (38%) were subsequently found to have adenocarcinoma within a mean follow-up time of 3 months, whereas only 1 (20%) of the remaining 5 patients in the setting of normal DNA content developed adenocarcinoma in a month (HR = 2.6, p = 0.39). The overall 1- and 2-year detection rates of adenocarcinoma in all high-grade dysplasia patients (regardless of flow cytometric results) were 34% (95% confidence interval = 16-63%) and 47% (95% confidence interval = 23-79%), respectively. In conclusion, the majority of low-grade dysplasia patients (86%) in the setting of abnormal DNA content developed high-grade dysplasia or adenocarcinoma within 2 years and thus may benefit from resection, whereas those with normal DNA content may be followed with surveillance endoscopy. The presence of DNA content abnormality can also confirm a morphologic suspicion of high-grade dysplasia, which should be managed with resection, as nearly 50% of the high-grade dysplasia patients were found to have adenocarcinoma within 2 years.

摘要

已经有报道称,在内镜活检检测壶腹腺瘤或异型增生中高级别异型增生或腺癌时,其准确性有限。壶腹异型增生的自然史也不清楚,也没有确定的指南来确定哪些壶腹异型增生患者需要切除或进行内镜监测。对 47 例低级别异型增生、18 例高级别异型增生和 23 例非异型增生的壶腹活检进行了 DNA 流式细胞术检测,以及 11 例壶腹腺癌。在 9 例(82%)腺癌、13 例(72%)高级别异型增生、7 例(15%)低级别异型增生和 0 例(0%)非异型增生黏膜中发现异常 DNA 含量(非整倍体或 4N 分数升高>6%)。在异常 DNA 含量的低级别异型增生患者中,高级别异型增生或腺癌的 1 年、2 年和 7 年检出率分别为 57%、86%和 88%,而在正常 DNA 含量的低级别异型增生患者中,1 年、2 年和 7 年的检出率分别为 10%、10%和 10%。低级别异型增生患者中,DNA 含量异常的患者随后检测到高级别异型增生或腺癌的单变量和多变量危险比(HR)分别为 16.8(p<0.01)和 9.8(p<0.01)。在 13 例 DNA 含量异常的高级别异型增生患者中,5 例(38%)在平均随访 3 个月内发现腺癌,而在正常 DNA 含量的其余 5 例患者中,仅 1 例(20%)在 1 个月内发现腺癌(HR=2.6,p=0.39)。所有高级别异型增生患者(无论流式细胞术结果如何)的 1 年和 2 年总腺癌检出率分别为 34%(95%置信区间 16-63%)和 47%(95%置信区间 23-79%)。总之,异常 DNA 含量设置中的大多数低级别异型增生患者(86%)在 2 年内发展为高级别异型增生或腺癌,因此可能受益于切除,而那些 DNA 含量正常的患者可以进行内镜监测。DNA 含量异常的存在也可以证实高级别异型增生的形态学怀疑,应通过切除来处理,因为近 50%的高级别异型增生患者在 2 年内发现腺癌。

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