Hepatocellular Carcinoma with β-Catenin Mutation: Imaging and Pathologic Characteristics

Hepatocellular Carcinoma with β-Catenin Mutation: Imaging and Pathologic Characteristics
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DOI:
10.1148/radiol.14141315
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发表时间:
2015-06-01
期刊:
影响因子:
19.7
通讯作者:
Gabata, Toshifumi
Gabata, Toshifumi
中科院分区:
医学1区
文献类型:
--
作者:
Kitao, Azusa;Matsui, Osamu;Gabata, Toshifumi

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目的:为了明确肝细胞癌(HCC)与β-catenin突变相关的影像学特征及其与病理结果的关系,材料和方法:获得伦理委员会批准和知情同意。本研究分析了138例手术切除的HCC。将β-catenin及其转录产物谷氨酰胺合成酶(GS)的免疫组化表达分级并分为3组:β-catenin阳性GS阳性组(HCC伴β-catenin突变)、β-catenin阴性GS阳性组(HCC中度)和β-catenin阴性GS阴性组(HCC无β-catenin突变)。评价动态计算机断层扫描(CT)和钆塞酸增强磁共振(MR)成像(T1加权、T2加权、弥散加权和肝胆期成像)的临床、病理和影像学表现。评价β-连环蛋白、GS和有机阴离子转运多肽1B 3(钆塞酸摄取转运蛋白)免疫组化表达之间的相关性。结果:在弥散加权成像中,β-连环蛋白突变的肝癌(n = 27)的中位对比噪声比低于中度肝癌(n = 23)和无β-连环蛋白突变的肝癌(n = 84)(分别为13.2、24.4和27.0; P = 0.02),表观扩散系数较高(分别为1.33、1.13和1.12; P < .0001),对比噪声比更高(分别为0.58、-28.7和-45.0; P < .0001)和肝胆期较高的增强比(分别为0.90、0.50和0.42; P < .0001)。在病理学检查中,β-连环蛋白突变的HCC表现出假腺体增生和胆汁生成,分化程度更高(分别为P = 0.04、0.001和0.005)。β-catenin、GS和有机阴离子转运多肽1B 3的表达呈显著正相关(P < .0001)。具有β-连环蛋白突变的HCC表现出更高的分化程度,具有频繁的假腺体模式和胆汁产生,特征性的影像学表现包括钆塞酸增强MR成像的高增强比和扩散时的高表观扩散系数,加权成像(C)RSNA,2015年
Purpose: To identify the imaging features of hepatocellular carcinoma (HCC) associated with beta-catenin mutation and their relationship to pathologic findings.Materials and Methods: Institutional ethics committee approval and informed consent were obtained. One hundred thirty-eight surgically resected HCCs were analyzed in this study. Immunohistochemical expression of beta-catenin and its transcriptional product, glutamine synthetase (GS), were graded and classified into three groups: the beta-catenin positive and GS positive group (HCC with beta-catenin mutation), the beta-catenin negative and GS positive group (intermediate HCC), and the beta-catenin negative and GS negative group (HCC without beta-catenin mutation). Clinical, pathologic, and imaging findings from dynamic computed tomography (CT) and gadoxetic acid-enhanced magnetic resonance (MR) imaging (T1-weighted, T2-weighted, diffusion-weighted, and hepatobiliary phase imaging) were evaluated. Correlations among immunohistochemical expression of beta-catenin, GS, and organic anion transporting polypeptide 1B3 (uptake transporter of gadoxetic acid) were evaluated. The x(2), Kruskal-Wallis, and Spearman correlation tests were used.Results: HCCs with beta-catenin mutation (n = 27) showed a lower median contrast-to-noise ratio at diffusion-weighted imaging than did intermediate HCCs (n = 23) and HCCs without beta-catenin mutation (n = 84) (13.2, 24.4, and 27.0, respectively; P = .02), higher apparent diffusion coefficient (1.33, 1.13, and 1.12, respectively; P < .0001), higher contrast-to-noise ratio (0.58, -28.7, and -45.0, respectively; P < .0001) and higher enhancement ratio during the hepatobiliary phase (0.90, 0.50, and 0.42, respectively; P < .0001). At pathologic examination, HCCs with beta-catenin mutation showed pseudoglandular proliferation and bile production with a higher grade of differentiation (P = .04, .001, and .005, respectively). There were significant positive correlations among expression of beta-catenin, GS, and organic anion transporting polypeptide 1B3 (P < .0001).Conclusion: HCCs with beta-catenin mutation showed a higher grade of differentiation with frequent pseudoglandular patterns and bile production, and characteristic imaging findings included a high enhancement ratio at gadoxetic acid-enhanced MR imaging and a high apparent diffusion coefficient at diffusion-weighted imaging. (C)RSNA, 2015