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Early hepatocellular carcinoma with high-grade atypia in small vaguely nodular lesions

机译:早期肝细胞癌伴不典型小结节性病变的高度异型性

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摘要

Multistep hepatocarcinogenesis progresses from dysplastic nodules to early hepatocellular carcinoma (eHCC) and to advanced HCC. The aim of the present study was to investigate the detailed histopathological features of eHCC. We investigated 66 small vaguely nodular lesions resected from 40 patients. The degree of cellular and structural atypia and stromal invasion were assessed. The immunohistochemical expression of HCC-related markers adenylate cyclase-associated protein 2 (CAP2), heat shock protein 70 (HSP70), Bmi-1, CD34 and h-caldesmon were evaluated. Of the 66 nodules, 10 were diagnosed as low-grade dysplastic nodules (LGDN), 10 as high-grade dysplastic nodules (HGDN) and 46 as eHCC. Among the 46 eHCC, 18 nodules (39.1%) showed marked stromal invasion and /or the presence of the scirrhous component and were subclassified as highgrade eHCC (HGeHCC). The remaining 28 eHCC, which lacked these features, were subclassified as low-grade eHCC (LGeHCC) and were examined further. HGeHCC showed high levels of cellular and structural atypia and large tumor size. The immunohistochemical expression of CAP2 and the area of sinusoidal vascularization showed increases from LGDN to HGeHCC. The density of arterial tumor vessels was high in HGeHCC compared with other nodule types. Cluster analysis of these parameters subclassified 65 nodules into HGeHCC-dominant, LGeHCC and HGDN-dominant, and LGDN-dominant groups. These results indicate the increased malignant potential of HGeHCC and suggest that it is already a transitional stage to advanced HCC. We consider that our grading classification system may be valuable for considering treatment strategies for eHCC around 2 cm in diameter.
机译:多步肝癌发生发展从增生性结节发展到早期肝细胞癌(eHCC)和晚期HCC。本研究的目的是调查eHCC的详细组织病理学特征。我们调查了从40例患者中切除的66个模糊的小结节性病变。评估细胞和结构异型性和间质侵犯的程度。评估了HCC相关标记腺苷酸环化酶相关蛋白2(CAP2),热休克蛋白70(HSP70),Bmi-1,CD34和h-caldesmon的免疫组织化学表达。在66个结节中,有10个被诊断为低度异常增生性结节(LGDN),有10个被诊断为高等级不典型增生结节(HGDN),有46个被诊断为eHCC。在46例eHCC中,有18个结节(39.1%)表现出明显的间质浸润和/或存在肝硬化成分,并被归类为高级eHCC(HGeHCC)。其余28个缺少这些功能的eHCC被归类为低级eHCC(LGeHCC),并进行了进一步检查。 HGeHCC显示出高水平的细胞和结构异型性和较大的肿瘤大小。从LGDN到HGeHCC,CAP2的免疫组织化学表达和正弦血管化面积均增加。与其他结节类型相比,HGeHCC的动脉肿瘤血管密度高。这些参数的聚类分析将65个结节分为HGeHCC为主,LGeHCC和HGDN为主,LGDN为主。这些结果表明,HGeHCC的恶性潜能增加,表明它已经是向晚期HCC过渡的阶段。我们认为我们的分级分类系统对于考虑直径约2 cm的eHCC的治疗策略可能是有价值的。

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