Fonseca S, Hoton D, Dardenne S, Annet L, Hubert C, Godecharles S, Jouret-Mourin A, Reding R, Otte J B, Rahier J, Gigot J F, Sempoux C
Service d'Anatomie Pathologique, Cliniques Universitaires Saint-Luc, UCL, Avenue Hippocrate, 10, 1200 Brussels, Belgium.
Int J Hepatol. 2013;2013:398308. doi: 10.1155/2013/398308. Epub 2013 Feb 28.
Light has been shed on the genotype/phenotype correlation in hepatocellular adenoma (HCA) recognizing HNF1 α -inactivated HCA (H-HCA), inflammatory HCA (IHCA), and β -catenin-activated HCA (b-HCA). We reviewed retrospectively our surgical HCA series to learn how to recognize the different subtypes histopathologically and how to interpret adequately their immunohistochemical staining. From January 1992 to January 2012, 37 patients underwent surgical resection for HCA in our institution. Nine had H-HCA (25%) characterized by steatosis and loss of L-FABP expression; 20 had IHCA (55.5%) showing CRP and/or SAA expression, sinusoidal dilatation, and variable inflammation; and 1 patient had both H-HCA and IHCA. In 5 patients (14%), b-HCA with GS and β -catenin nuclear positivity was diagnosed, two already with hepatocellular carcinoma. Two cases (5.5%) remained unclassified. One of the b-HCA showed also the H-HCA histological and immunohistochemical characteristics suggesting a subgroup of β -catenin-activated/HNF1 α -inactivated HCA, another b-HCA exhibited the IHCA histological and immunohistochemical characteristics suggesting a subgroup of β -catenin-activated/inflammatory HCA. Interestingly, three patients had underlying vascular abnormalities. Using the recently published criteria enabled us to classify histopathologically our retrospective HCA surgical series with accurate recognition of b-HCA for which we confirm the higher risk of malignant transformation. We also underlined the association between HCA and vascular abnormalities.
肝细胞腺瘤(HCA)中已揭示了基因型/表型的相关性,识别出HNF1α失活型HCA(H-HCA)、炎症型HCA(IHCA)和β-连环蛋白激活型HCA(b-HCA)。我们回顾性分析了我们的手术HCA系列病例,以了解如何在组织病理学上识别不同亚型,以及如何充分解读其免疫组化染色结果。1992年1月至2012年1月,我们机构有37例患者因HCA接受手术切除。9例为H-HCA(25%),其特征为脂肪变性和L-FABP表达缺失;20例为IHCA(55.5%),表现为CRP和/或SAA表达、窦性扩张和不同程度的炎症;1例同时具有H-HCA和IHCA特征。5例(14%)被诊断为具有GS和β-连环蛋白核阳性的b-HCA,其中2例已伴有肝细胞癌。2例(5.5%)仍未分类。1例b-HCA还表现出H-HCA的组织学和免疫组化特征,提示为β-连环蛋白激活/HNF1α失活型HCA亚组;另1例b-HCA表现出IHCA的组织学和免疫组化特征,提示为β-连环蛋白激活/炎症型HCA亚组。有趣的是,3例患者存在潜在的血管异常。使用最近公布的标准使我们能够对回顾性HCA手术系列病例进行组织病理学分类,准确识别出b-HCA,我们证实其恶性转化风险更高。我们还强调了HCA与血管异常之间的关联。