Vanoli Alessandro, Argenti Francesca, Vinci Alessio, La Rosa Stefano, Viglio Alessandra, Riboni Roberta, Necchi Vittorio, Pugliese Luigi, Sessa Fausto, Pietrabissa Andrea, Paulli Marco
Department of Pathology, Fondazione IRCCS Policlinico San Matteo, and Department of Molecular Medicine, University of Pavia, Pavia, Italy,
Virchows Arch. 2015 Aug;467(2):237-45. doi: 10.1007/s00428-015-1788-6. Epub 2015 May 20.
We report a case of tumour in the head of the pancreas observed in a 57-year-old man with a history of worsening jaundice and elevated alpha-fetoprotein (AFP) serum level, who underwent Whipple pancreatoduodenectomy. Histologically, the tumour was predominantly composed of solid sheets of large eosinophilic cells with a prominent lymphoid infiltration without association neither with DNA microsatellite instability nor Epstein-Barr virus infection. The tumour was diffusely and strongly positive for hepatocyte paraffin-1 (Hep Par-1) and glypican-3 leading to the diagnosis of hepatoid carcinoma. Strong cytoplasmic staining for AFP was focally observed. Moreover, tumour cells showed countless cytoplasmic eosinophilic globules immunoreactive for the stress protein p62. A primary hepatocellular carcinoma of the liver was ruled out by careful clinical analysis. Hepatoid carcinoma is an extremely rare pancreatic neoplasm, and here, we describe the first case of such variant associated with lymphoid stroma. The characteristic histologic features and the immunophenotypic profile help in distinguishing this carcinoma from other pancreatic tumours, notably from medullary carcinoma.
我们报告一例发生于一名57岁男性胰头的肿瘤病例。该患者有黄疸加重及血清甲胎蛋白(AFP)水平升高的病史,接受了惠普尔胰十二指肠切除术。组织学上,肿瘤主要由大片大嗜酸性细胞构成,伴有显著的淋巴浸润,与DNA微卫星不稳定性及EB病毒感染均无关。肿瘤对肝细胞石蜡-1(Hep Par-1)和磷脂酰肌醇蛋白聚糖-3呈弥漫性强阳性,从而诊断为肝样癌。局部观察到AFP呈强细胞质染色。此外,肿瘤细胞显示出无数对应激蛋白p62呈免疫反应性的细胞质嗜酸性小球。通过仔细的临床分析排除了原发性肝癌。肝样癌是一种极其罕见的胰腺肿瘤,在此我们描述首例与淋巴间质相关的此类变异型病例。其特征性组织学特征和免疫表型有助于将这种癌与其他胰腺肿瘤区分开来,尤其是与髓样癌相鉴别。