A Rare Case of Cholangiocellular Liver Cancer with Hematogenous Metastases and Organ Changes in the Generalization of the Process

O. Vorobeva
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Abstract

Introduction. Cholangiocellular cancer is a malignant tumor from the epithelium of the bile ducts. Intravital diagnosis is often difficult to make due to the absence of any definitive signs of cancer and problems with detecting the first signs. Following the relevance of the problem, a case of cholangiocellular liver cancer with generalized metastases is presented.Materials and methods. The analysis of the received supporting medical documentation and the description of macroand micropreparations using histological (hematoxylin and eosin staining) and immunohistochemical methods were carried out.Results and discussion. Patient L.M., 60 years old, died at home, was referred by a general practitioner to the pathology department for autopsy examination. During the forensic autopsy, the macroscopic examination revealed dense liver substance, a «tree-like» mass of gray-yellow-brown color on the sections around the portal vein and intrahepatic bile ducts, with involvement of the right and left liver lobes and multiple gray nodules located throughout the liver parenchyma. The intrahepatic bile ducts malfunction due to expanding tumor tissue. Histological examination revealed a moderately differentiated tumor growth of cholangiocellular carcinoma, consisting of polymorphic cells separated by layers of fibrous tissue with areas of necrosis, foci of cholestasis. Immunohistochemical analysis of the tumor tissue of the lungs, liver: cytokeratins CAM 5.2 (+). All groups of lymph nodes of hepatoduodenal ligament, along vesicular and common bile ducts, hepatic artery and portal vein, surrounding left gastric and common hepatic artery, as well as lymph nodes of posterior pancreaticoduodenal group and distant lymph nodes are celiac; upper mesenteric and paraaortic zones appear unremarkable. Cerebral edema, pulmonary edema and necronephrosis were reported.Conclusion. The presented case is of particular interest to practitioners owing to the absence of the characteristic lymph node metastases and presence of hematogenous metastases and development of multiple organ failure.
一例罕见的癌症血管细胞性肝癌血行转移及全身器官改变
介绍癌症是一种来自胆管上皮的恶性肿瘤。由于缺乏任何明确的癌症体征以及检测最初体征的问题,通常很难进行生命内诊断。根据问题的相关性,提出了一例癌症的广泛转移。材料和方法。使用组织学(苏木精和伊红染色)和免疫组织化学方法对收到的支持性医疗文件进行分析,并对宏观和微观修复进行描述。结果和讨论。患者L.M.,60岁,死于家中,由一名全科医生转介至病理科进行尸检。在法医尸检过程中,宏观检查显示肝脏物质致密,门静脉和肝内胆管周围的切片上有一个灰黄棕色的“树状”肿块,左右肝叶受累,整个肝实质上有多个灰色结节。肝内胆管因肿瘤组织扩张而出现功能紊乱。组织学检查显示,胆管细胞癌是一种中等分化的肿瘤生长,由多层纤维组织分离的多态性细胞组成,有坏死区和胆汁淤积灶。肺、肝肿瘤组织的免疫组织化学分析:细胞角蛋白CAM 5.2(+)。肝十二指肠韧带的各组淋巴结,沿着膀胱和总胆管、肝动脉和门静脉,围绕左胃和肝总动脉,以及胰十二指肠后组和远处淋巴结均为腹腔;肠系膜上区和主动脉旁区似乎并不明显。报告了脑水肿、肺水肿和坏死性肾病。结论由于没有典型的淋巴结转移,存在血行转移和多器官衰竭,医生对本病例特别感兴趣。
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