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Cholangiolocellular carcinoma with rapid progression initially showing abnormally elevated serum alfa-fetoprotein

机译:进展迅速的胆管细胞癌最初显示血清阿尔法胎蛋白异常升高

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Cholangiolocellular carcinoma (CoCC) is a rare malignant liver tumor derived from hepatic progenitor cells, which exist in the canals of Hering. We encountered a case of CoCC with an extremely poor clinical course, initially showing abnormally elevated serum alfa-fetoprotein (AFP). A 72-year-old male presented with a liver tumor and abnormally elevated serum AFP levels (16,399 ng/ml). We preoperatively diagnosed hepatocellular carcinoma and performed extended right hepatectomy, after which the serum AFP levels remarkably decreased to 97 ng/ml. Postoperatively, the disease was pathologically diagnosed as CoCC. Furthermore, immunohistochemical pathological findings were alcian blue negative, cytokeratin (CK) 7 partially positive, CK19 positive, hepatocyte paraffin-1 negative, membranous negative for epithelial membrane antigen, and AFP negative. Fifty-five days later, intra- and extrahepatic recurrence developed, and the patient died 65 days after surgery. Although CoCCs show favorable outcomes, these characteristics of our case were not previously reported. It is necessary to accumulate more information on CoCC.
机译:胆管细胞癌(CoCC)是一种罕见的源自肝祖细胞的恶性肝肿瘤,其存在于黑灵运河中。我们遇到一例CoCC,其临床病程极其差,最初显示出血清甲胎蛋白(AFP)异常升高。一名72岁的男性出现肝脏肿瘤,血清AFP水平异常升高(16,399 ng / ml)。我们在术前诊断出肝细胞癌并进行了右肝扩大切除术,之后血清AFP水平显着降低至97 ng / ml。术后,该病在病理上被诊断为CoCC。此外,免疫组织化学病理学结果为阿尔辛蓝阴性,细胞角蛋白(CK)7部分阳性,CK19阳性,肝细胞石蜡1阴性,上皮膜抗原的膜性阴性和AFP阴性。五十五天后,出现肝内和肝外复发,患者在手术后65天死亡。尽管CoCC显示出有利的结局,但我们病例的这些特征以前未曾报道过。有必要积累有关CoCC的更多信息。

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