术前诊断困难的胆管细胞癌2例

Q4 Medicine
Yoshiteru Katsura, Koji Hayashi, Narumi Sawamura, Risa Kawamoto, Yo Akazawa, Ryuta Ueda, Masahiro Koh, Akio Hara, Hiroshi Takeyama, Natsumi Tanaka, Naomi Urano, Shu Okamura, Setsuko Yoshioka, Hideoki Yokouchi, Chikara Ebisui
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引用次数: 0

摘要

胆管细胞癌(CoCC)是一种罕见的原发性肝癌。我们报告2例胆管细胞癌(CoCC)。病例1:66岁男性。最初诊断为疑似肝血管瘤并随访,5个月后MRI增强呈增高趋势,诊断为肝内胆管癌,行手术治疗。病例2:73岁女性。她怀疑有肝血管瘤。8个月后,MRI造影显示增大20mm,怀疑肝细胞癌或肝内胆管癌,行手术治疗。两例患者病理诊断均为CoCC。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Two Cases of Cholangiolocellular Carcinoma with Difficult Preoperative Diagnosis].

Cholangiocellular carcinoma(CoCC)is a rare form of primary liver cancer. We report 2 cases of cholangiocellular carcinoma(CoCC). Case 1: 66-year-old male. He was initially diagnosed as a suspected hepatic hemangioma and followed up, but 5 months later, contrast-enhanced MRI showed an increasing trend, and he was diagnosed as intrahepatic cholangiocarcinoma and underwent surgery. Case 2: 73-year-old female. She was suspected to have hepatic hemangioma. Eight months later, contrast-enhanced MRI showed an enlargement of 20 mm in size, which led to suspicion of hepatocellular carcinoma or intrahepatic cholangiocarcinoma, and surgery was performed. The pathological diagnosis of both patients was CoCC.

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