Suppr超能文献

肝门部胆总管梭形细胞型未分化癌:1例报告

Spindle cell-type undifferentiated carcinoma of the common bile duct of the hepatic hilus: report of a case.

作者信息

Nakanishi Yoshitsugu, Ito Tomoo, Kubota Kanako, Takeda Hiroko, Yonemori Atsuya, Kawakami Hiroshi, Zen Yoh, Kondo Satoshi

机构信息

Department of Surgical Oncology, Division of Cancer Medicine, Hokkaido University Graduate School of Medicine, Kita-15, Nishi-7, Kita-Ku, Sapporo 060-8638, Japan.

出版信息

Surg Today. 2007;37(8):708-12. doi: 10.1007/s00595-007-3463-2. Epub 2007 Jul 26.

Abstract

Spindle cell-type undifferentiated carcinoma arising from the extrahepatic bile duct is extremely rare. We herein report a case of this type of carcinoma in the common bile duct of the hepatic hilus. A 59-year-old man was admitted to our hospital complaining of jaundice. The laboratory data revealed an elevation of the serum carbohydrate antigen 19-9 level. Cholangiography revealed a complete obliteration of the left hepatic bile duct and stenosis of the bile duct from the superior to the right hepatic bile duct. Computed tomography showed the tumor to measure 15 x 12 mm in the hepatic hilus, with the obliteration of the right to main trunk of the portal vein and a swollen lymph node in the hepato-duodenum ligament. Arteriography revealed a kink of the right hepatic artery; therefore an encasement of the right hepatic artery was suspected. We preoperatively diagnosed hilus bile duct carcinoma and scheduled a right trisection hepatectomy. Intraoperative frozen sections taken from the tumor and tissues around the hepatic arteries showed spindle and inflammatory cells; therefore an inflammatory pseudotumor was diagnosed intraoperatively. As the right hepatic bile duct was occluded, a right lobe hepatectomy was performed. However, a permanent section revealed both spindle cells and poorly differentiated tubular adenocarcinoma cells positive for CAM5.2, AE1/AE3, and vimentin. On the basis of these findings, the tumor was finally diagnosed to be spindle cell-type undifferentiated carcinoma. Unfortunately, the patient died of pulmonary infarction 11 days after the operation.

摘要

肝外胆管来源的梭形细胞型未分化癌极为罕见。我们在此报告一例发生于肝门部胆总管的此类癌。一名59岁男性因黄疸症状入院。实验室检查数据显示血清糖类抗原19-9水平升高。胆管造影显示左肝管完全闭塞,肝门至上右肝管的胆管狭窄。计算机断层扫描显示肝门部肿瘤大小为15×12毫米,门静脉右主干闭塞,肝十二指肠韧带处有一个肿大的淋巴结。动脉造影显示右肝动脉有扭结;因此怀疑右肝动脉被包绕。我们术前诊断为肝门部胆管癌,并计划行右半肝切除术。术中取自肿瘤及肝动脉周围组织的冰冻切片显示为梭形细胞和炎性细胞;因此术中诊断为炎性假瘤。由于右肝管闭塞,遂行右肝叶切除术。然而,永久切片显示梭形细胞和低分化管状腺癌细胞对CAM5.2、AE1/AE3和波形蛋白呈阳性反应。基于这些发现,该肿瘤最终被诊断为梭形细胞型未分化癌。不幸的是,患者术后11天死于肺梗死。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验