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一名原发性硬化性胆管炎患者的肝内胆管梭形细胞癌。

Spindle cell carcinoma of the intrahepatic bile duct in a patient with primary sclerosing cholangitis.

作者信息

Shinoda Masahiro, Shimazu Motohide, Mukai Makio, Tanabe Minoru, Hashiguchi Naoko, Oda Masaya, Kitajima Masaki

机构信息

Department of Surgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.

出版信息

J Gastroenterol. 2003;38(11):1091-6. doi: 10.1007/s00535-003-1202-z.

Abstract

We present a case of spindle cell carcinoma of the intrahepatic bile duct that developed in a 34-year-old man with primary sclerosing cholangitis. At the time of presentation, the patient had a 10-year history of primary sclerosing cholangitis. A mass was found in the hepatic hilus and was resected surgically. The tumor was composed predominantly of spindle cells, and a small portion of the tumor appeared to be adenocarcinomatous by histology. Histological and immunohistochemical findings suggested that the spindle cells were epithelial in origin; thus, this tumor was identified as a spindle cell carcinoma. Spindle cell carcinomas arising in the bile duct are extremely rare. Furthermore, the coexistence of spindle cell carcinoma and primary sclerosing cholangitis has not been reported thus far. We were able to follow up the entire course of this rare case. In this case report, we describe the clinicopathological findings of this case and review the literature concerning this type of tumor.

摘要

我们报告一例肝内胆管梭形细胞癌,该病例发生于一名患有原发性硬化性胆管炎的34岁男性。在就诊时,患者有10年原发性硬化性胆管炎病史。在肝门处发现一个肿块,并进行了手术切除。肿瘤主要由梭形细胞组成,组织学检查显示肿瘤的一小部分似乎为腺癌。组织学和免疫组化结果表明梭形细胞起源于上皮;因此,该肿瘤被确定为梭形细胞癌。胆管发生的梭形细胞癌极为罕见。此外,迄今为止尚未报道过梭形细胞癌与原发性硬化性胆管炎并存的情况。我们得以对这一罕见病例的全过程进行随访。在本病例报告中,我们描述了该病例的临床病理特征,并回顾了有关此类肿瘤的文献。

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