Yoshida Naoki, Midorikawa Yutaka, Kajiwara Takahiro, Yoshida Nao, Nakayama Hisashi, Sugitani Masahiko, Takayama Tadatoshi
Department of Digestive Surgery, Nihon University School of Medicine, Tokyo, Japan.
Case Rep Gastroenterol. 2013 Mar 22;7(1):169-74. doi: 10.1159/000350558. Print 2013 Jan.
Hepatocellular carcinoma (HCC) with sarcomatoid change is a rare neoplasm of the liver, and recurrent therapies for HCC such as transcatheter arterial chemoembolization and percutaneous ablation therapy are presumed to promote sarcomatoid change. A 73-year-old man was admitted to our hospital diagnosed as having liver cancer originating from hepatitis C-related cirrhosis without any previous treatment for HCC. Ultrasonography showed that the tumor was hypoechoic, 3 cm in diameter, with unclear margins. Computed tomography demonstrated a low-density lesion with ring enhancement on delayed phase. Under a diagnosis of poorly differentiated HCC the patient underwent liver resection. Histologically, the tumor consisted of proliferation of spindle-shaped sarcomatoid carcinoma cells with unclear trabecular and pseudoglandular structures including a nodule of typical moderately differentiated HCC, which was observed to shift mutually in one region. Here, we report a case of sarcomatoid HCC with a review of the literature.
伴有肉瘤样变的肝细胞癌(HCC)是一种罕见的肝脏肿瘤,据推测,诸如经动脉化疗栓塞术和经皮消融治疗等HCC的复发性治疗会促进肉瘤样变。一名73岁男性因诊断为源自丙型肝炎相关肝硬化的肝癌而入住我院,此前未接受过任何HCC治疗。超声检查显示肿瘤为低回声,直径3cm,边界不清。计算机断层扫描显示延迟期有环形强化的低密度病变。在诊断为低分化HCC后,患者接受了肝切除术。组织学上,肿瘤由梭形肉瘤样癌细胞增殖组成,小梁和假腺结构不清晰,其中包括一个典型的中度分化HCC结节,在一个区域内相互移位。在此,我们报告一例肉瘤样HCC病例并复习文献。