Sonoda T, Toyoshima S, Enjoji M, Kanematsu T, Inokuchi K
Acta Pathol Jpn. 1984 Jul;34(4):919-24. doi: 10.1111/j.1440-1827.1984.tb07623.x.
We treated a 67-year-old man with primary carcinoma and sarcoma arising from the different areas of the cirrhotic liver. Histologically the carcinoma was of hepatocellular origin and the sarcoma consisted mainly of poorly differentiated mesenchymal cells partly with a chondrosarcomatous component. Among nine similar cases reported in the literature, only one was a rhabdomyosarcoma and the others were described simply as of spindle cell variety without evidence of mesenchymal differentiation. In the present case, the sarcoma consisted of mesenchymal cells with distinctive areas of unequivocal chondrosarcoma.
我们治疗了一名67岁男性,其患有起源于肝硬化肝脏不同部位的原发性癌和肉瘤。组织学检查显示,癌为肝细胞起源,肉瘤主要由分化不良的间充质细胞组成,部分具有软骨肉瘤成分。在文献报道的9例类似病例中,只有1例是横纹肌肉瘤,其他病例仅被描述为梭形细胞类型,无间充质分化证据。在本病例中,肉瘤由具有明确软骨肉瘤特征区域的间充质细胞组成。