Bertoni F, Picci P, Bacchini P, Capanna R, Innao V, Bacci G, Campanacci M
Cancer. 1983 Aug 1;52(3):533-41. doi: 10.1002/1097-0142(19830801)52:3<533::aid-cncr2820520325>3.0.co;2-b.
Mesenchymal chondrosarcoma of bone and soft tissues treated at the Istituto Ortopedico Rizzoli are reviewed. The skeletal locations were prominent in five cases. Only two cases were in the soft tissues. Radiographic picture in the bone shows an aggressive osteolysis, with soft tissues invasion. Histologic picture is the same in bone and soft tissues, and is highly distinctive: islands of well-differentiated chondrosarcoma embedded in undifferentiated mesenchymal cells with high malignancy characteristics. The cases showed a poor prognosis, and no patient survived more than four years.
对在里佐利骨科研究所接受治疗的骨与软组织间叶性软骨肉瘤进行了回顾性研究。5例病变主要位于骨骼部位。仅有2例位于软组织。骨病变的影像学表现为侵袭性骨质溶解并伴有软组织侵犯。骨与软组织的组织学表现相同,且具有高度特异性:分化良好的软骨肉瘤岛状结构嵌入具有高恶性特征的未分化间叶细胞中。这些病例预后较差,无患者存活超过4年。