Richter D, Bosse A, Weber A, Müller K M, Muhr G
Chirurgische Universitätsklinik und Poliklinik, Berufsgenossenschaftliche Kliniken Bergmannsheil, Bochum.
Langenbecks Arch Chir. 1995;380(6):354-8. doi: 10.1007/BF00207225.
The case of a 23-year-old female patient suffering from a rare variety of osteosarcoma of the distal femur with epithelial differentiation and only traces of osteoid is reported. The tumour cells reacted strongly to antibodies against vimentin. Metastases were found in the fifth rib and the right kidney. There was no response to chemotherapy. One year after implantation of a tumour prosthesis of the knee a thigh amputation was necessary because of a local failure. The patient died 2.5 years after the tumour had initially been diagnosed. Other reports of this rare type of epitheloid osteosarcoma illustrate the difficulties involved in reaching a correct diagnosis. This tumour can be mistaken for a skeletal metastasis of an epithelial tumour.
报告了一例23岁女性患者,患有罕见的股骨远端骨肉瘤,伴有上皮分化且仅有微量骨样组织。肿瘤细胞对波形蛋白抗体反应强烈。在第五肋骨和右肾发现转移灶。化疗无反应。在植入膝关节肿瘤假体一年后,因局部失败而不得不进行大腿截肢。患者在最初诊断出肿瘤2.5年后死亡。关于这种罕见类型上皮样骨肉瘤的其他报告说明了做出正确诊断所涉及的困难。这种肿瘤可能被误诊为上皮性肿瘤的骨转移。