Seret P, Basle M F, Rebel A, Renier J C, Saint-Andre J P, Bertrans G, Audran M
J Cancer Res Clin Oncol. 1987;113(4):392-9. doi: 10.1007/BF00397726.
The authors report 12 cases (8 men and 4 women) of sarcomatous degeneration in Paget's bone disease, with an average age of 72.3 years. Sarcomatous degeneration occurred often in polyostotic Paget's disease, and osteitis deformans was seen in 4 cases. Femur and pelvis were the most affected bones. Pain was a constant feature, whereas tumefaction and fracture were less common. Osteolytic lesions were more frequent than condensed or mixed lesions and radiological signs of malignancy were usually found. Seven cases were histologically classified as osteogenic sarcoma and 3 cases as fibrosarcoma. Electron microscopy was performed on 2 osteogenic sarcomas and in 1 case revealed microcylindrical inclusions in Pagetic osteoclasts and in multinucleated giant tumor cells, but none in mononucleated tumor cells. The average survival time for the patients in this study was only 4.5 months.
作者报告了12例佩吉特骨病肉瘤变病例(8例男性,4例女性),平均年龄72.3岁。肉瘤变常发生于多骨型佩吉特病,4例可见畸形性骨炎。股骨和骨盆是最常受累的骨骼。疼痛是持续存在的症状,而肿胀和骨折则较少见。溶骨性病变比致密性或混合性病变更常见,通常可发现恶性的放射学征象。7例组织学分类为骨肉瘤,3例为纤维肉瘤。对2例骨肉瘤进行了电子显微镜检查,1例显示佩吉特破骨细胞和多核巨肿瘤细胞中有微圆柱形包涵体,而单核肿瘤细胞中无此现象。本研究中患者的平均生存时间仅为4.5个月。