Ozaki T, Hamada M, Taguchi K, Nakatsuka Y, Sugihara S, Inoue H
Department of Orthopaedic Surgery, Okayama University Medical School, Japan.
Arch Orthop Trauma Surg. 1993;113(1):46-8. doi: 10.1007/BF00440594.
An 18-month-old girl with lesions in the cortex of the bilateral tibiae and ulnae and right fibula is reported. The lesion in the right tibia disappeared after curettage and xenogeneic bone grafting, and the other lesions disappeared spontaneously by the age of 12 years. All lesions involved the bone cortex. The right tibia lesion exhibited the histopathological features of "zonal architecture" and a osteoblast rim formation around the trabeculae. We consider that osteofibrous dysplasia can involve systemically any long bone.
报告了一名18个月大的女孩,其双侧胫骨、尺骨和右侧腓骨皮质有病变。右侧胫骨病变在刮除术和异种骨移植后消失,其他病变在12岁时自发消失。所有病变均累及骨皮质。右侧胫骨病变表现出“带状结构”的组织病理学特征以及小梁周围成骨细胞边缘形成。我们认为骨纤维发育不良可全身性累及任何长骨。