Ornoy A, Kim O J
Isr J Med Sci. 1977 Jan;13(1):26-32.
A case of osteogenesis imperfecta fetalis in a stillborn black male infant is described. Scanning electron microscopic studies of the skeleton showed normal intercartilaginous septa in the metaphyses of long bones, covered by uniform, calcifying globules 1 mum in diameter. In the diaphyses, however, the orientation of bone trabeculae was abnormal. The trabeculae were thin, with wide and densely packed osteocytic lacunae, and with more resorbing surfaces than in the control specimens. It is concluded that in osteogenesis imperfecta there is abnormal periosteal ossification, together with increased osteocytic resorption.
本文描述了一例死产黑人男婴的胎儿型成骨不全症。对其骨骼进行扫描电子显微镜研究显示,长骨干骺端的软骨内间隔正常,表面覆盖着直径为1微米的均匀钙化小球。然而,在骨干中,骨小梁的方向异常。骨小梁很细,骨细胞陷窝宽且密集,吸收表面比对照标本更多。得出的结论是,在成骨不全症中存在异常的骨膜骨化,同时骨细胞吸收增加。