Müller E, Majer R
Laryngol Rhinol Otol (Stuttg). 1975 Dec;54(12):933-41.
Bone like in otosclerosis from a 34-years-old man, from 33 years and 22 years old women, suffering from osteogenesis imperfecta tarda, with hardness of hearing in both ears were removed with chisel from the lower border of the oval window. After that a stapedectomy was accomplished. The stapedial crura have been genetically interrupted or broken, the footplate attached to the oval window. The bone from the border of the oval window was prepared for the histological examination. The specimens were coloured with Hematoxylin-Eosin and corresponding to Gomöri. In the bone similar cartilage osteoclasia and osteogenesis are rare. There are in the chondroosseous bone rooms filled with connective tissue. The diseased osseous labyrinth in osteo genesis imperfecta tarda must be regarded as a special morphogenetic formation of osteopsathyrosis.
取自一名34岁男性、一名33岁女性和一名22岁女性的耳硬化症骨质,这些女性患有迟发性成骨不全症且双耳听力减退,从椭圆窗下缘用凿子取出。之后进行了镫骨切除术。镫骨脚在遗传上中断或断裂,镫骨底板附着于椭圆窗。取自椭圆窗边的骨质准备用于组织学检查。标本用苏木精-伊红染色并对应Gomöri染色法。在骨质中,类似软骨破骨细胞活动和成骨现象罕见。在软骨骨腔中有结缔组织填充。迟发性成骨不全症中患病的骨迷路必须被视为骨质疏松症的一种特殊形态发生形成。