Delcambre B, Flipo R M, Leroux J L, Duquesnoy B
Service de Clinique Rhumatologique, Centre André Verhaeghe, Hôpital de la Charité, Lille, France.
Skeletal Radiol. 1989;18(1):21-4. doi: 10.1007/BF00366765.
Two inherited cases of osteomesopyknosis are reported. This is an autosomal dominant osteosclerosis described by Maroteaux in 1980; its radiological abnormalities consist of increased density of the vertebral plates, pelvis, and sometimes of the upper part of the femur. Osteomesopyknosis, usually discovered incidentally on radiographic examination, is a mild form of familial osteosclerosis and must be distinguished from osteopetrosis which carries a worse prognosis.
报告了两例遗传性骨致密症病例。这是一种1980年由马罗泰描述的常染色体显性遗传性骨硬化症;其放射学异常表现为椎板、骨盆以及有时股骨上部密度增加。骨致密症通常在X线检查时偶然发现,是一种轻度的家族性骨硬化症,必须与预后较差的骨石化症相鉴别。