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青年特发性骨质疏松症

Idiopathic osteoporosis in the young.

作者信息

Smith R

出版信息

J Bone Joint Surg Br. 1980 Nov;62-B(4):417-27. doi: 10.1302/0301-620X.62B4.7430216.

Abstract

Six patients are described with idiopathic osteoporosis which began between the ages of 4 and 16 years. In four children the disorder was mild with pain in the back, vertebral collapse, qualitatively normal iliac bone biopsies, variable calcium balance and spontaneous recovery. The two remaining patients had progressive bone disease with deformity. One with a previously normal skeleton developed changes similar to those of osteogenesis imperfecta; in the other patient, who rapidly developed structural collapse associated with severe metaphysial osteoporosis, treatment was ineffective and the histological appearances of the bone suggested osteoblastic failure. Quantitative bone histology in four patients showed no evidence of excessive active resorption; and the ratio of Type III to Type I collagen in the skin was normal, in contrast to the findings in osteogenesis imperfecta. The significance of this study in relation to previous accounts is reviewed.

摘要

本文描述了6例特发性骨质疏松症患者,发病年龄在4岁至16岁之间。4例儿童病情较轻,表现为背部疼痛、椎体塌陷、髂骨活检质量正常、钙平衡各异以及自发恢复。其余2例患者患有进行性骨病并伴有畸形。其中1例既往骨骼正常,出现了类似于成骨不全的变化;另1例患者迅速出现与严重干骺端骨质疏松相关的结构塌陷,治疗无效,骨组织学表现提示成骨细胞功能衰竭。4例患者的定量骨组织学检查未发现过度活跃吸收的证据;皮肤中III型与I型胶原蛋白的比例正常,这与成骨不全的表现不同。本文回顾了该研究相对于以往报道的意义。

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