Suppr超能文献

成骨不全症。脊柱畸形的影像学分类、自然病史及治疗

Osteogenesis imperfecta. Radiographic classification, natural history, and treatment of spinal deformities.

作者信息

Hanscom D A, Winter R B, Lutter L, Lonstein J E, Bloom B A, Bradford D S

机构信息

Gillette Children's Hospital, St. Paul, Minnesota.

出版信息

J Bone Joint Surg Am. 1992 Apr;74(4):598-616.

PMID:1583055
Abstract

The natural history of the radiographic changes associated with osteogenesis imperfecta was recorded for sixty-four patients. Detailed clinical data regarding spinal deformities were available for forty-three patients. The patients could be placed in six well defined groups on the basis of a cluster of radiographic changes. The radiographic criteria used to classify patients who had osteogenesis imperfecta included the shape, dimensions, and appearance of the long bones; the presence of a trefoil pelvis and protrusio acetabuli; and the shape of the vertebrae. Patients can be classified more accurately if the dynamic nature of the radiographic changes is appreciated. Patients who had Type-A disease, a mild form of osteogenesis imperfecta, maintained the contours of the vertebrae. Most had straight long bones except for five patients who had mild bowing. Patients who had Type-B disease had bowed long bones with wide cortices. The pelvis had a normal contour. The vertebral bodies were biconcave, and kyphosis and scoliosis developed. Patients who had Type-C disease had thin, bowed long bones, and protrusio acetabuli developed around the age of ten years. Patients who had Type-D disease had the same findings as those who had Type-C disease, with the additional finding of cystic changes around the knee by the age of five years. The physes closed early, and the cysts disappeared around the age of fifteen. Patients who had Type-C or D disease had development of severe spinal deformities. Patients who had Type-E disease were totally dependent functionally, and spinal deformities developed at a very early age. The long bones appeared to have no cortex. Patients who had Type-F disease had complete disruption of the ribs, which was incompatible with survival. The natural history of scoliosis in the patients who had Type-B, C, D, or E disease was one of progression of the curve. Bracing used in the treatment of scoliosis in one patient who had Type-E disease and five patients who had Type-C disease was unsuccessful. Arthrodesis of the spine prevented progression of the spinal deformities in patients who had Type-A disease, but the results of the operation were variable in the remaining types of the disease.

摘要

记录了64例与成骨不全相关的影像学改变的自然病程。43例患者有关于脊柱畸形的详细临床资料。根据一系列影像学改变,患者可分为六个明确的组。用于对成骨不全患者进行分类的影像学标准包括长骨的形状、尺寸和外观;三叶骨盆和髋臼前突的存在;以及椎体的形状。如果认识到影像学改变的动态性质,患者可以得到更准确的分类。患有A型疾病(成骨不全的一种轻度形式)的患者,椎体轮廓保持不变。除5例有轻度弓形的患者外,大多数患者的长骨是直的。患有B型疾病的患者长骨呈弓形且皮质较宽。骨盆轮廓正常。椎体呈双凹形,出现后凸和侧凸。患有C型疾病的患者长骨细且呈弓形,约10岁时出现髋臼前突。患有D型疾病的患者与患有C型疾病的患者有相同的表现,另外在5岁时膝关节周围出现囊性改变。骨骺过早闭合,囊肿在15岁左右消失。患有C型或D型疾病的患者会出现严重的脊柱畸形。患有E型疾病的患者在功能上完全依赖他人,且在很小的年龄就出现脊柱畸形。长骨似乎没有皮质。患有F型疾病的患者肋骨完全断裂,这与存活不相容。患有B型、C型、D型或E型疾病的患者脊柱侧凸的自然病程是曲线进展。对1例患有E型疾病和5例患有C型疾病的患者使用支具治疗脊柱侧凸未成功。脊柱融合术可防止A型疾病患者的脊柱畸形进展,但在其余类型的疾病中手术结果不一。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验