Ashby Elizabeth, Baker Markus, Eastwood Deborah M
Department of Orthopaedic Surgery, Great Ormond Street Hospital for Children, London, UK.
J Pediatr Orthop. 2016 Jun;36(4):370-5. doi: 10.1097/BPO.0000000000000463.
The purpose of this study is to describe the natural history of hip morphology in patients with mucopolysaccharidoses (MPS) I and MPS II.
This is a retrospective radiographic analysis of 88 hips in 44 children with MPS I and II. Radiographs were examined to determine hip migration, femoral head sphericity, and acetabular dysplasia at different ages throughout childhood. In individual hips, change in morphology and rate of change were analyzed.
There was a high rate of hip migration and femoral head dysplasia in both MPS I and MPS II. Progressive migration was seen in three quarters of hips and progressive femoral head deformity in over half of hips. Acetabular dysplasia was variable, ranging from normal to severely dysplastic, but did not change with time. Overall, hips were more dysplastic in MPS I than MPS II.
Hip morphology is variable in MPS I and MPS II ranging from almost normal to severely dysplastic. Some hips do not deteriorate with time and thus surgical intervention may not be necessary in all cases. Deterioration is slow allowing time to plan a holistic approach to treatment.
Level IV-case series.
本研究旨在描述黏多糖贮积症(MPS)I型和MPS II型患者髋关节形态的自然史。
这是一项对44例MPS I型和II型患儿的88个髋关节进行的回顾性影像学分析。对X线片进行检查,以确定整个儿童期不同年龄时髋关节的移位情况、股骨头的球形度以及髋臼发育不良情况。对各个髋关节的形态变化和变化率进行了分析。
MPS I型和MPS II型患者的髋关节移位率和股骨头发育不良率均较高。四分之三的髋关节出现进行性移位,超过一半的髋关节出现进行性股骨头畸形。髋臼发育不良情况各异,从正常到严重发育不良不等,但不随时间变化。总体而言,MPS I型患者的髋关节比MPS II型患者的更发育不良。
MPS I型和MPS II型患者的髋关节形态各异,从几乎正常到严重发育不良。一些髋关节不会随时间恶化,因此并非所有病例都需要手术干预。恶化过程缓慢,有时间规划整体治疗方法。
IV级——病例系列。