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黏多糖贮积症的矫形挑战。

Orthopaedic challenges for mucopolysaccharidoses.

机构信息

Orthopaedic Clinic, Padua University General Hospital, Padua, Italy.

Department of Traumatology and Orthopaedic Surgery, San Gerardo Hospital Milano Bicocca Medical School, Monza, Italy.

出版信息

Ital J Pediatr. 2018 Nov 16;44(Suppl 2):123. doi: 10.1186/s13052-018-0557-y.

Abstract

Mucopolysaccharidoses (MPS) are a group of diseases characterized by abnormal accumulation of glycosaminoglycans (GAGs). Although there are differences among the various disease types, the osteoarticular system is always involved. The aim of the present study was to establish a framework for MPS-related orthopaedic manifestations and for their treatment. The authors, affiliated to three different Italian Orthopaedic Centres, report data taken from the literature reviewed in light of their accumulated professional experience. Bone alterations make up what is known as dysostosis multiplex, involving the trunk and limbs and with typical radiological findings. Joints are affected by pathological tissue infiltrations. The cervical spinal cord is involved, with stenosis and cervical and occipitocervical instability. In MPS there is a much higher incidence of scoliosis compared with healthy subjects without any particular distinctive feature. Kyphosis of the spine is more frequent and also more severe because of its possible neurological complications, and it is localized at the thoracolumbar level with a malformed vertebra at the top of the deformity. Evolving forms, and those associated with neurological damage, require anteroposterior spine fusion. The hip is invariably involved, with dysplasia affecting the femoral neck (coxa valga), the femoral epiphysis (loss of sphericity, osteonecrosis), and the femoral acetabulum which is flared. All these features explain the tendency to progressive hip migration. Genu valgum is often found (a deviation of the physiological axis with an obtuse angle opening laterally). This deformity is often localized at the proximal tibial metaphysis; it causes functional limitations and leads to an irregular erosion of the articular cartilage. In young patients who still have the growth plate, it is possible to execute a medial hemiepiphysiodesis, a temporary inhibition of cartilage growth, with progressive axis correction. In this paper, the characterisation of clinical features and the review of treatments are divided into separate sections based on the part of the body involved. The conclusions of each section are presented as a summary. One section discusses the high risk of anaesthesia-related complications requiring the collaboration of specifically trained personnel.

摘要

黏多糖贮积症(MPS)是一组以糖胺聚糖(GAG)异常积累为特征的疾病。尽管各种疾病类型存在差异,但骨骼关节系统总是受到影响。本研究旨在建立 MPS 相关骨科表现及其治疗的框架。作者隶属于三个不同的意大利骨科中心,根据他们积累的专业经验,报告了从文献综述中提取的数据。骨骼改变构成了所谓的多发性骨发育不良,涉及躯干和四肢,并具有典型的影像学发现。关节受到病理性组织浸润的影响。颈椎受累,伴有狭窄和颈椎及枕颈不稳。与没有任何特定特征的健康受试者相比,MPS 中脊柱侧凸的发生率要高得多。脊柱后凸更常见且更严重,因为其可能存在神经并发症,并且位于胸腰椎水平,畸形的顶部有一个畸形的椎体。进行性和与神经损伤相关的形式需要前后脊柱融合。髋关节总是受累,影响股骨颈(髋外翻)、股骨骨骺(球形丧失、骨坏死)和股骨髋臼,这些部位呈喇叭状张开。所有这些特征都解释了髋关节进行性迁移的趋势。常发现膝内翻(生理轴的偏离,形成钝角,向外侧张开)。这种畸形常位于胫骨近端干骺端;它导致功能受限,并导致关节软骨的不规则侵蚀。对于仍有生长板的年轻患者,可以进行内侧半骺阻滞术,暂时抑制软骨生长,从而逐渐纠正轴线。在本文中,根据所涉及的身体部位,将临床特征的描述和治疗方法的回顾分为单独的部分。每一部分的结论都作为一个总结呈现。有一节讨论了与麻醉相关的并发症风险较高,需要专门训练的人员的协作。

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