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重度成骨不全症年轻患者的复杂脊柱畸形:当前概念综述

Complex spine deformities in young patients with severe osteogenesis imperfecta: current concepts review.

作者信息

Castelein R M, Hasler C, Helenius I, Ovadia D, Yazici M

机构信息

Department of Orthopaedic Surgery, University Medical Center Utrecht, The Netherlands.

Orthopaedic Department, Children's Hospital, University of Basel, Switzerland.

出版信息

J Child Orthop. 2019 Feb 1;13(1):22-32. doi: 10.1302/1863-2548.13.180185.

Abstract

The severity of osteogenesis imperfecta (OI), the associated reduced quality and quantity of collagen type I, the degree of bone fragility, ligamentous laxity, vertebral fractures and multilevel vertebral deformities all impair the mechanical integrity of the whole spinal architecture and relate to the high prevalence of progressive kyphoscoliotic deformities during growth. Bisphosphonate therapy may at best slow down curve progression but does not seem to lower the prevalence of deformities or the incidence of surgery. Brace treatment is problematic due to pre-existing chest wall deformities, stiffness of the curve and the brittleness of the ribs which limit transfer of corrective forces from the brace shell to the spine. Progressive curves entail loss of balance, chest deformities, pain and compromise of pulmonary function and eventually require surgical stabilization, usually around puberty. Severe vertebral deformities including deformed, small pedicles, highly brittle bones and chest deformities, short deformed trunks and associated issues like C-spine and cranial base abnormalities (basilar impressions, cervical kyphosis) as well as deformed lower and upper extremities are posing multiple peri- and intraoperative challenges. Hence, an early multidisciplinary approach (anaesthetist, pulmonologist, paediatric orthopaedic spine surgeon) is mandatory. This paper was written under the guidance of the Spine Study Group of the European Paediatric Orthopaedic Society. It highlights the most pertinent information given in the current literature and various practical aspects on surgical care of spine deformities in young OI patients based on the personal experience of the contributing authors.

摘要

成骨不全症(OI)的严重程度、与之相关的I型胶原蛋白质量和数量的降低、骨脆性程度、韧带松弛、椎体骨折以及多节段椎体畸形,均会损害整个脊柱结构的机械完整性,并与生长过程中进行性脊柱侧后凸畸形的高患病率相关。双膦酸盐治疗充其量只能减缓侧弯进展,但似乎并不能降低畸形的患病率或手术发生率。由于存在胸壁畸形、侧弯僵硬以及肋骨脆性,支具治疗存在问题,这限制了矫正力从支具外壳传递至脊柱。进行性侧弯会导致平衡丧失、胸部畸形、疼痛以及肺功能受损,最终通常在青春期前后需要进行手术固定。严重的椎体畸形,包括变形的、小的椎弓根、高度脆性的骨骼和胸部畸形、短小变形的躯干以及相关问题,如颈椎和颅底异常(基底凹陷、颈椎后凸)以及上下肢畸形,带来了多个围手术期和术中挑战。因此,早期多学科方法(麻醉师、肺科医生、小儿骨科脊柱外科医生)是必不可少的。本文是在欧洲小儿骨科学会脊柱研究组的指导下撰写的。它基于撰稿作者的个人经验,突出了当前文献中给出的最相关信息以及年轻OI患者脊柱畸形手术护理的各种实际方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f9f/6376432/25ebf8b1c92b/jco-13-022-g0001.jpg

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