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致密性成骨不全症的骨科治疗:一项系统评价

Orthopedic Treatment of Pycnodysostosis: A Systematic Review.

作者信息

Taka Taha M, Lung Brandon, Stepanyan Hayk, So David, Yang Steven

机构信息

Orthopaedic Surgery, University of California Riverside, Riverside, USA.

Orthopaedic Surgery, University of California Irvine School of Medicine, Irvine, USA.

出版信息

Cureus. 2022 Apr 19;14(4):e24275. doi: 10.7759/cureus.24275. eCollection 2022 Apr.

Abstract

Pycnodysostosis (PYCD) is an autosomal recessive lysosomal storage disorder of the bone which leads to stereotypical abnormalities consisting of, but not limited to, sclerotic and fragile bone, shortened distal phalanges, and obtuse mandibular angle. Current literature describes the otolaryngological manifestations and treatment of this disorder; however, the treatment of orthopedic fractures in PYCD patients is seldom described and remains a controversial topic. We aim to systematically review the current evidence regarding the optimal treatment of PYCD patients with fractures. We performed a literature search using PubMed, MEDLINE, Web of Science, and Google Scholar databases. Elig-ibility criteria consisted of English-language literature of PYCD patients undergoing treatment for orthopedic surgery fractures. Non-English papers or literature focused on maxillofacial manifestations/treatment were excluded. The database search resulted in the identification of 500 articles. After removing duplicates and enforcing our inclusion criteria, 29 case reports/series (40 patients) were included. The average age was 31.25 (-±18.2) years, with 57.5% of patients being female. Overall, 62.5% of patients had consanguineous parents. Additionally, 86.2% reported a history of previous fractures while 47.5% reported a spontaneous or minor trauma fracture, with most fractures occurring in the femur (60.0%) and tibia (40.0%). Radiographic features consisted of densification in the femur 45.0% (18/40), tibia 37.5% (15/40), and spine 25.0% (10/40). Overall, 84.2% of patients were treated with surgical management consisting of internal plate fixation (IPF) (48.3%), intramedullary fixation (20.7%), and Ilizarov external fixation (IEF) (13.8%). Overall, the refracture rate was 25.0% and was lowest in intramedullary fixation (0/6), compared to IPF (3/14) and IEF (3/4). Average time until refracture was 40.6 months (3-132 months). Long-term follow-up is recommended in patients with PYCD due to the propensity for fractures/refractures. While this study provides the groundwork for the treatment of PYCD patients, further research with higher-evidence studies should be conducted to establish the optimal orthopedic treatment of this disorder.

摘要

致密性骨发育不全(PYCD)是一种常染色体隐性遗传性溶酶体贮积性骨病,可导致一系列典型异常表现,包括但不限于骨质硬化且脆弱、远端指骨缩短以及下颌角钝圆。当前文献描述了该疾病的耳鼻喉科表现及治疗方法;然而,关于PYCD患者骨科骨折的治疗却鲜有描述,仍是一个存在争议的话题。我们旨在系统回顾目前有关PYCD骨折患者最佳治疗方法的证据。我们使用PubMed、MEDLINE、科学网和谷歌学术数据库进行了文献检索。纳入标准为有关接受骨科手术骨折治疗的PYCD患者的英文文献。排除非英文论文或聚焦于颌面表现/治疗的文献。数据库检索共识别出500篇文章。在去除重复文章并执行纳入标准后,纳入了29篇病例报告/系列研究(40例患者)。平均年龄为31.25(±18.2)岁,57.5%的患者为女性。总体而言,62.5%的患者父母为近亲结婚。此外,86.2%的患者有既往骨折史,47.5%的患者报告有自发性或轻微创伤性骨折,大多数骨折发生在股骨(60.0%)和胫骨(40.0%)。影像学特征包括股骨致密化45.0%(18/40)、胫骨致密化37.5%(15/40)和脊柱致密化25.0%(10/40)。总体而言,84.2%的患者接受了手术治疗,包括钢板内固定(IPF)(48.3%)、髓内固定(20.7%)和伊利扎罗夫外固定(IEF)(13.8%)。总体而言,再骨折率为25.0%,其中髓内固定的再骨折率最低(0/6),而钢板内固定为(3/14),伊利扎罗夫外固定为(3/4)。再骨折的平均时间为40.6个月(3 - 132个月)。由于PYCD患者有骨折/再骨折倾向,建议对其进行长期随访。虽然本研究为PYCD患者的治疗奠定了基础,但仍需开展更高证据水平的进一步研究,以确立该疾病的最佳骨科治疗方法。

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