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致密性骨发育不全的骨折治疗:27年随访

Fracture management in pycnodysostosis: 27 years of follow-up.

作者信息

Bor Noam, Rubin Guy, Rozen Nimrod

机构信息

Department of Orthopaedic, Haemek Medical Center, Afula, Israel.

出版信息

J Pediatr Orthop B. 2011 Mar;20(2):97-101. doi: 10.1097/bpb.0b013e328341bc6a.

Abstract

Pycnodysostosis is a rare hereditary disease, characterized by systemic bone sclerosis, which is often brought to the orthopedic surgeon's attention because of repeated fractures. The operative treatment of the patient with a fracture is a real challenge for the orthopedic surgeon because of the unusual problems imposed by the hard but-brittle bone characteristics of the disease. We report a 27-year follow-up of a patient treated for fractures of both femurs and tibia with intramedullary nailing. According to our experience and literature review, we recommend the use of an internal fixation, preferably intramedullary nailing as the treatment of choice for these rare cases. Once the fractures are healed, the removal of the hardware is not recommended, as these keep the bones from further fractures.

摘要

致密性成骨不全症是一种罕见的遗传性疾病,其特征为全身性骨硬化,常因反复骨折而引起骨科医生的关注。由于该疾病坚硬但易碎的骨骼特性带来的特殊问题,骨折患者的手术治疗对骨科医生来说是一项真正的挑战。我们报告了一名接受股骨干和胫骨干骨折髓内钉治疗患者的27年随访情况。根据我们的经验和文献综述,我们建议使用内固定,最好是髓内钉,作为这些罕见病例的首选治疗方法。骨折愈合后,不建议取出内固定物,因为这些内固定物可防止骨骼再次骨折。

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