Pediatric Orthopedics and Trauma Unit, Department of Orthopedic Surgery and Traumatology, La Fe University and Polytechnic Hospital of Valencia, Valencia, Spain.
Orthopadie (Heidelb). 2022 Dec;51(12):1010-1014. doi: 10.1007/s00132-022-04309-7. Epub 2022 Sep 26.
Pycnodysostosis is a rare autosomal recessive lysosomal disorder of bone characterized by diffuse skeletal condensation with thickening of the cortex and narrowing of the medullary canal.
We present the case of a 4-year-old girl diagnosed with pycnodysostosis and associated pathological tibial fracture. The tibia had an absence of medullary canal. Surgery included reduction and reaming of the canal with placement of a 5 mm diameter telescopic growing nail.
The presentation of pycnodysostosis as tibial fracture is rare and there is limited literature on its management. We showed its approach focusing mainly on the management of the absent medullary canal.
先天性骨生成不全症是一种罕见的常染色体隐性溶酶体骨病,其特征为弥漫性骨骼骨化,皮质增厚,骨髓腔变窄。
我们报告了一例 4 岁女孩患有先天性骨生成不全症和相关病理性胫骨骨折的病例。该胫骨缺乏骨髓腔。手术包括复位和扩髓,并置入 5 毫米直径的可延长生长钉。
先天性骨生成不全症表现为胫骨骨折较为罕见,其治疗方法的文献也有限。我们主要介绍了处理缺失的骨髓腔的方法。