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先天性胫骨假关节:非典型近段位置。

Congenital pseudarthrosis of the tibia: an atypical proximal location.

机构信息

Service d'orthopédie traumatologie, hôpital de la Pitié-Salpêtrière, 47-83, boulevard de l'Hôpital, 75013 Paris, France.

出版信息

Orthop Traumatol Surg Res. 2010 Feb;96(1):70-4. doi: 10.1016/j.rcot.2009.12.008.

Abstract

UNLABELLED

Proximal location of congenital pseudarthrosis of the tibia (CPT) is uncommon, and its management challenging, risking to end in amputation. We here report a case of proximal CPT managed in a limb-sparing perspective and followed up until the end of growth. A 17-year-old girl presented with type-1 neurofibromatosis and proximal CPT. Initial X-ray showed severe pseudarthrosis of the tibia with bone atrophy, 12-cm shortening and femorotibial and femoropatellar dislocation. Inter-tibiofibular graft and fibular tibialization were performed. At end of follow-up (age 33 years), fusion had been obtained. For orthoprosthetic and cosmetic reasons, a Boyd amputation of the tarsus was performed when the patient was 22 years of age. The functional result was very good, with 0-100 degrees knee mobility. CPT, when proximal, completely disorganizes the knee joint, which is otherwise usually unaffected by this pathology. To achieve a good result, a limb-sparing treatment should combine correction of the tibial axis and of the dislocation of the knee, fibula osteosynthesis and bone graft.

LEVEL OF EVIDENCE

Level IV retrospective

摘要

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先天性胫骨假关节(CPT)近端位置不常见,其治疗具有挑战性,有截肢的风险。我们在此报告一例采用保肢治疗并随访至生长结束的近端 CPT 病例。一名 17 岁女孩患有 1 型神经纤维瘤病和近端 CPT。初始 X 线片显示胫骨严重假关节,伴有骨萎缩、12cm 缩短以及股骨-胫骨和股骨-髌骨关节脱位。进行了胫腓骨间移植和腓骨胫骨化。在随访结束时(33 岁),已获得融合。出于矫形和美容原因,患者 22 岁时进行了 Boyd 踝关节离断术。功能结果非常好,膝关节活动度为 0-100 度。CPT 近端完全扰乱膝关节,而膝关节通常不受该病理影响。为了获得良好的结果,保肢治疗应结合胫骨轴线和膝关节脱位的矫正、腓骨骨固定和植骨。

证据水平

IV 级回顾性

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