J Am Acad Orthop Surg. 2014 Apr;22(4):246-55. doi: 10.5435/JAAOS-22-04-246.
Congenital fibular deficiency (CFD) is characterized by a wide spectrum of manifestations ranging from mild limb length inequality (LLI) to severe shortening, with foot and ankle deformities and associated anomalies. The etiology of CFD remains unclear. Treatment goals are to achieve normal weight bearing, a functional plantigrade foot, and equal limb length. The recent Birch classification system has been proposed to provide a treatment guide: the functionality of the foot, LLI, and associated anomalies should be taken into account for decision-making. Treatment options include orthosis or epiphysiodesis, Syme or Boyd amputation and prosthetic rehabilitation, limb lengthening procedures, and foot and ankle reconstruction. The outcome of amputation for severe forms of CFD has shown favorable results and fewer complications compared with those of limb lengthening. Nevertheless, advances in the limb lengthening techniques may change our approach to treating patients with CFD and might extend the indications for reconstructive procedures to the treatment of severe LLI and foot deformities.
先天性腓骨发育不全(CFD)的临床表现范围广泛,从轻度肢体长度不等(LLI)到严重缩短,伴有足部和踝关节畸形及相关异常。CFD 的病因仍不清楚。治疗目标是实现正常承重、功能跖行足和肢体等长。最近提出了 Birch 分类系统,以提供治疗指南:应考虑足部功能、LLI 和相关异常来做出决策。治疗选择包括矫形器或骺板切除术、Syme 或 Boyd 截肢和假肢康复、肢体延长术以及足踝重建。与肢体延长术相比,严重 CFD 形式的截肢的结果显示出更好的结果和更少的并发症。然而,肢体延长技术的进步可能会改变我们治疗 CFD 患者的方法,并可能将重建手术的适应证扩展到严重 LLI 和足部畸形的治疗。