Westberry David E, Carpenter Ashley M, Barrera John, Westberry Alison
Shriners Hospitals for Children.
University of South Carolina School of Medicine, Greenville.
J Pediatr Orthop. 2020 Apr;40(4):203-209. doi: 10.1097/BPO.0000000000001182.
Deformity of the tibia, including shortening and angulation, may accompany severe forms of postaxial hypoplasia (fibular deficiency). The current literature reflects varying opinions on the appropriate management for tibial deformity in the setting of fibular deficiency.
We performed a retrospective review to determine outcomes of tibial deformity correction in patients with a primary diagnosis of fibular deficiency. Clinical and radiographic outcomes of patients treated with foot ablation were reviewed to establish indications for tibial deformity correction, identify occurrence of additional surgical procedures related to limb alignment or deformity, and characterize difficulties with prosthetic wear potentially related to residual or recurrent tibial deformity.
From 1989 to 2016, 51 patients (57 extremities) with fibular deficiency were managed with a foot ablation procedure. Twenty-five (44%) had simultaneous correction of the tibial deformity. The initial tibial deformity measured 42.5 degrees, was corrected to 5.6 degrees intraoperatively, and measured 18.6 degrees at follow-up, suggesting recurrent deformity. In follow-up, approximately half of the patients complained of redness and one third complained of a continued prominence along the anterior tibia. Thirty-two extremities had an isolated foot ablation procedure without tibial osteotomy. Radiographic review demonstrated mild tibial bowing at the time of amputation with a mean angular deformity of 15.4 degrees and remained unchanged during the follow-up period (mean, 12.7 degrees). Similar to the osteotomy group, approximately half of the patients complained of redness and erythema over the anterior bow, with one fourth noting prominence, and only 2 reporting significant pain.
Tibial osteotomies in patients with more significant degrees of angular deformity can be safely performed at the same setting as foot ablative procedures for fibular deficiency. Recurrent deformity with growth may occur. Patients and their caregivers should be aware that rebound deformity may occur, but typically can be managed with prosthetic adjustment and without significant disruption to the child's daily activities.
Level IV (case series).
胫骨畸形,包括短缩和成角,可能伴随严重形式的轴后发育不全(腓骨缺如)。当前文献对于腓骨缺如情况下胫骨畸形的合适治疗方法存在不同观点。
我们进行了一项回顾性研究,以确定初步诊断为腓骨缺如患者的胫骨畸形矫正结果。对接受足部截肢治疗患者的临床和影像学结果进行了回顾,以确定胫骨畸形矫正的指征,识别与肢体对线或畸形相关的额外手术操作的发生情况,并描述可能与残留或复发性胫骨畸形相关的假肢穿戴困难。
1989年至2016年,51例(57个肢体)腓骨缺如患者接受了足部截肢手术。25例(44%)同时进行了胫骨畸形矫正。初始胫骨畸形为42.5度,术中矫正至5.6度,随访时为18.6度,提示畸形复发。随访中,约一半患者抱怨发红,三分之一患者抱怨胫骨前部持续突出。32个肢体仅进行了足部截肢手术,未行胫骨截骨术。影像学检查显示截肢时胫骨轻度弓形,平均角畸形为15.4度,随访期间保持不变(平均为12.7度)。与截骨术组类似,约一半患者抱怨弓形前部发红和红斑,四分之一患者指出有突出,只有2例报告有明显疼痛。
对于角畸形程度更严重的腓骨缺如患者,胫骨截骨术可在与足部截肢手术相同的情况下安全进行。随着生长可能会出现畸形复发。患者及其护理人员应意识到可能会出现反弹畸形,但通常可通过假肢调整进行处理,且不会对儿童日常活动造成重大干扰。
IV级(病例系列)。