Segal Lee S, Crandall Robin C
Division of Pediatric Orthopaedics, Phoenix Children's Hospital, Phoenix, AZ 85016, USA.
J Pediatr Orthop. 2009 Mar;29(2):120-3. doi: 10.1097/BPO.0b013e3181982c15.
Progressive varus deformity of the tibia in pediatric patients after transtibial and Syme amputations has not been reported in a series. A distal tibia to fibula synostosis, created surgically to minimize the risk of terminal overgrowth or occurring spontaneously, was noted in most patients. The goals of this study are to address the causes of the deformity, the implications for prosthetic wear, and potential treatment options.
Twelve patients identified from the juvenile amputee database at 2 centers developed progressive varus deformity of the residual limb. One patient had bilateral involvement. A distal tibia-fibula synostosis was noted in 12 (92%) of the residual limbs, and in one, a fibrous union was suspected. The level of amputation was trans-tibial in 10 patients, and Syme amputation in 3 patients. Two patients had acquired trans-tibial level of amputation from congenital constriction band syndrome. Nine of the patients (75%) were between the ages of 3 and 5 years at the time of injury.
The mean proximal medial tibial angle was 80.5 degrees (range, 75-85 degrees). Ten of the patients underwent procedures to correct the mechanical axis and resolve or prevent problems with prosthetic fitting. Four patients has proximal tibial osteotomies (HTO), 2 oblique closing wedge osteotomies, 1 shaft osteotomy, and 4 lateral proximal tibial hemi-epiphyseodesis. In 2 patients, no correction was recommended.
The presence of a distal tibia-fibula synostosis in pediatric amputee patients may contribute to the risk of developing a progressive varus deformity and should be monitored during a child's growth. Distal tibiofibular synostosis may disrupt normal differential longitudinal growth and may contribute to this progressive angular deformity. Severe deformity may require prosthetic modifications or operative correction to provide for a normal mechanical axis. Lateral hemiepiphyseodesis of the proximal tibia can be effective if the deformity is detected early. We do not recommend creation of a synostosis in the young child for terminal growth.
Level 4.
小儿经胫骨截肢和赛姆截肢术后胫骨渐进性内翻畸形尚未有系列报道。多数患者可见通过手术形成的胫腓骨远端融合,以降低末端过度生长的风险,或为自然形成。本研究的目的是探讨畸形的成因、对假肢穿戴的影响以及潜在的治疗方案。
从2个中心的青少年截肢者数据库中确定的12例患者出现了残肢渐进性内翻畸形。1例患者双侧受累。12条(92%)残肢发现胫腓骨远端融合,1例疑似纤维性连接。截肢平面为经胫骨截肢10例,赛姆截肢3例。2例患者因先天性束带综合征导致经胫骨平面截肢。9例患者(75%)受伤时年龄在3至5岁之间。
胫骨近端内侧平均角度为80.5度(范围75 - 85度)。10例患者接受了纠正机械轴和解决或预防假肢适配问题的手术。4例患者行胫骨近端截骨术(HTO),2例斜行闭合楔形截骨术,1例骨干截骨术,4例胫骨近端外侧半骨骺阻滞术。2例患者未建议进行矫正。
小儿截肢患者存在胫腓骨远端融合可能会增加发生渐进性内翻畸形的风险,在儿童生长过程中应予以监测。胫腓骨远端融合可能会破坏正常的差异纵向生长,并可能导致这种渐进性角畸形。严重畸形可能需要假肢调整或手术矫正以提供正常的机械轴。如果畸形早期被发现,胫骨近端外侧半骨骺阻滞术可能有效。我们不建议为防止末端生长而在幼儿中形成融合。
4级。