Department of Paediatric Orthopaedics, Fuzhou Second Hospital, The Third Clinical Medical College, Fujian Medical University, Fuzhou Second Hospital of Xiamen University, School of Medicine, Xiamen University, 47th Shangteng Road of Cangshan District, Fuzhou, 350007, Fujian Province, China.
Department of Paediatric Orthopaedic Surgery, Lille University Centre, Jeanne de Flandre Hospital, Rue Eugène Avinée, 59000, Lille, France.
Int Orthop. 2022 Dec;46(12):2877-2885. doi: 10.1007/s00264-022-05551-6. Epub 2022 Sep 10.
Ulna distraction by monolateral external fixator (MEFix) is a good option for the treatment of Masada type I and IIb deformities in children with hereditary multiple exostoses (HMEs). However, there is no consensus regarding where to perform ulnar osteotomy. Our hypothesis is that osteotomy at the proximal third of the ulna and progressive distraction with MEFix can simultaneously correct elbow and wrist deformities in patients with HME.
We retrospectively reviewed patients with HME who underwent ulna distraction osteogenesis from June 2014 to March 2019. The carrying angle (CA), radial articular angle (RAA), ulnar variance (UV), radial variance (RV) and range of motion (ROM) of the affected forearm and elbow were clinically assessed before lengthening and at the last follow-up visit. The total ulna lengthening distance (LD) and radiographic outcome were also recorded.
Nineteen patients (20 forearms) with HME aged 9.1 ± 2.4 years at the time of surgery were retrospectively reviewed. The mean follow-up period was 26.1 ± 5.6 months. There were 11 patients (12 forearms) with Masada type I deformities and eight patients (8 forearms) with Masada type IIb deformities. Patients with type IIb deformity had higher RV, lower CA values, less elbow flexion and forearm pronosupination than those with type I deformity (p < 0.05); RV was an independent risk factor for radial head dislocation, with the cut off at RV > 15.5 mm. The mean LDs in patients with type I and type IIb deformities were 33.6 ± 6.6 mm and 41.4 ± 5.4 mm, respectively. The mean CA, UV, RV, forearm pronation and ulna deviation at the wrist improved significantly following surgery in all patients. In particular, five of eight patients (62.5%) with type IIb deformities had concentric reduction of the radiocapitellar joint, while no radial head subluxation was detected in patients with type I deformities at the last follow-up. Three complications were recorded: two pin-track infections and one delayed union.
Distraction osteogenesis at the proximal third of the ulna provides satisfactory clinical and radiological outcomes in patients with Masada type I and IIb deformities. Early treatment of Masada type I deformities is indicated before progression to more complex type IIb deformities.
单侧外固定架(MEFix)下尺骨延长术是治疗遗传性多发性外生骨疣(HME)儿童 Masada Ⅰ型和Ⅱb 型畸形的一种较好选择。然而,对于尺骨截骨部位仍未达成共识。我们的假设是尺骨近 1/3 处截骨并使用 MEFix 进行逐渐延长,可以同时矫正 HME 患者的肘部和腕部畸形。
我们回顾性分析了 2014 年 6 月至 2019 年 3 月期间接受尺骨延长的 HME 患者。在延长前和末次随访时,对受累前臂和肘部的提携角(CA)、桡腕关节角(RAA)、尺骨变异(UV)、桡骨变异(RV)和活动范围(ROM)进行临床评估。同时记录总的尺骨延长距离(LD)和影像学结果。
共回顾了 19 例(20 侧)HME 患者,手术时年龄为 9.1±2.4 岁。平均随访时间为 26.1±5.6 个月。其中 11 例(12 侧)为 Masada Ⅰ型畸形,8 例(8 侧)为 Masada Ⅱb 型畸形。Ⅱb 型畸形患者的 RV 更高,CA 值更低,肘部屈曲和前臂旋前旋后角度更小(p<0.05);RV 是桡骨头脱位的独立危险因素,其截断值为 RV>15.5mm。Ⅰ型和Ⅱb 型畸形患者的平均 LD 分别为 33.6±6.6mm 和 41.4±5.4mm。所有患者术后 CA、UV、RV、前臂旋前和腕部尺偏均显著改善。特别是 8 例Ⅱb 型畸形患者中有 5 例(62.5%)桡尺骨小头关节达到同心复位,而Ⅰ型畸形患者在末次随访时未发现桡骨头半脱位。记录到 3 例并发症:2 例针道感染,1 例延迟愈合。
尺骨近 1/3 处的延长术为 Masada Ⅰ型和Ⅱb 型畸形患者提供了满意的临床和影像学结果。在进展为更复杂的Ⅱb 型畸形之前,应早期治疗 Masada Ⅰ型畸形。