[The clinical characteristics of 497 children with congenital pseudarthrosis of the tibia]

Zhonghua Wai Ke Za Zhi. 2024 Sep 1;62(9):864-869. doi: 10.3760/cma.j.cn112139-20240328-00150.
[Article in Chinese]

Abstract

Objective: To investigate the clinical and radiologic characteristics of children with congenital pseudarthrosis of the tibia (CPT) in a single center. Methods: This is a retrospective case series study. According to inclusion and exclusion criteria, clinical data of 497 children(507 limbs) with CPT who were treated at Department of Orthopedics, the Children's Hospital Affiliated to Xiangya School of Medicine, Central South University from January 2011 to December 2020 were collected. Baseline data included gender, age at initial visit, age at onset of symptoms, accompanying symptoms, domicile, whether first treated at our hospital, and treatment-related information such as surgical or conservative treatment, surgical complications, etc., were extracted and analyzed using the health information system. Imaging data of the children, including Crawford classification, bilateral leg lengths, presence of fibular pseudarthrosis, and location of pseudarthrosis along the tibia segment, were analyzed using the Picture Archiving and Communication System. Data were compared using independent sample t test or χ2 tests. Results: Among 497 children with CPT, there were 305 males (61.4%) and 192 females (38.6%). The age at initial visit was (3.6±3.2) years (range: 0.1 to 16.2 years). Neurofibromatosis type 1 (NF1) symptoms were positive in 340 children (68.4%), and negative in 157 children (31.6%). Among NF1-positive children, those with symptoms onset before 1 year of age were significantly more than NF1-negative children (74.1%(252/340) vs. 66.2%(104/157);χ2=9.24, P=0.001), and the proportion of fractures (92.9%,316/340) was significantly higher than that in the NF1-negative group (84.7%,133/157) (χ2=8.33, P=0.004). According to imaging data, Crawford type Ⅳ was the most common type, with 321 limbs (63.3%), followed by type Ⅱ in 100 limbs (19.7%), type Ⅲ in 54 limbs (10.7%) and type Ⅰ in 32 limbs (6.3%). Pseudarthrosis occurred in the proximal third of the tibia in 14 limbs (2.8%), in the middle third in 185 limbs (36.5%), and in the distal third in 308 limbs (60.8%). Seventy-four children (14.9 %) had associated fibular pseudarthrosis. The lateral proximal tibial angle was 86.91°±5.21°(range: 72.17° to 102.08°), and the lateral distal tibial angle was 87.27°±10.73°(range: 51.07° to 128.17°). A total of 421 children (84.7%) underwent surgical treatment with (3.1±2.4) surgeries performed per child (range:0 to 12 surgeries); 76 children (15.3%) received conservative treatment. Postoperative complications mainly included ankle valgus (77 cases), leg length discrepancy (71 cases),refracture (48 cases), osteomyelitis (11 cases), and hardware failure (10 cases). NF1-positive children underwent more surgeries than NF1-negative children ((5.1±2.2)times vs.(2.1±1.8)times;t=14.93,P<0.01). Conclusions: Crawford type Ⅳ is the most common type of CPT in children in this study. CPT predominantly occurs in the middle or distal third of the tibia. The majority of children with CPT experienced symptoms and were seen at outpatient clinics before the age of 3 years. The main surgical complications currently associated with CPT treatment are ankle valgus and leg length discrepancy. Compared with CPT without NF1, children with NF1-positive CPT tend to have earlier symptom onset and may require more frequent treatments.

目的: 探讨单中心先天性胫骨假关节(CPT)患儿的临床和影像学特征。 方法: 本研究为回顾性病例系列研究。根据纳入标准和排除标准,收集2011年1月至2020年12月于中南大学湘雅医学院附属儿童医院就诊的497例(507条患肢)CPT患儿的临床资料。利用健康信息系统提取并分析患儿的基线资料,包括性别、首诊年龄、首次出现症状年龄、合并症、户籍地等;以及治疗相关资料,包括手术或保守治疗情况、手术相关并发症等。通过影像存档与传输系统提取并分析患儿影像学资料,包括Crawford分型、双下肢长度差异、是否伴有腓骨假关节以及假关节对应的胫骨的节段。数据比较采用独立样本t检验或χ2检验。 结果: 497例CPT患儿中,男305例(61.4%),女192例(38.6%),首次入院年龄(3.6±3.2)岁(范围:0.1~16.2岁)。合并神经纤维瘤病1型(NF1)患儿340例(68.4%),非NF1患儿157例(31.6%)。在合并NF1的患儿中,首发症状出现在1岁以内[74.1%(252/340)比66.2%(104/157),χ2=9.24,P=0.001]和发生骨折的比例[92.9%(316/340)比84.7%(133/157),χ2=8.33,P=0.004]明显高于不合并NF1患儿。影像学资料显示,507条患肢中Crawford Ⅳ型最多,共321例次(63.3%),其次为Crawford Ⅱ型100例次(19.7%)、Crawford Ⅲ型54例次(10.7%)和Crawford Ⅰ型32例次(6.3%)。CPT发生于胫骨近端1/3处14例次(2.8%),中段1/3处185例次(36.5%),远端1/3处308例次(60.8%)。合并腓骨假关节的患儿74例(14.9%)。胫骨近端外侧角为86.91°±5.21°(范围:72.17°~102.08°),胫骨远端外侧角为87.27°±10.73°(范围:51.07°~128.17°)。421例(84.7%)患儿接受了手术治疗,在我科手术次数为(3.1±2.4)次(范围:0~12次);76例(15.3%)患儿接受了保守治疗。手术并发症包括踝关节外翻77例、双下肢不等长71例、再骨折48例、骨髓炎11例、内固定物断裂10例。合并NF1患儿的手术次数多于不合并NF1患儿[(5.1±2.2)次比(2.1±1.8)次;t=14.93,P<0.01]。 结论: 本组CPT患儿中Crawford Ⅳ型比例最高,且多见于胫骨中段或远端1/3。多数患儿的首次出现症状年龄在3岁以内。CPT手术治疗后的主要并发症为踝关节外翻和双下肢不等长;合并NF1的CPT患儿的首发症状更早且可能需要接受更多次手术治疗。.

Publication types

  • English Abstract

MeSH terms

  • Child
  • Child, Preschool
  • Female
  • Humans
  • Infant
  • Male
  • Pseudarthrosis* / congenital
  • Pseudarthrosis* / diagnosis
  • Retrospective Studies
  • Tibia* / abnormalities
  • Tibia* / surgery

Supplementary concepts

  • Congenital pseudoarthrosis