Yang G, Feng X H, Zhao W H, Tan Q, Liu K, Hu X K, Mo S S, Xie Y H, Mei H B, Zhu G H
Department of Orthopedics, the Children's Hospital Affiliated to Xiangya School of Medicine, Central South University (Hunan Children's Hospital), Key Laboratory of Pediatric Orthopedics of Hunan Province, Changsha 417000, China.
Zhonghua Wai Ke Za Zhi. 2024 Sep 1;62(9):864-869. doi: 10.3760/cma.j.cn112139-20240328-00150.
To investigate the clinical and radiologic characteristics of children with congenital pseudarthrosis of the tibia (CPT) in a single center. 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 test or tests. 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) . 66.2%(104/157);=9.24, =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) (=8.33, =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 .(2.1±1.8)times;=14.93,<0.01). 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.
在单一中心研究先天性胫骨假关节(CPT)患儿的临床和影像学特征。这是一项回顾性病例系列研究。根据纳入和排除标准,收集了2011年1月至2020年12月在中南大学湘雅医学院附属儿童医院骨科接受治疗的497例CPT患儿(507条肢体)的临床资料。基线数据包括性别、初诊年龄、症状出现年龄、伴随症状、居住地、是否首次在我院治疗以及手术或保守治疗等治疗相关信息、手术并发症等,使用健康信息系统进行提取和分析。使用图像存档和通信系统分析患儿的影像学数据,包括克劳福德分类、双侧腿长、腓骨假关节的存在情况以及胫骨节段假关节的位置。数据采用独立样本检验或检验进行比较。在497例CPT患儿中,男性305例(61.4%),女性192例(38.6%)。初诊年龄为(3.6±3.2)岁(范围:0.1至16.2岁)。1型神经纤维瘤病(NF1)症状在340例患儿中呈阳性(68.4%),在157例患儿中呈阴性(31.6%)。在NF1阳性患儿中,症状在1岁前出现的患儿明显多于NF1阴性患儿(74.1%(252/340)对66.2%(104/157);=9.24,=0.001),骨折比例(92.9%,316/340)明显高于NF1阴性组(84.7%,133/157)(=8.33,=0.004)。根据影像学数据,克劳福德Ⅳ型是最常见的类型,有321条肢体(63.3%),其次是Ⅱ型100条肢体(19.7%),Ⅲ型54条肢体(10.7%),Ⅰ型32条肢体(6.3%)。假关节发生在胫骨近端三分之一处14条肢体(2.8%),中部三分之一处185条肢体(36.5%),远端三分之一处308条肢体(60.8%)。74例患儿(14.9%)伴有腓骨假关节。胫骨近端外侧角为86.91°±5.21°(范围:72.17°至102.08°),胫骨远端外侧角为87.27°±10.73°(范围:51.07°至128.17°)。共有421例患儿(84.7%)接受了手术治疗,每名患儿平均进行(3.1±2.4)次手术(范围:0至12次手术);76例患儿(15.3%)接受了保守治疗。术后并发症主要包括踝外翻(77例)、腿长差异(71例)、再骨折(48例)、骨髓炎(11例)和内固定失败(10例)。NF1阳性患儿比NF1阴性患儿接受的手术更多((5.1±2.2)次对(2.1±1.8)次;=14.93,<0.01)。在本研究中,克劳福德Ⅳ型是儿童CPT最常见的类型。CPT主要发生在胫骨的中三分之一或远三分之一处。大多数CPT患儿在3岁前出现症状并到门诊就诊。目前与CPT治疗相关主要手术并发症是踝外翻和腿长差异。与无NF1的CPT患儿相比,NF1阳性CPT患儿往往症状出现更早,可能需要更频繁的治疗。