Gökkuş Kemal, Atmaca Halil, Sagtas Ergin, Saylik Murat, Aydin Ahmet T
Departments of aOrthopaedics and Trauma bRadiodiagnostic, Antalya Memorial Hospital cOrthopaedics and Trauma Department, Akdeniz University School of Medicine, Antalya dOrthopaedics and Trauma Department, Ozel Bahar Hospital, Bursa, Turkey.
J Pediatr Orthop B. 2017 Nov;26(6):532-545. doi: 10.1097/BPB.0000000000000269.
Trevor's disease, also known as dysplasia epiphysealis hemimelica, is a rare nonhereditary skeletal development disorder that affects epiphyses. This type of dysplastic lesion was first reported by Mouchet and Berlot in 1926 under the name 'tarsomegaly'. The main aim of this study is to raise awareness of Trevor's disease among orthopedic surgeons and underline some important aspects of treatment by a detailed presentation of four different possible manifestations of the disease. Four different treatment methods were used on four different patients (three localized in hindfoot ankle region and one classic Trevor's disease case). Treatment methods, localization of the sides involved, different characteristics of entire lower extremity, asymetry, distal femoral lateral epiphysis involvement, and hip involvement were analyzed thoroughly and the results were compared with those found in the most recent literature. Of our four patients, three were localized (hind foot ankle) cases and one was a classic dysplasia epiphysealis hemimelica with hemimelic distribution of the entire lower extremity. We used arthroscopic resection, observation, excision, and temporary hemiepiphysiodesis treatment methods in each of our cases. Clinical follow-up results were reported to be between good and excellent. In sum, our opinion is that the treatment for this condition should be customized according to lesion localization and lesion size. Majority of cases with ankle involvement show good prognosis following excision. Observation is also an alternative in patients who refuse surgery. If an intra-articular lesion is present, the surgeon should perform an arthroscopy for assessment of lesion surface. If the lesion is adapted to the joint curvature, it should be left alone and hemiepiphysiodesis should be considered for correction. The most risky involvements that are related to deformities and limb-length discrepancies are the hip and the knee. This is usually the result of corrective osteotomy targeted at the supracondylar femoral area in immature skeletons. Hemiepiphysiodesis might be a more feasible option in those cases as it provides the surgeon with the choice to remove the staples when necessary.
特雷弗氏病,又称半侧肢体骨骺发育异常,是一种罕见的非遗传性骨骼发育障碍,会影响骨骺。这种发育异常性病变最早由穆谢和贝洛于1926年以“跗骨巨大症”之名报道。本研究的主要目的是提高骨科医生对特雷弗氏病的认识,并通过详细介绍该疾病四种不同的可能表现形式来强调一些重要的治疗方面。对四名不同患者采用了四种不同的治疗方法(三例局限于后足踝区域,一例为典型的特雷弗氏病病例)。对治疗方法、受累侧别定位、整个下肢的不同特征、不对称性、股骨远端外侧骨骺受累情况以及髋关节受累情况进行了全面分析,并将结果与最新文献中的结果进行了比较。我们的四名患者中,三例为局限性(后足踝)病例,一例为典型的半侧肢体骨骺发育异常,整个下肢呈半侧肢体分布。我们在每个病例中分别采用了关节镜下切除、观察、切除和临时半骨骺阻滞治疗方法。临床随访结果显示良好至优秀。总之,我们认为这种疾病的治疗应根据病变定位和病变大小进行定制。大多数踝关节受累病例切除后预后良好。对于拒绝手术的患者,观察也是一种选择。如果存在关节内病变,外科医生应进行关节镜检查以评估病变表面。如果病变与关节曲度相适应,则应不予处理,并应考虑采用半骨骺阻滞进行矫正。与畸形和肢体长度差异相关的最危险受累部位是髋关节和膝关节。这通常是针对未成熟骨骼的股骨髁上区域进行矫正截骨术的结果。在这些病例中,半骨骺阻滞可能是一种更可行的选择,因为它为外科医生提供了在必要时取出固定钉的选择。