Khalsa Amrit S, Kumar Neil S, Chin Matthew A, Lackman Richard D
Amrit S Khalsa, Neil S Kumar, Matthew A Chin, the Department of Orthopaedic Surgery, Hahnemann University Hospital, Philadelphia, PA 19102, United States.
World J Orthop. 2017 Jan 18;8(1):77-81. doi: 10.5312/wjo.v8.i1.77.
Dysplasia epiphysealis hemimelica (DEH), or Trevor's disease, is an osteocartilaginous epiphyseal overgrowth typically occurring in children. The literature reports 6 adult cases and none describe recurrence requiring additional procedures. We present a new-onset proximal tibial DEH in an adult recurring approximately 3 years after open excision. A 39-year-old female presented with a history of right knee pain, swelling, and instability. Physical examination revealed a firm proximal tibial mass. Computed tomography (CT) imaging showed an exophytic, lobulated, sclerotic mass involving the anterolateral margin of the lateral tibial plateau. Magnetic resonance imaging was suggestive of an osteochondroma. The patient underwent curettage of the lesion due to its periarticular location. Histology revealed benign and reactive bone and cartilage consistent with periosteal chondroma. Two and a half years later, the patient presented with a firm, palpable mass larger than the initial lesion. CT revealed a lateral tibial plateau sclerotic mass consistent with recurrent intra-articular DEH. A complete excision was performed and histology showed sclerotic bone with overlying cartilage consistent with exostosis. DEH is a rare epiphyseal osteocartilaginous outgrowth frequently occurring in the long bones of children less than 8 years old. DEH resembles an osteochondroma due to its pediatric presentation and similar histologic appearance. Adult-onset cases comprise less than 1% of reported cases. Recurrence rate after surgical intervention is unknown. Only 1 such case, occurring in a child, has been described. Clinicians contemplating operative treatment for DEH should note the potential for recurrence and consider complete excision. A follow-up period of several years may be warranted to identify recurrent lesions.
骨骺半侧发育异常(DEH),即特雷弗氏病,是一种通常发生于儿童的骨软骨性骨骺过度生长疾病。文献报道了6例成人病例,但均未描述需要额外手术的复发情况。我们报告了一例成人新发的胫骨近端DEH,在开放切除术后约3年复发。一名39岁女性因右膝疼痛、肿胀和不稳定前来就诊。体格检查发现胫骨近端有一坚实肿块。计算机断层扫描(CT)成像显示一个外生性、分叶状、硬化性肿块,累及胫骨外侧平台的前外侧边缘。磁共振成像提示为骨软骨瘤。由于病变位于关节周围,患者接受了病变刮除术。组织学检查显示为良性反应性骨和软骨,符合骨膜软骨瘤。两年半后,患者出现一个比最初病变更大、可触及的坚实肿块。CT显示胫骨外侧平台有一硬化性肿块,符合复发性关节内DEH。进行了完整切除,组织学检查显示硬化骨上覆盖软骨,符合外生骨疣。DEH是一种罕见的骨骺骨软骨性生长异常,常见于8岁以下儿童的长骨。由于其儿童期表现和相似的组织学外观,DEH类似于骨软骨瘤。成人发病病例占报告病例的不到1%。手术干预后的复发率未知。仅描述了1例发生在儿童的此类病例。考虑对DEH进行手术治疗的临床医生应注意复发的可能性,并考虑完整切除。可能需要数年的随访期以发现复发病变。