Trehan R K, Dabbas N, Allwood D, Agarwal M, Kinmont C
Trauma and Orthopaedics, Kingston Hospital, Surrey, UK.
J Med Case Rep. 2008 May 22;2:172. doi: 10.1186/1752-1947-2-172.
Multiple epiphyseal dysplasia is a genetically and clinically heterogeneous osteochondroplasia with symmetrical involvement. It is characterized by joint pain in childhood and early adulthood with early onset of osteoarthritis, mainly affecting the hips.
We report the case of a 20-year-old man of Asian origin with multiple epiphyseal dysplasia presenting with bilateral knee pain, stiffness and instability found to be caused by bilateral anterior cruciate ligament impingement on abnormal medial femoral condyles. Bilateral staged arthroscopic notchplasty was performed successfully, resulting in subjective relief of pain, and improved range of movement and stability.
Care should be taken not to exclude a diagnosis of multiple epiphyseal dysplasia when few of the characteristic radiographic features are evident but clinical suspicion is high. This case highlights the scope for subjective symptomatic improvement following a minimum of surgical intervention. We recommend limiting early intervention to managing symptomatic features rather than radiographic abnormalities alone.
多发性骨骺发育不良是一种具有遗传和临床异质性的骨软骨发育不良,呈对称性累及。其特征为儿童期和成年早期出现关节疼痛,并早期发生骨关节炎,主要影响髋关节。
我们报告了一例20岁的亚洲裔男性患有多发性骨骺发育不良,表现为双侧膝关节疼痛、僵硬和不稳定,经检查发现是双侧前交叉韧带受到异常内侧股骨髁的撞击所致。成功进行了双侧分期关节镜下切迹成形术,使患者主观疼痛缓解,活动范围和稳定性得到改善。
当特征性影像学表现不明显但临床怀疑度高时,应注意不要排除多发性骨骺发育不良的诊断。本病例突出了最少手术干预后主观症状改善的可能性。我们建议早期干预应限于处理症状性特征,而不仅仅是影像学异常。