Kitamura Takaki, Yamazaki Shuji, Kijima Takehiro, Takamori Yasuyuki, Watanabe Eiichiro
Department of Orthopaedic Surgery, Chiba University, Graduate School of Medicine, Chiba, JPN.
Department of Orthopaedic Surgery, Fuji Orthopaedic Hospital, Fuji, JPN.
Cureus. 2024 Apr 24;16(4):e58906. doi: 10.7759/cureus.58906. eCollection 2024 Apr.
Multiple epiphyseal dysplasia (MED) is a congenital disease causing epiphyseal dysplasia in long bones. Herein, we report a case of a middle-aged man with bilateral knee joint locking symptoms who was diagnosed with multiple epiphyseal dysplasia caused by Matrilin-3 (MATN3) pathogenic variants and was successfully treated with arthroscopic loose body removal. A 48-year-old man has had bilateral knee pain since his twenties and underwent loose body removal of both knees in his thirties. He visited our hospital for worsening locking symptoms in both knees. Twenty years ago, his son had been diagnosed with suspected multiple epiphyseal dysplasia. Genetic and imaging testing confirmed his diagnosis of multiple epiphyseal dysplasia due to Matrilin-3 pathogenic variants. Arthroscopic loose body removal was performed, and the locking symptoms disappeared after surgery. Arthroscopic loose body removal was effective for the locking symptoms in a mild adult case of multiple epiphyseal dysplasias caused by Matrilin-3 pathogenic variants.
多发性骨骺发育不良(MED)是一种导致长骨骨骺发育异常的先天性疾病。在此,我们报告一例中年男性,其双侧膝关节出现交锁症状,被诊断为由基质金属蛋白酶-3(MATN3)致病变异引起的多发性骨骺发育不良,并通过关节镜下取出游离体成功治愈。一名48岁男性自二十多岁起就出现双侧膝关节疼痛,三十多岁时接受了双侧膝关节游离体取出术。他因双侧膝关节交锁症状加重前来我院就诊。二十年前,他的儿子被诊断为疑似多发性骨骺发育不良。基因和影像学检查证实他因基质金属蛋白酶-3致病变异而诊断为多发性骨骺发育不良。进行了关节镜下游离体取出术,术后交锁症状消失。关节镜下取出游离体对由基质金属蛋白酶-3致病变异引起的轻度成人多发性骨骺发育不良的交锁症状有效。