Department of Orthopedic Surgery, Seoul National University College of Medicine, Seoul, South Korea.
J Bone Joint Surg Am. 2010 May;92(5):1137-43. doi: 10.2106/JBJS.I.00876.
A solitary osteochondroma of the finger occasionally occurs intra-articularly and may cause clinical symptoms, including limited motion and deformity. The present report describes the clinical features and the results of operative treatment for a series of patients who had a solitary intra-articular osteochondroma of the finger.
Ten patients with a solitary intra-articular osteochondroma of a phalanx of a finger were managed surgically. Eight patients were male, and two were female. The average age at the time of surgery was fourteen years. Treatment consisted of mass excision for three patients and mass excision with corrective osteotomy for six. One additional patient had a boutonniere deformity and underwent extensor tendon reconstruction combined with mass excision. The average duration of follow-up was forty-four months.
The proximal phalanx was affected in six patients, and the middle phalanx was affected in four. All tumors involved the distal epiphysis. All patients had postoperative improvement in terms of deformity and/or limitation of motion. Six patients had a preoperative mean coronal plane deformity of 29 degrees, which improved to 4 degrees after surgery. The preoperative mean arc of flexion-extension improved from 54 degrees to 78 degrees in four patients who had a motion deficit at the proximal interphalangeal joint and from 60 degrees to 80 degrees in one patient who had a motion deficit at the distal interphalangeal joint. Two patients had a residual flexion contracture, one with preexisting osteoarthritis and one with a longstanding progressive boutonniere deformity. There were no other complications or recurrences.
Isolated intra-articular osteochondroma of the finger can cause deformity and/or motion limitation. Early mass excision and corrective osteotomy when indicated are recommended to restore full range of motion and to prevent osteoarthritis and secondary deformity.
手指的孤立性骨软骨瘤偶尔会发生在关节内,并可能引起临床症状,包括运动受限和畸形。本报告描述了一组手指关节内孤立性骨软骨瘤患者的临床特征和手术治疗结果。
对 10 例手指关节内孤立性骨软骨瘤患者进行手术治疗。8 例为男性,2 例为女性。手术时的平均年龄为 14 岁。治疗方法包括 3 例肿块切除术和 6 例肿块切除术联合矫正性截骨术。另有 1 例患者有纽扣畸形,行伸肌腱重建术联合肿块切除术。平均随访时间为 44 个月。
6 例患者的近节指骨受累,4 例患者的中节指骨受累。所有肿瘤均累及远节骺。所有患者术后在畸形和/或运动受限方面均有改善。6 例患者术前冠状面平均畸形为 29 度,术后改善至 4 度。4 例近侧指间关节运动受限患者术前屈伸弧从 54 度改善至 78 度,1 例远侧指间关节运动受限患者从 60 度改善至 80 度。2 例患者有残余屈曲挛缩,1 例有术前骨关节炎,1 例有长期进行性纽扣畸形。无其他并发症或复发。
手指关节内孤立性骨软骨瘤可引起畸形和/或运动受限。建议早期切除肿块和矫正性截骨,以恢复完全的运动范围,并预防骨关节炎和继发性畸形。