Gottschalk Hilton P, Bednar Michael S, Moor Molly, Light Terry R
Department of Orthopaedic Surgery and Rehabilitation, Loyola University Medical Center, Maywood, IL, USA.
J Hand Surg Am. 2012 Oct;37(10):2074-81. doi: 10.1016/j.jhsa.2012.06.021. Epub 2012 Sep 5.
To describe a case series of congenital metacarpal synostosis treated with longitudinal osteotomy and bone graft substitute interposition.
We retrospectively reviewed charts of all patients with metacarpal synostosis treated with a longitudinal osteotomy and bone graft substitute interposition at 2 institutions. Radiographic and clinical appearances were analyzed at initial diagnosis, intraoperatively, and at last follow-up.
A total of 10 patients (14 hands) met the inclusion criteria. Six patients (8 hands) demonstrated ring-little finger metacarpal synostosis and 4 patients (6 hands) had a middle-ring finger metacarpal synostosis. The median age at operation was 5 years (range, 2-16 y). Follow-up ranged from 1 to 14 years (average, 3 y). Associated hand anomalies included polydactyly, symbrachydactyly, and clinodactyly. Before surgery, the little finger proximal phalanx was angulated away from the middle finger metacarpal on average 46° (range, 26°-60°), and the angulation between the middle and the ring fingers averaged 43° (range, 26°-50°). Postoperative correction at 1 year was statistically significant for both ring-little finger metacarpal synostosis, average 23° (range, 10°-30°), and middle-ring finger metacarpal synostosis, average 16° (range, 5°-44°). Recurrence of digital abduction was evident in 2 patients who had middle-ring finger metacarpal synostosis.
Metacarpal synostosis is an uncommon congenital hand anomaly characterized by the coalescence of 2 adjacent metacarpals. In the most common form, the ring and little finger metacarpals are associated with abduction of the small finger in an awkward position. Use of the described technique is safe and effective, yet concerns remain regarding mild persistent angulation and risk of recurrence.
Congenital metacarpal synostosis may be effectively treated with a longitudinal osteotomy, realignment of component metacarpals, and interposition of bone graft substitute. When the procedure is performed at a young age, we recommend follow-up until skeletal maturity to identify recurrence of the deformity.
TYPE OF STUDY/LEVEL OF EVIDENCE: Therapeutic IV.
描述一系列采用纵行截骨术和植入骨替代物治疗先天性掌骨融合的病例。
我们回顾性分析了两家机构中所有接受纵行截骨术和植入骨替代物治疗的掌骨融合患者的病历。在初始诊断时、术中及末次随访时分析影像学和临床表现。
共有10例患者(14只手)符合纳入标准。6例患者(8只手)表现为环指与小指掌骨融合,4例患者(6只手)为中指与环指掌骨融合。手术时的中位年龄为5岁(范围2 - 16岁)。随访时间为1至14年(平均3年)。相关的手部畸形包括多指畸形、并指畸形和指骨弯曲畸形。术前,小指近节指骨平均向远离中指掌骨的方向成角46°(范围26° - 60°),中指与环指之间的成角平均为43°(范围26° - 50°)。对于环指与小指掌骨融合,术后1年的矫正角度具有统计学意义,平均为23°(范围10° - 30°);对于中指与环指掌骨融合,平均为16°(范围5° - 44°)。2例中指与环指掌骨融合的患者出现了手指外展复发。
掌骨融合是一种罕见的先天性手部畸形,其特征为相邻的两块掌骨融合。在最常见的形式中,环指和小指掌骨融合伴有小指处于外展位的异常姿势。所描述的技术使用安全有效,但对于轻度持续性成角和复发风险仍存在担忧。
先天性掌骨融合可通过纵行截骨术、调整掌骨排列并植入骨替代物进行有效治疗。当手术在幼年时进行,我们建议随访至骨骼成熟以发现畸形复发情况。
研究类型/证据水平:治疗性IV级。