Hand Surgery and Microsurgery Department, Azienda Ospedaliero Universitaria Integrata di Verona, Italy.
Hand Surgery and Microsurgery Department, Azienda Ospedaliero Universitaria di Modena, Italy.
J Hand Surg Asian Pac Vol. 2022 Apr;27(2):233-241. doi: 10.1142/S2424835522500308. Epub 2022 Mar 31.
Clinical manifestations of camptodactyly are varied and no official consensus on the etiopathogenesis or best treatment is available. Conservative treatment is generally preferred and, in refractory patients, surgery might be considered. However, reported results of surgery are often unsatisfactory and it is difficult to compare outcomes as different classification systems are adopted. We reported the outcomes of surgical treatment of camptodactyly with the Malek cutaneous approach and stepwise release, assessed using the Siegert classification. A retrospective analysis of paediatric patients (≥1 and ≤18 years) with congenital camptodactyly refractory to conservative management (flexion contracture >30°), treated with Malek cutaneous approach and stepwise release surgery between June 2009 and June 2019 with at least 1 year of follow-up was performed. Pre- and post-operative clinical and radiographic assessments were evaluated for degrees of flexion contractures and early (<30 days) or late (>30 days) complications were recorded. A total of 59 patients underwent surgery, of whom 38 (64%), including 42 fingers, were enrolled; mean patient age was 8 years (range 1-18). Post-operative mean flexion contracture was significantly improved ( > 0.001) and no infections were recorded. Mean follow-up was 6 years (range 1-10) and proximal interphalangeal joint extension deficits were rated according to Siegert classification as excellent (69%), good (12%), or fair (9.5%) and poor (9.5%). The Malek cutaneous approach and stepwise release of the retracting soft tissues allow prompt evaluation of the anatomical structures involved in the deformity and seem to be an effective surgical correction in the long term. Level IV (Therapeutic).
先天性掌指屈肌腱挛缩畸形的临床表现多种多样,其病因及最佳治疗方法尚无明确共识。一般倾向于保守治疗,对于难治性患者可考虑手术。然而,手术的报道结果往往不尽人意,由于采用了不同的分类系统,很难比较结果。我们报告了采用 Malek 皮下游离加逐步松解术治疗先天性掌指屈肌腱挛缩畸形的结果,采用 Siegert 分类进行评估。
对 2009 年 6 月至 2019 年 6 月间采用 Malek 皮下游离加逐步松解术治疗的 59 例(38 指)难治性先天性掌指屈肌腱挛缩畸形(弯曲挛缩>30°)且至少随访 1 年的儿童患者(年龄 1-18 岁)进行回顾性分析。评估术前和术后的临床和影像学评估弯曲挛缩程度,并记录早期(<30 天)和晚期(>30 天)并发症。
所有患者均行手术治疗,其中 38 例(64%),包括 42 指纳入研究;患者平均年龄 8 岁(1-18 岁)。术后平均弯曲挛缩显著改善(>0.001),无感染记录。平均随访 6 年(1-10 年),根据 Siegert 分类,近节指间关节伸展不足评定为优(69%)、良(12%)、可(9.5%)和差(9.5%)。
Malek 皮下游离加逐步松解挛缩的软组织可快速评估畸形涉及的解剖结构,似乎是一种有效的长期手术矫正方法。
Ⅳ级(治疗)。