Fearon Jeffrey A
Craniofacial Center, North Texas Hospital for Children, Medical City Dallas, USA.
Plast Reconstr Surg. 2003 Jul;112(1):1-12; discussion 13-9. doi: 10.1097/01.PRS.0000065908.60382.17.
Apert syndrome is a relatively uncommon condition that is instantly recognizable on the basis of the pan-syndactylies involving both the hands and feet. For more than 10 years, the treatment of Apert syndrome hand and foot anomalies was approached in a comprehensive manner, with attempts to maximize the final results and minimize the total number of operations. Numerous conventions were abandoned in the development of this approach, with the introduction of some new methodologies, including (1) release of all 10 fingers, and toes, in only two operations, (2) elimination of routine digital amputations, (3) abandonment of the zigzag incision in favor of straight-line release, (4) substitution of equal-length anterior and posterior flaps for the long dorsal web space lining flap, (5) leaving of small areas of exposed bone without vascularized tissue coverage, and (6) performance of midphalangeal osteotomies, among older children, to improve hand function. Fifty-seven children with Apert syndrome have been treated at the author's center since 1990, and 43 underwent surgical treatment of their hands and feet by a single surgeon. Treatment can be separated into two phases, early (syndactyly releases) and late (functional osteotomies). Seventeen of those 43 patients were treated at the author's center from birth (type I, 11 patients; type II, two patients; type III, four patients), and 10 fingers and 10 toes were achieved for all patients in two operations. No digital amputations were performed for any of the 43 patients. However, four of 26 patients (15 percent) not treated at the author's center from birth had undergone at least one digital amputation before coming to the center. Twenty-two of those 26 patients required a two-stage syndactyly release to accomplish the separation of all 10 fingers and toes. Aside from the patients who had previously undergone amputations, all other patients successfully achieved 10 fingers and toes, except for one patient (38 of 39 patients, 97 percent). The average operative time for the first-stage syndactyly release of the hands and feet was 4 hours 11 minutes (range, 185 to 300 minutes), and that for the second stage was 3 hours 49 minutes (range, 160 to 300 minutes). Twenty-eight hands were treated with functional osteotomies, which involved permanent angulation of the fused phalanges at the proximal interphalangeal level, to create a "position of function" and provide pulp-to-pulp pinch. In addition, targeted osteotomies of the feet were performed for many of these patients, to decrease pain with walking. There were no major complications. Minor complications included one reexploration because of bleeding, early in the series. There were 13 incomplete secondary syndactylies that required a subsequent operative release (10 spaces treated at the author's center and three treated elsewhere), of a total of 342 spaces (3 percent author incidence). There were no scar contractures or functional limitations that required release. This distinctive protocol seemed to result in improved functional outcomes, with a reduction in the total number of operative procedures.
Apert综合征是一种相对罕见的疾病,基于累及双手和双足的全并指(趾)畸形,很容易识别。十多年来,Apert综合征手足畸形的治疗采用综合方法,试图使最终结果最大化,并尽量减少手术总数。在这种方法的发展过程中,摒弃了许多传统做法,引入了一些新方法,包括:(1)仅通过两次手术就松解全部10个手指和脚趾;(2)取消常规的手指截肢;(3)放弃锯齿状切口,改用直线松解;(4)用等长的前后皮瓣替代长的背侧蹼间隙衬里皮瓣;(5)留下小面积无血管化组织覆盖的暴露骨;(6)对大龄儿童进行中节指骨截骨术,以改善手部功能。自1990年以来,作者所在中心共治疗了57例Apert综合征患儿,其中43例由同一外科医生进行了手足手术治疗。治疗可分为两个阶段,早期(并指松解)和晚期(功能性截骨术)。这43例患者中有17例自出生起就在作者所在中心接受治疗(I型11例,II型2例,III型4例),所有患者均通过两次手术获得了10个手指和10个脚趾。43例患者均未进行手指截肢。然而,26例非自出生起就在作者所在中心接受治疗的患者中,有4例(15%)在来该中心之前至少接受过一次手指截肢。这26例患者中有22例需要分两期进行并指松解,以实现全部10个手指和脚趾的分离。除了之前接受过截肢的患者外,所有其他患者均成功获得了10个手指和脚趾,只有1例除外(39例患者中的38例,97%)。手足一期并指松解的平均手术时间为4小时11分钟(范围为185至300分钟),二期为3小时49分钟(范围为160至300分钟)。28只手接受了功能性截骨术,即在近端指间关节水平对融合的指骨进行永久性成角,以形成“功能位”并实现指尖对指尖捏取。此外,对其中许多患者的足部进行了针对性截骨术,以减轻行走时的疼痛。无重大并发症。轻微并发症包括该系列早期有1例因出血而再次手术探查。共有13处不完全性继发性并指需要后续手术松解(作者所在中心治疗10处间隙,其他地方治疗3处间隙),总共342处间隙(作者所在中心发生率为3%)。无需要松解的瘢痕挛缩或功能受限情况。这种独特的方案似乎能改善功能结果,并减少手术总数。