Belthur Mohan Venkatnarsimha, Linton Judith Lynn, Barnes Douglas Agna
Pediatric Orthopedic Service, Shriners Hospitals for Children, Houston, TX 77030, USA.
J Pediatr Orthop. 2011 Jun;31(4):435-47. doi: 10.1097/BPO.0b013e3182199a68.
Polydactyly is a common congenital anomaly of the foot classified as preaxial, central, or postaxial depending on the location of the duplication. Approximately 15% of all duplications of the toes are preaxial. The purpose of this study is to report our experience in the management of preaxial polydactyly of the foot over a period of 30 years at a single institution.
This is a retrospective institutional review board-approved descriptive case series of 21 children representing 28 feet with preaxial foot polydactyly seen at our institution from 1977 to 2009. All subjects were analyzed in terms of sex, laterality, anatomic patterns of polydactyly, associated anomalies, family history, clinical features, surgical indications, details of surgical procedures, and outcomes after surgical interventions, using data collected from medical records, radiographs, and clinical photographs. Clinical outcomes were evaluated at the most recent examination, according to the format published by Phelps and Grogan.
There were 21 patients (28 feet) including 11 male and 10 female subjects. Duplications were bilateral in 7 patients and unilateral in 14. The average age at surgery was 1.8 years (range: 0.8 to 4.6 y). The average follow-up was 81.7 months (range: 5 to 180 mo). According to the Watanabey classification, the distal phalangeal type occurred in 4 feet, the proximal phalangeal type in 10 feet, the metatarsal type in 10 feet, the tarsal type in 2 feet, a combined tarsal and metatarsal type in 1 foot, and a mirror type in 1 foot. All patients had associated anomalies in the affected feet. Congenital hallux varus was the most common associated anomaly (20 feet). A longitudinal epiphyseal bracket was observed in 4 feet. Clinical outcomes after the initial surgery were excellent in 8 feet, good in 15 feet, and poor in 5 feet. The 5 feet rated as poor were because of residual deformities and required additional surgery. Good results were subsequently obtained at final follow-up in all 5 feet.
In our opinion, the Watanabe classification is more useful than the Venn-Watson for surgical planning. However, we have added an additional type, representing a mirror foot which we feel is within the overall spectrum of preaxial polydactyly. Good or better results were obtained in all feet at final follow-up. Early detection and adequate excision of the longitudinal bracket affecting the phalanges or metatarsal can reduce residual deformity and the need for revision surgery.
多指畸形是一种常见的足部先天性异常,根据重复部位的不同可分为轴前型、中央型或轴后型。所有脚趾重复畸形中约15%为轴前型。本研究的目的是报告我们在一家机构30年间对足部轴前型多指畸形的治疗经验。
这是一项经机构审查委员会批准的回顾性描述性病例系列研究,纳入了1977年至2009年在我们机构就诊的21例患有轴前型足部多指畸形的儿童,共28只脚。利用从病历、X光片和临床照片中收集的数据,对所有受试者的性别、左右侧、多指畸形的解剖模式、相关异常、家族史、临床特征、手术指征、手术细节以及手术干预后的结果进行了分析。根据费尔普斯和格罗根发表的格式,在最近一次检查时评估临床结果。
共有21例患者(28只脚),其中男性11例,女性10例。7例患者为双侧重复畸形,14例为单侧。手术时的平均年龄为1.8岁(范围:0.8至4.6岁)。平均随访时间为81.7个月(范围:5至180个月)。根据渡边分类法,远端指骨型4只脚,近端指骨型10只脚,跖骨型10只脚,跗骨型2只脚,跗骨和跖骨联合型1只脚,镜像型1只脚。所有患者患侧足部均有相关异常。先天性拇内翻是最常见的相关异常(20只脚)。4只脚观察到纵向骨骺支架。初次手术后的临床结果为:优8只脚,良15只脚,差5只脚。评为差的5只脚是因为残留畸形,需要再次手术。在最终随访时,所有5只脚均取得了良好的结果。
我们认为,渡边分类法在手术规划方面比维恩 - 沃森分类法更有用。然而,我们增加了一种额外的类型,即镜像足,我们认为它属于轴前型多指畸形的总体范畴。在最终随访时,所有足部均取得了良好或更好的结果。早期发现并充分切除影响指骨或跖骨的纵向支架可减少残留畸形和再次手术的必要性。