Mid-Term Follow-Up Results of Surgical Reconstruction for Congenital Hallux Varus with Polysyndactyly in Children.

IF 0.6 4区 医学 Q4 ORTHOPEDICS
Boyan Boyanov Hristov, Sofia Valentinova Nikolova, Alexandar Ivanov Gerchev, Stefan Stefanov Tserovski, Hristo Dimitrov Georgiev
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引用次数: 0

Abstract

Purpose of the study: Congenital hallux varus associated with preaxial polysyndactyly of the foot is a rare deformity for which standardized treatment protocols and outcome data remain limited. The purpose of this study was to evaluate the mid-term clinical and radiographic outcomes of early surgical reconstruction in a consecutive pediatric series.

Material and methods: Between 2015 and 2023, eight affected feet in seven children with congenital preaxial polysyndactyly and hallux varus were surgically treated at a single tertiary pediatric orthopedic center. The diagnosis was established at birth. The mean age at surgery was 31.62 ± 36.64 months. All patients exhibited varus deviation of the first ray, duplication of the distal phalanx, complete or partial duplication of the proximal phalanx, soft-tissue syndactyly, duplicated or shared nail plates, and a hypoplastic medial ray. Surgical treatment consisted of resection of the hypoplastic medial hallux, abductor hallucis tenotomy, excision of chondrofibrous bands when present, subtotal periosteal stripping of the first metatarsal, and medial open-wedge osteotomy of the first metatarsal or proximal phalanx in selected cases. Outcomes were assessed clinically and radiographically, and graded using the Phelps and Grogan classification.

Results: At a mean follow-up of 45.14 ± 18.79 months (range, 24 to 82 months), satisfactory outcomes were achieved in 87.5% of the treated feet. Significant correction of the hallux varus deformity was obtained, with preservation of motion of the first metatarsophalangeal and interphalangeal joints. No patient required secondary surgical procedures. One patient who did not undergo initial metatarsal osteotomy demonstrated progressive recurrent varus during follow-up.

Conclusions: Early surgical correction of congenital hallux varus polysyndactyly (between 12 and 18 months of age) yields favorable mid-term outcomes. Medial open-wedge osteotomy of the first metatarsal represents a critical component for durable correction and should be considered even in low-grade deformities.

小儿先天性拇内翻合并多趾畸形手术重建术中期随访结果。
研究目的:先天性拇内翻合并足前轴多指畸形是一种罕见的畸形,标准化的治疗方案和结果数据仍然有限。本研究的目的是在连续的儿科系列中评估早期手术重建的中期临床和影像学结果。材料和方法:2015年至2023年,在一家三级儿科骨科中心对7例先天性轴前多指拇内翻患儿中的8例患足进行手术治疗。诊断是在出生时确定的。平均手术年龄为31.62±36.64个月。所有患者均表现为首线内翻偏,远端指骨重复,近端指骨完全或部分重复,软组织并指,甲板重复或共用,内侧线发育不全。手术治疗包括切除发育不全的内侧拇趾,外展拇腱切断术,存在软骨纤维带切除,第一跖骨近全骨膜剥离,以及在选定的病例中对第一跖骨或近端指骨进行内侧楔形开骨切断术。临床和影像学评估结果,并使用Phelps和Grogan分级进行分级。结果:平均随访45.14±18.79个月(24 ~ 82个月),87.5%的治疗足获得满意结果。拇内翻畸形得到了显著的矫正,保留了第一跖趾和指间关节的运动。没有患者需要二次手术。一名未接受初始跖骨截骨术的患者在随访期间表现出进行性复发性内翻。结论:早期手术矫正先天性多并指拇内翻(12 - 18个月大)中期预后良好。第一跖骨内侧开楔截骨是持久矫正的关键组成部分,即使是轻度畸形也应考虑。
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来源期刊
CiteScore
0.70
自引率
25.00%
发文量
53
期刊介绍: Editorial Board accepts for publication articles, reports from congresses, fellowships, book reviews, reports concerning activities of orthopaedic and other relating specialised societies, reports on anniversaries of outstanding personalities in orthopaedics and announcements of congresses and symposia being prepared. Articles include original papers, case reports and current concepts reviews and recently also instructional lectures.
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