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足部多指畸形。文献综述与病例报告

Polydactyly of the foot. Literature review and case presentations.

作者信息

Galois L, Mainard D, Delagoutte J P

机构信息

Service de Chirurgie Orthopédique et Traumatologique (C.O.T), Hôpital Central, 29 avenue Maréchal de Lattre de Tassigny, C.O no. 34, 54035 Nancy, France.

出版信息

Acta Orthop Belg. 2002 Oct;68(4):376-80.

Abstract

Polydactyly is a fairly common congenital condition of the foot and is characterized literally by supernumerary toes (digit or metatarsal). The frequency of polydactyly varies widely among populations. It may be an isolated condition or part of a congenital syndrome. Polydactyly is generally classified into three major groups: medial ray (preaxial), central ray and lateral ray (postaxial). The duplication may appear at the distal and middle phalanges or at the whole digit and metatarsal. The complexity of the deformity ranges from a simple soft-tissue problem to a completely developed accessory ray. Careful clinical and radiographic evaluation should be made prior to treatment to achieve good functional and cosmetic results. Most cases are treated during childhood before walking age. Adult cases are more rare, and surgical management of the deformity is still debated. Nevertheless, surgery can be performed at any age as in our series with good results.

摘要

多指畸形是一种相当常见的足部先天性疾病,其字面特征是多趾(趾或跖骨)。多指畸形在不同人群中的发生率差异很大。它可能是一种孤立的病症,也可能是先天性综合征的一部分。多指畸形通常分为三大类:内侧射线(轴前型)、中央射线和外侧射线(轴后型)。多指可能出现在远端和中间指骨,也可能出现在整个趾和跖骨。畸形的复杂程度从简单的软组织问题到完全发育的副射线不等。治疗前应进行仔细的临床和影像学评估,以获得良好的功能和美容效果。大多数病例在儿童学步前接受治疗。成人病例较为罕见,畸形的手术治疗仍存在争议。然而,正如我们的系列病例所示,手术可在任何年龄进行,且效果良好。

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