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Ⅱ型腓骨半侧发育不全患儿骨延长术后胫骨和踝关节畸形复发的预防

Prevention of recurrence of tibia and ankle deformities after bone lengthening in children with type II fibular hemimelia.

作者信息

Popkov Arnold, Aranovich Anna, Popkov Dmitry

机构信息

Russian Ilizarov Scientific Centre for Restorative Traumatology and Orthopaedics, 6, M.Ulyanova street, 640014, Kurgan, Russian Federation.

出版信息

Int Orthop. 2015 Jul;39(7):1365-70. doi: 10.1007/s00264-015-2752-4. Epub 2015 Apr 2.

DOI:10.1007/s00264-015-2752-4
PMID:25832175
Abstract

PURPOSE

This study aimed to evaluate development of the tibia after Ilizarov lengthening and deformity correction depending on whether or not the simultaneous resection of fibular anlage was performed in children with fibular aplasia type II, who did not undergo early surgery.

METHODS

The study analyses results of reconstructive treatment in 38 children at the age of over four years. Two groups of children are compared: bifocal tibial lengthening with the Ilizarov device (group I) and bifocal lengthening associated with resection of the fibular anlage (group II). The results were estimated at 12 months and in the long-term exceeding three years.

RESULTS

Radiological data of measurement of the anatomical lateral distal tibial angle (aLDTA) show surgical correction of deformities achieved in both groups. During the further limb growth a tendency to normalisation of the aLDTA was observed only in the group II. Quick relapse of the angular deformities of the tibial shaft in the first group occurred mainly during further growth of the limb regardless of complete correction at the time of treatment. On the other hand, there were no recurrences of diaphyseal deformities in the group II.

CONCLUSIONS

In children with congenital fibular deficiency of type II at the age of four years, the bone lengthening and deformity correction should be associated with fibular anlage resection. That approach improves conditions for distal tibia development and prevents or decreases significantly the recurrence of deformities of the tibia and ankle joint in long-term follow-up.

摘要

目的

本研究旨在评估II型腓骨发育不全且未接受早期手术的儿童在Ilizarov延长及畸形矫正术后胫骨的发育情况,具体取决于是否同时切除腓骨原基。

方法

本研究分析了38名4岁以上儿童的重建治疗结果。比较了两组儿童:使用Ilizarov器械进行双焦点胫骨延长术的儿童(第一组)和与腓骨原基切除术相关的双焦点延长术的儿童(第二组)。在12个月时以及超过3年的长期随访中评估结果。

结果

测量胫骨远端外侧解剖角(aLDTA)的放射学数据显示两组均实现了畸形的手术矫正。在肢体进一步生长过程中,仅在第二组中观察到aLDTA有趋于正常化的趋势。第一组胫骨干角畸形的快速复发主要发生在肢体进一步生长期间,尽管在治疗时已完全矫正。另一方面,第二组中骨干畸形没有复发。

结论

对于4岁的II型先天性腓骨缺如儿童,骨延长和畸形矫正应与腓骨原基切除术相结合。这种方法改善了胫骨远端发育的条件,并在长期随访中预防或显著减少了胫骨和踝关节畸形的复发。

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