Poul J, Veselý J, Gál P, Bajerová J, Justan I
Klinika Detské Chirurgie, Ortopedie a Traumatologie FN, Brno.
Acta Chir Orthop Traumatol Cech. 2006;73(1):10-7.
The aim of the study was to evaluate the results in a group of patients with congenital pseudarthrosis of the tibia treated by transfer of a vascularized fibular graft from the contralateral extremity.
The group included three boys and two girls aged 2 to 8 years at the time of surgery. In two patients, the vascularized graft transfer was preceded by other operations. All patients but one had Crawford type IV pseudarthrosis. The signs of peripheral neurofibromatosis were found in four of the five patients.
The operation was carried out by two surgical teams, i. e., orthopedic and microsurgery (plastic surgery) specialists. Deep dissection of the pseudarthrosis was performed down to healthy, well vascularized tissue; a vascularized pedicle bone graft was harvested from the contralateral fibula. The graft was inserted and anchored intramedullarily in both tibial fragments, and stability was provided with a K-wire introduced through the calcaneus. Subsequently, the vascular pedicle of the fibular graft was joined to the surrounding vessels (anterior tibial artery and anterior tibial vein). The extremity was immobilized in plaster cast and later a KAFO brace was applied.
Graft union partially failed in the proximal end of the graft due to bone resorption of both the graft and the proximal tibial fragment in two patients. This was successfully treated by additional spongioplasty. In all patients bony union was achieved at an average time of 9.8 months (range, 6 to 21 months). An increase by more than 100 % in the diameter of the transplanted fibula was recorded in four patients. The increase, which was of course related to follow-up time, was a clear proof of primary graft vascularization.
The use of vascularized fibular graft harvested from the contralateral extremity showed high effectiveness in comparison with other methods. This was in agreement with the relevant literature reports.
This method can be used regardless of patients' age and our experience showed that, even in small children, union can be achieved and can thus allow for early weight-bearing and prevention of crus atrophy.
本研究旨在评估一组采用对侧带血管腓骨移植治疗的先天性胫骨假关节患者的治疗效果。
该组包括3名男孩和2名女孩,手术时年龄为2至8岁。2例患者在带血管移植之前接受过其他手术。除1例外,所有患者均为克劳福德IV型假关节。5例患者中有4例发现有周围神经纤维瘤病体征。
手术由两个手术团队进行,即骨科和显微外科(整形外科)专家。对假关节进行深入解剖,直至健康、血运良好的组织;从对侧腓骨获取带血管蒂骨移植。将移植骨插入并髓内固定于胫骨的两个断端,通过跟骨插入克氏针以提供稳定性。随后,将腓骨移植的血管蒂与周围血管(胫前动脉和胫前静脉)吻合。肢体用石膏固定,之后应用膝踝足矫形器。
2例患者由于移植骨和胫骨近端骨块的骨吸收,移植骨近端部分愈合失败。通过额外的骨松质成形术成功治疗。所有患者平均在9.8个月(范围6至21个月)实现骨愈合。4例患者记录到移植腓骨直径增加超过100%。这种增加当然与随访时间有关,是移植骨最初血管化的明确证据。
与其他方法相比,采用对侧带血管腓骨移植显示出高效性。这与相关文献报道一致。
该方法可用于任何年龄的患者,我们的经验表明,即使是幼儿也能实现愈合,从而可早期负重并预防小腿萎缩。