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颅面短小畸形中的肋软骨移植术。

Costochondral grafting in craniofacial microsomia.

作者信息

Tahiri Youssef, Chang Catherine S, Tuin Jorien, Paliga J Thomas, Lowe Kristen M, Taylor Jesse A, Bartlett Scott P

机构信息

Indianapolis, Ind.; and Philadelphia, Pa. From the Division of Plastic Surgery, Indiana University, Riley Children's Hospital; and the Division of Plastic Surgery, Perelman School of Medicine at the University of Pennsylvania, The Children's Hospital of Philadelphia.

出版信息

Plast Reconstr Surg. 2015 Feb;135(2):530-541. doi: 10.1097/PRS.0000000000000914.

Abstract

BACKGROUND

Craniofacial microsomia encompasses a spectrum of diagnoses associated with variable degrees of mandibular hypoplasia, facial asymmetry, chin deviation, occlusal abnormalities, and potential airway compromise. This study presents one surgeon's experience with costochondral rib grafting for mandibular reconstruction in children with Pruzansky/Kaban type 2B and type 3 mandibular hypoplasia.

METHODS

An institutional review board-approved retrospective chart review was performed of all patients with craniofacial microsomia who underwent costochondral rib grafting for mandibular reconstruction performed by the senior author (S.P.B.) at The Children's Hospital of Philadelphia from January of 1998 to September of 2013. Demographic information, surgical history, operative details, postoperative complications, and outcomes were recorded. Plain radiographs and preoperative and postoperative three-dimensional computed tomographic scans were reviewed.

RESULTS

Two hundred fifty-five patients were diagnosed with craniofacial microsomia, and 22 patients met inclusion criteria. Twelve boys and 10 girls underwent grafting at an average age of 7.2 years. Thirty-three costochondral rib grafts were performed, 11 unilateral reconstructions and 11 bilateral reconstructions. Twelve hemimandibles were type 2B and 21 were type 3. No intraoperative complications were reported, and no incidence of graft resorption was noted. No additional procedures were required in 27 reconstructed hemimandibles (81.8 percent), whereas six (18.2 percent) required secondary distraction osteogenesis. Only one patient developed postoperative ankylosis. No malunion or nonunion was noted.

CONCLUSION

The approach described in this article allowed the authors to obtain reliably good results with costochondral rib grafting for type 2B and type 3 mandibular hypoplasia associated with craniofacial microsomia.

CLINICAL QUESTION/LEVEL OF EVIDENCE: Therapeutic, IV.

摘要

背景

颅面短小畸形包括一系列与不同程度下颌骨发育不全、面部不对称、颏部偏斜、咬合异常以及潜在气道受压相关的诊断。本研究介绍了一位外科医生使用肋软骨移植对普鲁赞斯基/卡班2B型和3型下颌骨发育不全患儿进行下颌骨重建的经验。

方法

对1998年1月至2013年9月在费城儿童医院由资深作者(S.P.B.)进行肋软骨移植下颌骨重建的所有颅面短小畸形患者进行了一项经机构审查委员会批准的回顾性病历审查。记录了人口统计学信息、手术史、手术细节、术后并发症和结果。回顾了X线平片以及术前和术后的三维计算机断层扫描。

结果

255例患者被诊断为颅面短小畸形,22例符合纳入标准。12名男孩和10名女孩接受了移植,平均年龄为7.2岁。共进行了33次肋软骨移植,其中11次为单侧重建,11次为双侧重建。12个半侧下颌骨为2B型,21个为3型。未报告术中并发症,也未发现移植吸收情况。27个重建的半侧下颌骨(81.8%)无需额外手术,而6个(18.2%)需要二期牵张成骨。仅1例患者出现术后关节强直。未发现骨不连或骨愈合不良。

结论

本文所述方法使作者能够通过肋软骨移植对与颅面短小畸形相关的2B型和3型下颌骨发育不全可靠地获得良好效果。

临床问题/证据级别:治疗性,IV级。

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