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采用内骨段转移术矫正颅面骨比例失调引起的症状。

Internal distraction osteogenesis to correct symptomatic cephalocranial disproportion.

机构信息

Milwaukee, Wis. From the Department of Plastic Surgery, Craniofacial Center, Children's Hospital of Wisconsin, Medical College of Wisconsin.

出版信息

Plast Reconstr Surg. 2010 Nov;126(5):1677-1688. doi: 10.1097/PRS.0b013e3181ef8f65.

Abstract

BACKGROUND

Cephalocranial disproportion describes a state of volume mismatch between brain size and intracranial space. Nonsyndromic single-suture craniosynostosis patients can present with symptoms from elevated intracranial pressure because of inadequate or delayed treatment. The purpose of this study was to present five sagittal synostosis children with symptomatic cephalocranial disproportion treated with cranial vault distraction osteogenesis.

METHODS

Asymmetric transverse internal distraction osteogenesis was performed to preferentially expand the posterior cranium. A wider base plate, pivot screw, anterior hinge plate, and flexible drive rod were applied to minimize device failure while accomplishing lateral rotation of parietal bones. A distraction protocol was developed and produced consistent results.

RESULTS

Two girls and three boys underwent distraction for sagittal synostosis between 2002 and 2006. Average age at surgery was 5.8 years. All had resolution or amelioration of preoperative symptoms. Average operating room time for distractor placement was 2.5 hours (152 minutes) and average hospital stay was 2.8 days. The average distracted distance was 14.4 mm. Average operating room time for distractor removal was 1.1 hours (69 minutes) and average hospital stay was 1.6 days. No perioperative complications occurred. Average follow-up period was 4.2 years, with no recurrence of symptoms.

CONCLUSIONS

Symptomatic cephalocranial disproportion can present in older children with craniosynostosis. Asymmetric transverse distraction of the posterior cranial vault is a safe and effective treatment modality for this population.

摘要

背景

头盖颅比例失调描述的是大脑体积与颅内空间之间不匹配的状态。非综合征性单一颅缝早闭患者可能会因治疗不及时或不充分而出现颅内压升高的症状。本研究旨在介绍 5 例因颅缝早闭导致头盖颅比例失调而出现症状的矢状缝早闭患儿,他们接受了颅盖扩张成形术治疗。

方法

采用不对称横向内部分离骨成形术来优先扩张颅后窝。使用更宽的基底板、枢轴螺钉、前铰链板和柔性驱动杆,以最小化器械失效的风险,同时实现顶骨的侧向旋转。制定了一个牵引方案,取得了一致的效果。

结果

2002 年至 2006 年间,2 名女孩和 3 名男孩因矢状缝早闭接受了牵引治疗。手术时的平均年龄为 5.8 岁。所有患者的术前症状均得到缓解或改善。放置牵引器的平均手术室时间为 2.5 小时(152 分钟),平均住院时间为 2.8 天。平均牵引距离为 14.4 毫米。移除牵引器的平均手术室时间为 1.1 小时(69 分钟),平均住院时间为 1.6 天。无围手术期并发症发生。平均随访时间为 4.2 年,无症状复发。

结论

颅缝早闭的儿童可能会出现症状性头盖颅比例失调。对于这一人群,不对称的横向颅后窝牵引是一种安全有效的治疗方法。

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