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颅缝早闭的治疗

Management of craniosynostosis.

作者信息

Panchal Jayesh, Uttchin Venus

机构信息

Oklahoma University Health Science Center, Oklahoma 73104, USA.

出版信息

Plast Reconstr Surg. 2003 May;111(6):2032-48; quiz 2049. doi: 10.1097/01.PRS.0000056839.94034.47.

Abstract

After studying this article, the participant should be able to: 1. Review the etiopathogenesis of craniosynostosis and craniofacial anomalies. 2. Develop a basic understanding of the clinical manifestations and diagnosis of craniofacial anomalies. 3. Describe the surgical principles of managing craniosynostosis and craniofacial anomalies.Craniosynostosis, or the premature closure of calvarial sutures, results in deformed calvaria at birth. Although the etiology of craniosynostosis is currently unknown, animal experiments and a recent interest in molecular biology point toward interplay between the dura and the underlying brain. This interaction occurs by means of a local alteration in the expression of transforming growth factor, MSX2, fibroblast growth factor receptor, and TWIST. The fused suture restricts growth of the calvaria, thus leading to a characteristic deformation, each associated with a different type of craniosynostosis. Uncorrected craniosynostosis leads to a continuing progression of the deformity, and in some cases, an elevation of intracranial pressure. Clinical examination should include not only an examination of the skull but also a general examination to rule out the craniofacial syndromes that accompany craniosynostosis. Because deformational plagiocephaly, or plagiocephaly without synostosis, occurs secondary to sleeping in the supine position during the early perinatal period, the physician should be aware of this abnormality. Treatment for deformational plagiocephaly is conservative when compared with treatment for craniosynostosis, which requires surgery. Appropriate investigations should include genetic screening, radiologic examination with a computerized tomographic scan, and neurodevelopmental analysis. Surgical intervention should be performed during infancy, preferably in the first 6 months of postnatal life, to prevent the further progression of the deformity and possible complications associated with increased intracranial pressure. The principles of surgical intervention are not only to excise the fused suture but also to attempt to normalize the calvarial shape. Long-term follow-up is critical to determine the effect of the surgical outcome.

摘要

学习本文后,读者应能够:1. 回顾颅缝早闭和颅面畸形的病因发病机制。2. 对颅面畸形的临床表现和诊断形成基本认识。3. 描述治疗颅缝早闭和颅面畸形的手术原则。颅缝早闭,即颅骨缝过早闭合,会导致出生时颅骨变形。虽然颅缝早闭的病因目前尚不清楚,但动物实验以及近期对分子生物学的关注表明硬脑膜与下方大脑之间存在相互作用。这种相互作用通过转化生长因子、MSX2、成纤维细胞生长因子受体和TWIST表达的局部改变而发生。融合的颅骨缝会限制颅骨生长,从而导致特征性变形,每种变形与不同类型的颅缝早闭相关。未经矫正的颅缝早闭会导致畸形持续进展,在某些情况下还会导致颅内压升高。临床检查不仅应包括对头骨的检查,还应进行全面检查以排除伴随颅缝早闭的颅面综合征。由于变形性斜头畸形,即无颅骨缝早闭的斜头畸形,继发于围产期早期仰卧位睡眠,医生应了解这种异常情况。与需要手术治疗的颅缝早闭相比,变形性斜头畸形的治疗较为保守。适当的检查应包括基因筛查、计算机断层扫描的放射学检查以及神经发育分析。手术干预应在婴儿期进行,最好在出生后的头6个月内,以防止畸形进一步发展以及与颅内压升高相关的可能并发症。手术干预的原则不仅是切除融合的颅骨缝,还应尝试使颅骨形状正常化。长期随访对于确定手术效果至关重要。

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