并发颅畸形和位置性长颅畸形:范围审查

FACE Pub Date : 2024-05-11 DOI:10.1177/27325016241252953
Gwendolyn E. Daly, Peter Ferrin, J. Carboy, Lori K. Howell, Nathan R Selden, Erik M. Wolfswinkel
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引用次数: 0

摘要

颅骨发育不全(Craniosynostosis)和位置性头盖骨畸形(PP)都会导致婴儿颅骨畸形。在某些情况下,患者可能会同时出现颅骨发育不良和位置性颅骨发育不良。这两种疾病对颅骨的作用力会使正确诊断变得复杂和延迟,并需要调整手术计划。本次范围界定综述旨在识别和分析现有的同行评议文献,这些文献涉及并发颅骨发育不良和 PP 的诊断和治疗。根据 PRISMA 指南,我们在 PubMed、MEDLINE 和 EMBASE 上检索了讨论并发颅骨发育不良和 PP 诊断的文章。在发现的 633 篇文章中,有 7 篇符合纳入标准,累计讨论了 10 名患者。转诊到颅颌面团队的平均年龄为(17 ± 22.2)个月。最常见的转诊原因是颅面不对称(90%,n = 9)。40%为单侧冠状突畸形(4例),40%为羊角突畸形(4例),10%为矢状突畸形(1例),10%为偏侧突畸形(1例)。最常见的临床特征是枕骨变平(90%,9 例)、耳朵移位(80%,8 例)和额部隆起(30%,3 例)。70%(7 例)患者的初步诊断延迟或不正确。CT 扫描是最常用的诊断工具,100% 的患者都进行了 CT 扫描。70%的患者(7 例)在平均年龄(6.75 ± 3 个月)时接受了手术。有两项研究(占报告患者总数的 2%)指出,除了合体缝合外,他们还改变了手术技术以考虑 PP。并发颅骨发育不良和 PP 可带来复杂的诊断和治疗难题。深入了解与每种颅合畸形合并 PP 相关的最可靠的体格检查结果将有助于准确诊断。考虑到颅骨失稳和 PP 同时对颅骨产生的作用力,有助于设计量身定制的手术方案。
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Concurrent Craniosynostosis and Positional Plagiocephaly: A Scoping Review
Craniosynostosis and positional plagiocephaly (PP) both lead to deformities of the infant skull. In some cases, patients may present with concurrent craniosynostosis and PP. The forces exerted on the skull by both conditions can complicate and delay correct diagnosis and require adjustments to surgical planning. The purpose of this scoping review was to identify and analyze the existing peer-reviewed literature covering the diagnosis and treatment of concurrent craniosynostosis and PP. In accordance with PRISMA guidelines, PubMed, MEDLINE, and EMBASE were searched for articles discussing concurrent diagnoses of craniosynostosis and PP. Out of 633 articles discovered, 7 met inclusion criteria and discussed a cumulative total of 10 patients. The average age of referral to a craniofacial team was 17 ± 22.2 months. The most common reason for referral was craniofacial asymmetry (90%, n = 9). 40% presented with unilateral coronal synostosis (n = 4), 40% with lambdoid synostosis (n = 4), 10% with sagittal synostosis (n = 1), and 10% with metopic synostosis (n = 1). The most commonly reported clinical features were occipital flattening (90%, n = 9), ear displacement (80%, n = 8), and frontal bossing (30%, n = 3). Delayed or incorrect initial diagnosis was noted in 70% (n = 7) of patients. CT scan was the most commonly employed diagnostic tool, utilized in 100% of patients. 70% of patients (n = 7) underwent surgery at an average age of 6.75 ± 3 months. Two studies, accounting for 2 patients reported, noted altering their surgical technique to account for PP in addition to the synostotic suture. Coincident craniosynostosis and PP can pose a complicated diagnostic and therapeutic challenge. An in-depth understanding of the most reliable physical exam findings associated with each type of craniosynostosis combined with PP will facilitate accurate diagnosis. Consideration of the concurrent forces on the skull created by craniosynostosis and PP aid in the design of a tailored surgical plan.
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