继发于孤立性额蝶骨突畸形的前额畸形手术矫正术后的长期疗效:系统综述和两个说明性病例。

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY Child's Nervous System Pub Date : 2024-11-01 Epub Date: 2024-08-14 DOI:10.1007/s00381-024-06572-9
Felipe Gutierrez-Pineda, Juan Pablo Gutierrez Pineda, MMemet Özek
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引用次数: 0

摘要

目的:继发于孤立性额蝶骨突触(IFS)的前颅下垂(AP)是医学文献中记载的最罕见的颅骨突触症之一。因此,人们对这种小缝合畸形的术后长期(> 2 年)疗效缺乏全面了解:本研究介绍了两名曾接受过 IFS 治疗的患者的长期疗效,详细说明了他们的临床、影像学和术后特征。此外,本研究还按照 PRISMA 标准进行了系统性综述,总结了现有的相关文献。该综述特别关注 IFS 手术治疗后的长期美学效果、再手术率和并发症:系统性综述包括四篇文章,共涉及 12 名患者。综述重点介绍了临床特征、术后并发症、再次手术率和长期美容效果。手术平均年龄为 17.5 个月(9.5-24 个月),平均诊断年龄为 9.3 个月(6-10 个月)。眶前推进术是所有病例中最主要的手术方法。患者的再次手术率为16.6%,只有两例患者报告了术后并发症。在我们的一个病例中,术中 CT 扫描显示额骨对齐情况根据手术方案得到了实时改善,这对随访超过 24 个月的长期临床疗效起到了重要作用:IFS是一种罕见的轻微缝合突畸形,严重影响前额的美观,在处理AP病例时必须加以考虑。手术治疗的再手术率极低,长期预后良好。最近的机构数据和对当前文献的全面系统性回顾强化了这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Long-term outcomes after surgical correction of anterior plagiocephaly secondary to isolated frontosphenoidal synostosis: a systematic review and two illustrative cases.

Purpose: Anterior plagiocephaly ( AP), secondary to isolated frontosphenoidal synostosis (IFS), represents one of the rarest forms of craniosynostosis documented in medical literature. Therefore, there is a lack of comprehensive understanding regarding the long-term (> 2 years) postoperative outcomes of this minor suture synostosis.

Methods: This study presents the long-term outcomes of two patients previously treated for IFS, detailing their clinical, imaging, and postoperative characteristics. Additionally, a systematic review was conducted following PRISMA criteria to summarize existing literature on the topic. The review specifically focuses on long-term aesthetic outcomes, reoperation rates, and complications following surgical intervention for IFS.

Results: Four articles encompassing 12 patients were included in the systematic review. The review highlights clinical features, postoperative complications, reoperation rates, and long-term aesthetic outcomes. The mean age at surgery was 17.5 months (range 9.5-24 months), with an average age at diagnosis of 9.3 months (range 6-10 months). Fronto-orbital advancement was the predominant surgical approach described across all cases. The reoperation rate among patients was 16.6%, with only two cases reporting postoperative complications. In one of our cases, an intraoperative CT scan was utilized to illustrate real-time improvement in frontal bone alignment according to the surgical plan, which significantly contributed to positive long-term clinical outcomes observed during a follow-up period exceeding 24 months.

Conclusion: IFS, is a rare minor suture synostosis, significantly affects the aesthetic appearance of the forehead and necessitates consideration in the management of AP cases. Surgical intervention has shown minimal reoperation rates and excellent long-term prognosis. These findings are reinforced by recent institutional data and a comprehensive systematic review of the current literature.

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来源期刊
Child's Nervous System
Child's Nervous System 医学-临床神经学
CiteScore
3.00
自引率
7.10%
发文量
322
审稿时长
3 months
期刊介绍: The journal has been expanded to encompass all aspects of pediatric neurosciences concerning the developmental and acquired abnormalities of the nervous system and its coverings, functional disorders, epilepsy, spasticity, basic and clinical neuro-oncology, rehabilitation and trauma. Global pediatric neurosurgery is an additional field of interest that will be considered for publication in the journal.
期刊最新文献
Correction: Imaging features of pediatric meningiomas: emphasis on unusual locations. Correction: Occipital encephalocele: a retrospective analysis and assessment of post-surgical neurodevelopmental outcome. Radiographic severity is associated with worse executive function in metopic craniosynostosis. Occipital encephalocele: a retrospective analysis and assessment of post-surgical neurodevelopmental outcome. Vaulting further: cranial vault expansion for craniocerebral disproportion without primary craniosynostosis.
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