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三叶草颅骨畸形行后颅窝减压术后的继发性额缝早闭

Secondary metopic craniosynostosis after posterior cranial decompression in cloverleaf skull deformity.

作者信息

Chaisrisawadisuk Sarut, Khampalikit Inthira, Chankaew Ekawut, Moore Mark H

机构信息

Division of Plastic Surgery, Department of Surgery, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

Cleft and Craniofacial South Australia, Women's and Children's Hospital, North Adelaide, SA, Australia.

出版信息

Childs Nerv Syst. 2024 Jun;40(6):1937-1941. doi: 10.1007/s00381-024-06309-8. Epub 2024 Feb 7.

DOI:10.1007/s00381-024-06309-8
PMID:38324062
Abstract

Cloverleaf skull deformity or Kleeblattschadel syndrome is a severe condition where multiple cranial sutures are absent and prematurely fused, leading to a trilobate head shape. The remaining open sutures or fontanelles compensate for rapid brain expansion, while the constricted fused calvarium restricts brain growth and results in increased intracranial pressure. Recent data show that early posterior cranial and foramen magnum decompression positively affects infants with cloverleaf skulls. However, long-term sequelae are still rarely discussed. We hereby report a child who developed secondary metopic craniosynostosis after posterior cranial decompression, which required a front-orbital advancement and cranial remodelling as a definitive procedure.

摘要

三叶草颅骨畸形或 Kleeblattschadel 综合征是一种严重的病症,表现为多条颅缝缺失且过早融合,导致头部呈三叶形。剩余开放的颅缝或囟门可补偿大脑的快速扩张,而狭窄融合的颅骨则限制大脑生长并导致颅内压升高。近期数据表明,早期进行后颅窝和枕骨大孔减压对患有三叶草颅骨畸形的婴儿有积极影响。然而,长期后遗症仍很少被讨论。我们在此报告一名儿童,其在进行后颅窝减压后出现了继发性额缝早闭,这需要进行额眶前移和颅骨重塑作为确定性手术。

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Childs Nerv Syst. 2024 Jun;40(6):1937-1941. doi: 10.1007/s00381-024-06309-8. Epub 2024 Feb 7.
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本文引用的文献

1
Re-imagining early cloverleaf skull deformity management from front to back approach-30 years on.从前到后重新构想早期三叶草颅骨畸形的管理方法——30 年后的思考。
Childs Nerv Syst. 2023 Dec;39(12):3349-3359. doi: 10.1007/s00381-023-06147-0. Epub 2023 Sep 12.
2
Mechanical loading of cranial joints minimizes the craniofacial phenotype in Crouzon syndrome.颅骨关节的机械加载可最大限度地减少颅面型在克劳宗综合征中的表现。
Sci Rep. 2022 Jun 11;12(1):9693. doi: 10.1038/s41598-022-13807-9.
3
Posterior Vault Distraction Outcomes in Patients With Severe Crouzon Syndrome Resulting from Ser347Cys and Ser354Cys Mutations.
S347C 和 S354C 突变导致的严重颅缝早闭综合征患者颅顶后区牵张的结果。
J Craniofac Surg. 2022;33(5):1545-1548. doi: 10.1097/SCS.0000000000008642. Epub 2022 Mar 10.
4
Secondary Coronal Synostosis After Early Surgery for Sagittal Craniosynostosis: Implications for Cranial Growth.矢状缝早切术后继发冠状缝融合:对颅缝生长的影响。
J Craniofac Surg. 2021;32(1):113-117. doi: 10.1097/SCS.0000000000007087.
5
Severe Cloverleaf Skull Deformity in c.1061C>G (p.Ser354Cys) Mutated Fibroblast Growth Factor Receptor 2 Gene in Crouzon Syndrome.Crouzon 综合征中纤维母细胞生长因子受体 2 基因 c.1061C>G(p.Ser354Cys)突变导致严重的三叶形颅面骨畸形。
J Craniofac Surg. 2021;32(1):261-264. doi: 10.1097/SCS.0000000000006999.
6
Secondary Suture Fusion after Primary Correction of Nonsyndromic Craniosynostosis: Recognition of the Problem and Identification of Risk Factors.非综合征性颅缝早闭初次矫正术后的二次缝合融合:问题的认识和危险因素的确定。
Plast Reconstr Surg. 2020 Feb;145(2):493-503. doi: 10.1097/PRS.0000000000006491.
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Physiologic closure time of the metopic suture in South Australian infants from 3D CT scans.通过三维CT扫描确定南澳大利亚婴儿额缝的生理性闭合时间。
Childs Nerv Syst. 2019 Feb;35(2):329-335. doi: 10.1007/s00381-018-3957-9. Epub 2018 Sep 14.
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Determining the fate of cranial sutures after surgical correction of non-syndromic craniosynostosis.确定非综合征性颅缝早闭术后颅缝命运。
J Craniomaxillofac Surg. 2017 Nov;45(11):1801-1808. doi: 10.1016/j.jcms.2017.08.009. Epub 2017 Aug 19.
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New-onset craniosynostosis after posterior vault distraction osteogenesis.后颅穹窿牵张成骨术后新发颅骨缝早闭
J Craniofac Surg. 2015 Jan;26(1):176-9. doi: 10.1097/SCS.0000000000001186.
10
Pathology in metopic synostosis.冠状缝早闭的病理学
Childs Nerv Syst. 2013 Dec;29(12):2165-70. doi: 10.1007/s00381-013-2284-4. Epub 2013 Oct 3.