The role of the posterior fossa in developing Chiari I malformation in children with craniosynostosis syndromes

被引:26
作者
Rijken, Bianca Francisca Maria [1 ]
Lequin, Maarten Hans [2 ]
van der Lijn, Fedde [3 ,4 ]
van Veelen-Vincent, Marie-Lise Charlotte [5 ]
de Rooi, Johan [6 ]
Hoogendam, Yoo Young [7 ]
Niessen, Wiro Joep [3 ,4 ,8 ]
Mathijssen, Irene Margreet Jacqueline [1 ]
机构
[1] Erasmus Univ, Med Ctr, Sophia Childrens Hosp, Dept Plast & Reconstruct Surg & Hand Surg,Dutch C, Rotterdam, Netherlands
[2] Erasmus Univ, Med Ctr, Sophia Childrens Hosp, Dept Pediat Radiol,Dutch Craniofacial Ctr, Rotterdam, Netherlands
[3] Erasmus Univ, Dept Radiol, Med Ctr, Rotterdam, Netherlands
[4] Erasmus Univ, Dept Med Informat, Med Ctr, NL-3000 DR Rotterdam, Netherlands
[5] Erasmus Univ, Sophia Childrens Hosp, Med Ctr, Dept Pediat Neurosurg,Dutch Craniofacial Ctr, NL-3000 DR Rotterdam, Netherlands
[6] Erasmus Univ, Dept Biostat, Med Ctr, NL-3000 DR Rotterdam, Netherlands
[7] Erasmus Univ, Dept Epidemiol, Med Ctr, NL-3000 DR Rotterdam, Netherlands
[8] Delft Univ Technol, Fac Sci Appl, NL-2600 AA Delft, Netherlands
关键词
Cerebellum; Craniosynostosis syndromes; Chiari I malformation; Posterior fossa; CRANIAL FOSSA; QUANTITATIVE ASSESSMENT; PRESENTING DEFORMITY; CROUZON SYNDROME; PATHOGENESIS; GROWTH; SEGMENTATION; PREVALENCE; APERT; BASE;
D O I
10.1016/j.jcms.2015.04.001
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: Patients with craniosynostosis syndromes are at risk of increased intracranial pressure (ICP) and Chiari I malformation (CMI), caused by a combination of restricted skull growth, venous hypertension, obstructive sleep apnea (OSA), and an overproduction or insufficient resorption of cerebrospinal fluid. This study evaluates whether craniosynostosis patients with CMI have an imbalance between cerebellar volume (CV) and posterior fossa volume (PFV), that is, an overcrowded posterior fossa. Methods: Volumes were measured in 3D-SPGR TI-weighted MR scans of 28 'not-operated' craniosynostosis patients (mean age: 4.0 years; range: 0-14), 85 'operated' craniosynostosis patients (mean age: 8.0 years; range: 1-18), and 34 control subjects (mean age: 5.4 years; range: 0-15). Volumes and CV/PFV ratios were compared between the operated and not-operated craniosynostosis patients, between the individual craniosynostosis syndromes and controls, and between craniosynostosis patients with and without CMI. Data were logarithmically transformed and studied with analysis of covariance (ANCOVA). Results: The CV, PFV, and CV/PFV ratios of not-operated craniosynostosis patients and operated craniosynostosis patients were similar to those of the control subjects. None of the individual syndromes was associated with a restricted PFV. However, craniosynostosis patients with CMI had a significantly higher CV/PFV ratio than the control group (0.77 vs. 0.75; p = 0.008). The range of CV/PFV ratios for craniosynostosis patients with CMI, however, did not exceed the normal range. Conclusion: Volumes and CV/PFV ratio cannot predict which craniosynostosis patients are more prone to developing CMI than others. Treatment should focus on the skull vault and other contributing factors to increased ICP, including OSA and venous hypertension. (C) 2015 European Association for Cranio-Maxillo-Facial Surgery. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:813 / 819
页数:7
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