Department of Radiology, Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Department of Radiology, Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Pediatr Neurol. 2018 Feb;79:3-7. doi: 10.1016/j.pediatrneurol.2017.09.018. Epub 2017 Oct 9.
The morphology of the skull base can be altered in craniosynostoses. The objective of this study is to evaluate the reduced intercarotid artery distance in the lacerum segment in patients with syndromic and isolated brachycephaly.
The distances between the inner walls of the carotid canal at the lacerum segment were measured on high-resolution CT scans in children with Crouzon (25), Pfeiffer (21), Apert (26), Saethre-Chotzen (7) syndromes, isolated bicoronal synostosis (9), and compared to an age-matched control group (30).
A significantly smaller mean distance between carotid canal walls was observed in Crouzon (11.1 ± 4.9 mm), Pfeiffer (9.6 ± 5.1 mm), Apert (12.3 ± 4.3 mm), Saethre-Chotzen (14.8 ± 3.0 mm) syndromes, and isolated bicoronal synostosis (14.9 ± 3.7 mm) as compared to the control group (19.7 ± 2.4 mm, P < 0.001, P < 0.001, P < 0.001, P = 0.005, and P = 0.002, respectively). There was no statistically significant difference in intercarotid canal distance among the Apert, Saethre-Chotzen and isolated bicoronal synostosis groups. Overall, the brachycephalic group showed reduced intercarotid canal distance comparing to controls (P < 0.001).
There is significant reduction of the distance between carotid canals in brachycephalic patients. This distance is more significantly altered in FGFR-related brachycephaly syndromes (especially Crouzon and Pfeiffer syndromes), than Saethre-Chotzen syndrome (TWIST1 mutation) and isolated non-syndromic bicoronal synostosis. This study highlights the importance of FGFRs in shaping the skull base. Altered vascular course of the internal carotid arteries can have important implications in planning skull base surgery in brachycephalic patients.
颅缝早闭会改变颅底的形态。本研究的目的是评估综合征型和孤立性短头畸形患者颅中窝段颈动脉内距减小的情况。
对 25 例 Crouzon 综合征、21 例 Pfeiffer 综合征、26 例 Apert 综合征、7 例 Saethre-Chotzen 综合征、9 例单纯性冠状缝早闭和 30 例年龄匹配的对照组儿童的高分辨率 CT 扫描中颈动脉管裂段的内管壁之间的距离进行了测量。
与对照组(19.7±2.4mm,P<0.001,P<0.001,P<0.001,P=0.005 和 P=0.002)相比,Crouzon 综合征(11.1±4.9mm)、Pfeiffer 综合征(9.6±5.1mm)、Apert 综合征(12.3±4.3mm)、Saethre-Chotzen 综合征(14.8±3.0mm)和单纯性冠状缝早闭组(14.9±3.7mm)的颈动脉管壁之间的平均距离明显较小。Apert 综合征、Saethre-Chotzen 综合征和单纯性冠状缝早闭组之间的颈内动脉管距离无统计学差异。总体而言,与对照组相比,短头畸形组的颈内动脉管距离减小(P<0.001)。
短头畸形患者的颈动脉管之间的距离明显减小。在 FGFR 相关的短头畸形综合征(尤其是 Crouzon 和 Pfeiffer 综合征)中,这种距离的改变比 Saethre-Chotzen 综合征(TWIST1 突变)和单纯性非综合征性冠状缝早闭更为显著。本研究强调了 FGFR 在塑造颅底方面的重要性。颈内动脉血管走行的改变在计划短头畸形患者的颅底手术时具有重要意义。