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因囟骨导致前囟门缺失。

Absence of the anterior fontanelle due to a fontanellar bone.

作者信息

Woods Roger H, Johnson David

机构信息

Oxford Craniofacial Unit, John Radcliffe Hospital, Oxford, United Kingdom.

出版信息

J Craniofac Surg. 2010 Mar;21(2):448-9. doi: 10.1097/SCS.0b013e3181cfe970.

Abstract

Improved accessibility to supraregional centers in the United Kingdom has led to an increased referral of minor craniofacial anomalies. We have recognized a group of patients referred with absence of the anterior fontanelle and possible associated craniosynostosis. The aim of this study was to assess the group of patients in which the anterior fontanelle was entirely replaced by a single bone, examining associations, relationship to craniosynostosis, and prognostic implications.Eleven patients had fontanellar bones replacing the anterior fontanelle on computed tomographic imaging in the 3-year study period. Five were referred solely because of absence of the anterior fontanelle; and the remainder, because of concern of concomitant craniosynostosis. Five children had associated craniosynostosis (sagittal synostosis, 3; metopic synostosis, 1; and bicoronal synostosis, 1), 1 had acrocallosal syndrome, and 5 had no other craniofacial abnormalities. The patient group with craniosynostosis have been managed in line with the unit protocol and have good early postoperative results (mean postoperative follow-up, 9.4 mo). The 5 patients who had an anterior fontanellar bone as an isolated finding were observed and have developed normally with a mean follow-up of 2 years 1.4 months (range, 8 mo to 3 y 4 mo).Replacement of the anterior fontanelle with a fontanellar bone is an uncommon finding, often associated with craniosynostosis. Cases with craniosynostosis can be treated in line with unit protocols. Isolated anterior fontanellar bones can be managed conservatively without adverse impact on the child.

摘要

英国超区域中心就医便利性的提高导致了小儿颅面畸形转诊量的增加。我们发现了一组因前囟门缺失及可能相关的颅缝早闭而前来转诊的患者。本研究的目的是评估前囟门完全被单一骨替代的患者群体,研究其关联情况、与颅缝早闭的关系以及预后影响。

在为期3年的研究期间,11例患者的计算机断层扫描成像显示前囟门被囟门骨替代。5例仅因前囟门缺失前来就诊;其余患者则是因担心合并颅缝早闭。5例儿童合并颅缝早闭(矢状缝早闭3例、额缝早闭1例、双冠状缝早闭1例),1例患有胼胝体发育不全综合征,5例无其他颅面异常。合并颅缝早闭的患者组已按照科室方案进行治疗,术后早期效果良好(术后平均随访9.4个月)。5例仅发现前囟门骨的患者接受了观察,平均随访2年1.4个月(范围8个月至3年4个月),发育正常。

前囟门被囟门骨替代是一种罕见的情况,常与颅缝早闭相关。合并颅缝早闭的病例可按照科室方案进行治疗。孤立的前囟门骨可进行保守处理,对儿童无不良影响。

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