Mathijssen Irene M J, van der Meulen Jacques J N M, van Adrichem Léon N A, Vaandrager J Michiel, van der Hulst René R W J, Lequin Maarten H, Vermeij-Keers Christl
Department of Plastic and Reconstructive Surgery, Erasmus MC, University Medical Centre, Dr. Molewaterplein 60, 3015 GJ Rotterdam, The Netherlands.
Pediatr Radiol. 2008 Apr;38(4):431-7. doi: 10.1007/s00247-008-0750-z. Epub 2008 Jan 26.
Isolated synostosis of the frontosphenoidal suture is very rare and difficult to diagnose. Little has been reported on the clinical presentation and fetal development of this suture.
To understand the development of the frontosphenoidal suture and the outcome of its synostosis.
We studied the normal fetal development of the frontosphenoidal suture in dry human skulls and the clinical features of four patients with isolated synostosis of the frontosphenoidal suture.
The frontosphenoidal suture develops relatively late during the second trimester of pregnancy, which explains the mild phenotype when there is synostosis. This rare craniosynostosis results in a deformity that causes recession of the lateral part of the frontal bone and supraorbital rim, with minimal facial asymmetry. Three-dimensional CT is the best examination to confirm the diagnosis.
Isolated frontosphenoidal synostosis should be considered in patients with unilateral flattening of the forehead at birth that does not improve within the first few months of life.
额蝶缝孤立性骨性融合非常罕见且难以诊断。关于该缝的临床表现和胎儿发育情况报道较少。
了解额蝶缝的发育及其骨性融合的结局。
我们研究了干燥人颅骨中额蝶缝的正常胎儿发育情况以及4例额蝶缝孤立性骨性融合患者的临床特征。
额蝶缝在妊娠中期相对较晚发育,这解释了发生骨性融合时表型较轻的原因。这种罕见的颅缝早闭导致一种畸形,引起额骨外侧部分和眶上缘后缩,面部不对称轻微。三维CT是确诊的最佳检查方法。
对于出生时单侧前额扁平且在出生后最初几个月内无改善的患者,应考虑孤立性额蝶缝骨性融合。