Mohr G, Hoffman H J, Munro I R, Hendrick E B, Humphreys R P
Neurosurgery. 1978 Mar-Apr;2(2):83-92. doi: 10.1227/00006123-197803000-00001.
From 1955 to 1975, 116 patients with unilateral and bilateral coronal synostosis, including 39 with craniofacial dysmorphism, were treated surgically. Five techniques were used: multiple linear craniectomies, linear craniectomies with supraorbital grafting, morcellation craniotomies, lateral canthal advancement of the supraorbital margin, and radical cranio-orbitofacial reconstruction. Analysis of clinical and radiological indices of the synostotic process, coupled with evaluation of the surgical results, indicates that the anterior skull base is the site of origin of the bony dysplasia. Therefore, early creation of artificial sutures in the skull base is recommended to provide adequate expansion of the frontal bones and consequently of the entire facial skeleton.
1955年至1975年期间,对116例单侧和双侧冠状缝早闭患者进行了手术治疗,其中39例伴有颅面畸形。采用了五种技术:多处线性颅骨切除术、带眶上植骨的线性颅骨切除术、碎骨片颅骨切开术、眶上缘外眦前移术和根治性颅眶面重建术。对缝早闭过程的临床和放射学指标进行分析,并结合手术结果评估,表明前颅底是骨发育异常的起源部位。因此,建议早期在颅底创建人工缝线,以充分扩张额骨,进而扩张整个面部骨骼。