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颅骨冠状缝关节的自然史和发病机制:对理解克鲁宗颅骨狭窄症缺陷发病机制的启示

The natural history and pathogenesis of the cranial coronal ring articulations: implications in understanding the pathogenesis of the Crouzon craniostenotic defects.

作者信息

Burdi A R, Kusnetz A B, Venes J L, Gebarski S S

出版信息

Cleft Palate J. 1986 Jan;23(1):28-39.

PMID:3455900
Abstract

The craniostenotic birth defects seen in patients with Crouzon syndrome have prompted this developmental study on the system of articulations between the human frontal, sphenoid, and ethmoid bones. The Crouzon facies, including midfacial hypoplasia and exorbitism, have been linked to the premature synostosis of calvarial sutures. However, considerable evidence shows that midfacial positioning is linked to increasing length of the midline cranial base. Thirty-seven typical-for-age (8 to 29 weeks) embryos were histologically prepared, read serially, and three-dimensionally reconstructed to map the so-called coronal ring articulations that continuously join the frontal, sphenoid, and ethmoid bones. A morphologic staging plan was used to show the progressive development of bones and intervening joints. Data show that a coronal ring exists beginning at 8 weeks. Those portions of the ring separating the frontal and sphenoid bones (within the orbit and laterally along the coronal suture) show the typical structure of a five-layered suture. This sutural component of the ring is C-shaped with a cartilaginous bridge between the optic foramina completing the ring. This is the sphenoethmoidal (S-E) synchondrosis of the midline cranial base. It is suggested that this deeply located cartilage joint is the primary site of pathogenesis in the craniostenotic facies and not the coronal sutures which are operated upon. Even though the S-E cartilage would be difficult and potentially morbid to approach surgically, this study would suggest that preoperative computed tomography (CT) of the skull base with special emphasis on the S-E region may provide a better prognosis regarding midface growth effects after surgery. It appears to be the fused S-E synchondrosis and not necessarily the premature closure of the coronal sutures that may tether the midface posteriorly.

摘要

克鲁宗综合征患者出现的颅缝早闭出生缺陷促使了对人类额骨、蝶骨和筛骨之间关节系统的这项发育研究。克鲁宗面容,包括面中部发育不全和眼球突出,与颅盖缝过早融合有关。然而,大量证据表明面中部定位与中线颅底长度增加有关。对37例年龄典型(8至29周)的胚胎进行组织学制备、连续读取并进行三维重建,以绘制连续连接额骨、蝶骨和筛骨的所谓冠状环关节。使用形态学分期方案来展示骨骼和中间关节的渐进发育。数据显示冠状环在8周时就已存在。冠状环中分隔额骨和蝶骨的部分(在眼眶内以及沿冠状缝外侧)呈现出典型的五层缝结构。环的这个缝组件呈C形,视神经孔之间有软骨桥完成环的连接。这就是中线颅底的蝶筛(S-E)软骨结合。研究表明,这个位置较深的软骨关节是颅缝早闭面容发病机制的主要部位,而非接受手术的冠状缝。尽管S-E软骨在手术中难以接近且可能存在风险,但这项研究表明,术前对头颅底部进行计算机断层扫描(CT),特别关注S-E区域,可能会为手术后中面部生长效应提供更好的预后。似乎是融合的S-E软骨结合,而不一定是冠状缝过早闭合,可能会向后牵拉中面部。

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