Calandrelli Rosalinda, D'Apolito Gabriella, Panfili Marco, Massimi Luca, Caldarelli Massimo, Colosimo Cesare
Institute of Radiology, Università Cattolica Sacro Cuore, L.go A. Gemelli 8, 00168, Rome, Italy.
Institute of Neurosurgery, Università Cattolica Sacro Cuore, L.go A. Gemelli 8, 00168, Rome, Italy.
Childs Nerv Syst. 2016 Mar;32(3):451-9. doi: 10.1007/s00381-015-2956-3. Epub 2015 Nov 16.
This study aimed to explain the functional role of lambdoid arch sutures in the development of cerebellar tonsillar herniation. Posterior cranial fossa (PCF) changes were investigated in infants with premature synostosis of the major and minor sutures of the lambdoid arch without premature synostosis of the PCF synchondroses.
Morphometric and volumetric PCF measurements were performed on preoperative high-resolution CT studies in 12 infants with multisutural craniosynostosis involving the lambdoid arch and compared with those of 12 age-matched healthy subjects.
All 12 patients had hypoplasia of PCF bone structures and normal volumes of the PCF and neural structures. PCF hypoplasia was related to exocciput length in infants with isolated involvement of major sutures, while it was related to posterior skull base hemifossae in infants with isolated involvement of minor lambdoid arch sutures. Foramen magnum AP diameter was reduced in babies with major suture involvement and tonsillar herniation, while foramen magnum AP and LL diameters were reduced in babies with minor suture involvement without tonsillar herniation. Right and left jugular foramen (JF) areas differed in all infants; however, the area of the smaller JF was significantly reduced only in infants with involvement of minor lambdoid arch sutures.
Hypoplasia of PCF bone structures due to sutural synostosis of the lambdoid arch is a required predisposing but not sufficient factor for the development of cerebellar tonsillar herniation through the foramen magnum. Normal PCF volume and foramen magnum anatomy may partly explain the development of cerebellar tonsil herniation in infants with lambdoid arch synostosis.
本研究旨在解释人字缝在小脑扁桃体疝形成过程中的功能作用。对人字缝大小缝过早融合而颅后窝软骨联合未过早融合的婴儿,研究其颅后窝(PCF)的变化。
对12例累及人字缝的多缝颅缝早闭婴儿进行术前高分辨率CT研究,测量PCF的形态学和容积,并与12例年龄匹配的健康受试者进行比较。
12例患者均有PCF骨结构发育不全,但PCF和神经结构容积正常。单纯主要缝受累的婴儿,PCF发育不全与枕外隆凸长度有关;单纯人字缝小缝受累的婴儿,PCF发育不全与后颅底半侧颅窝有关。主要缝受累且有扁桃体疝的婴儿,枕大孔前后径减小;小缝受累但无扁桃体疝的婴儿,枕大孔前后径和内外径均减小。所有婴儿左右颈静脉孔(JF)面积均有差异;然而,仅在人字缝小缝受累的婴儿中,较小JF的面积显著减小。
人字缝过早融合导致的PCF骨结构发育不全是经枕大孔形成小脑扁桃体疝的必要易感因素,但不是充分因素。PCF容积正常和枕大孔解剖结构正常可能部分解释了人字缝过早融合婴儿小脑扁桃体疝的形成。