Trigylidas T, Baronia B, Vassilyadi M, Ventureyra E C G
Division of Neurosurgery, Children's Hospital of Eastern Ontario, University of Ottawa, 401 Smyth Road, Ottawa, ON K1H 8L1, Canada.
Childs Nerv Syst. 2008 Mar;24(3):329-36. doi: 10.1007/s00381-007-0432-4. Epub 2007 Jul 27.
Chiari I malformations (CMI) involve pathological hindbrain abnormalities reported to be correlated with a hypoplastic posterior fossa. CMI was traditionally characterized by the downward herniation of the cerebellar tonsils with a descent of 5 mm or more below the foramen magnum. The fullness of the cisterna magna and CSF flow at the level of the cervicomedullary junction have been shown to be more useful in selecting symptomatic patients for surgical decompression. The present study calculates posterior fossa dimension and volume estimates in pediatric patients using magnetic resonance imaging. The combination of neuroradiological and clinical findings is used to re-examine the criteria used for diagnosis and treatment of pediatric CMI patients.
A retrospective chart review was conducted on patients who were admitted to the Division of Neurosurgery of the Children's hospital of Eastern Ontario between 1990 and 2007. Clinical and radiological assessments were performed on all patients. Posterior fossa volumes (PFV) and intracranial volumes (ICV) were measured from sagittal head magnetic resonance imaging scans using the Cavalieri method.
Sixty-one CMI patients were identified. There were 32 male and 29 female patients with a mean age of 10 years (range: 8 weeks-18 years). Thirty-four (55%) of these patients were symptomatic with scoliosis (38%), suboccipital headaches (29%), and motor/sensory deficits (26%) being the most prominent symptoms. The mean PFV/ICV ratio for all the CMI patients (0.110) was found to be statistically smaller than that of the control patients (0.127, p=0.022). Mean PFV/ICV ratios for asymptomatic and symptomatic CMI patients were found to be similar for children aged 0-9 years (p=0.783) but different for children aged 10-18 years (p=0.018).
Mean PFV values were found to be smaller in pediatric CMI patients than control patients; this complements earlier studies in adults and supports the present theory concerning the pathophysiological mechanism of CMI. Subtle morphometric differences among asymptomatic and symptomatic patients aged 0-9 years stress the importance of monitoring asymptomatic patients for the onset of symptoms in their adult years. Symptom development in CMI is likely multifactorial and is much more extensive than the degree of cerebellar tonsillar herniation.
Chiari I 畸形(CMI)涉及病理性后脑异常,据报道与后颅窝发育不全相关。传统上,CMI 的特征是小脑扁桃体向下疝出,低于枕骨大孔 5 毫米或更多。已证明枕大池饱满度和颈髓交界处的脑脊液流动情况在选择有症状的患者进行手术减压时更有用。本研究使用磁共振成像计算儿科患者的后颅窝尺寸和体积估计值。结合神经放射学和临床发现,重新审视用于诊断和治疗儿科 CMI 患者的标准。
对 1990 年至 2007 年期间安大略东部儿童医院神经外科收治的患者进行回顾性病历审查。对所有患者进行临床和放射学评估。使用 Cavalieri 方法从矢状位头部磁共振成像扫描测量后颅窝体积(PFV)和颅内体积(ICV)。
确定了 61 例 CMI 患者。有 32 例男性和 29 例女性患者,平均年龄为 10 岁(范围:8 周 - 18 岁)。其中 34 例(55%)患者有症状,脊柱侧弯(38%)、枕下头痛(29%)和运动/感觉障碍(26%)是最突出的症状。发现所有 CMI 患者的平均 PFV/ICV 比值(0.110)在统计学上小于对照组患者(0.127,p = 0.022)。发现 0 - 9 岁儿童无症状和有症状的 CMI 患者的平均 PFV/ICV 比值相似(p = 0.783),但 10 - 18 岁儿童不同(p = 0.018)。
发现儿科 CMI 患者的平均 PFV 值小于对照组患者;这补充了早期对成人的研究,并支持了关于 CMI 病理生理机制的现有理论。0 - 9 岁无症状和有症状患者之间细微的形态计量学差异强调了监测无症状患者成年后症状发作的重要性。CMI 中的症状发展可能是多因素的,并且比小脑扁桃体疝出的程度更为广泛。