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Diffusion tensor imaging evaluation of white matter in adolescents with myelomeningocele and Chiari II malformation.弥散张量成像评估脊髓脊膜膨出伴 Chiari II 畸形青少年的脑白质。
Pediatr Radiol. 2011 Nov;41(11):1407-15. doi: 10.1007/s00247-011-2180-6. Epub 2011 Jul 2.
2
Reduced anisotropy in the middle cerebellar peduncle in Chiari-II malformation.小脑脑桥脚在 Chiari-II 畸形中的各向异性降低。
Cerebellum. 2010 Sep;9(3):303-9. doi: 10.1007/s12311-010-0162-0.
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Longitudinal diffusion-weighted imaging in infants with hydrocephalus: decrease in tissue water diffusion after cerebrospinal fluid diversion.脑积水婴儿的纵向扩散加权成像:脑脊液分流后组织水扩散降低
J Neurosurg Pediatr. 2009 Jul;4(1):56-63. doi: 10.3171/2009.3.PEDS08337.
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White matter microstructural abnormalities in children with spina bifida myelomeningocele and hydrocephalus: a diffusion tensor tractography study of the association pathways.脊柱裂脊髓脊膜膨出合并脑积水患儿的白质微观结构异常:联合通路的扩散张量纤维束成像研究
J Magn Reson Imaging. 2008 Apr;27(4):700-9. doi: 10.1002/jmri.21297.
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Diffusion-weighted imaging in normal fetal brain maturation.正常胎儿脑成熟过程中的扩散加权成像
Eur Radiol. 2007 Sep;17(9):2422-9. doi: 10.1007/s00330-007-0634-x. Epub 2007 Apr 3.
6
MRI of normal fetal brain development.正常胎儿脑发育的磁共振成像
Eur J Radiol. 2006 Feb;57(2):199-216. doi: 10.1016/j.ejrad.2005.11.020. Epub 2006 Jan 4.
7
Spinal lesion level in spina bifida: a source of neural and cognitive heterogeneity.脊柱裂中的脊髓病变水平:神经和认知异质性的一个来源。
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Fiber tract-based atlas of human white matter anatomy.基于纤维束的人类白质解剖图谱。
Radiology. 2004 Jan;230(1):77-87. doi: 10.1148/radiol.2301021640. Epub 2003 Nov 26.
9
The Chiari II malformation: cause and impact.Chiari II型畸形:病因与影响。
Childs Nerv Syst. 2003 Aug;19(7-8):540-50. doi: 10.1007/s00381-003-0792-3. Epub 2003 Aug 12.
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Isotropic apparent diffusion coefficient mapping of postnatal cerebral development.出生后大脑发育的各向同性表观扩散系数映射
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小脑 Chiari II 畸形胎儿的弥散加权成像。

Diffusion-weighted imaging of the cerebellum in the fetus with Chiari II malformation.

机构信息

Division of Neuroradiology, Department of Diagnostic Imaging, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

出版信息

AJNR Am J Neuroradiol. 2013 Aug;34(8):1656-60. doi: 10.3174/ajnr.A3468. Epub 2013 May 30.

DOI:10.3174/ajnr.A3468
PMID:23721901
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8051439/
Abstract

BACKGROUND AND PURPOSE

Diffusion-weighted imaging can be used to characterize brain maturation. MR imaging of the fetus is used in cases of suspected Chiari II malformation when further evaluation of the posterior fossa is required. We sought to investigate whether there were any quantitative ADC abnormalities of the cerebellum in fetuses with this malformation.

MATERIALS AND METHODS

Measurements from ROIs acquired in each cerebellar hemisphere and the pons were obtained from calculated ADC maps performed on our Avanto 1.5T imaging system. Values in groups of patients with Chiari II malformations were compared with those from fetuses with structurally normal brains, allowing for the dependent variable of GA by using linear regression analysis.

RESULTS

There were 8 fetuses with Chiari II malformations and 23 healthy fetuses, ranging from 20 to 31 GW. There was a significant linear decline in the cerebellar ADC values with advancing gestation in our healthy fetus group, as expected. The ADC values of the cerebellum of fetuses with Chiari II malformation were higher [1820 (±100) × 10⁻⁶ mm²/s] than ADC values in the healthy fetuses (1370 ± 70) × 10⁻⁶ mm²/s. This was statistically significant, even when allowing for the dependent variable of GA (P = .0126). There was no significant difference between the pons ADC values in these groups (P = .645).

CONCLUSIONS

While abnormal white matter organization or early cerebellar degeneration could potentially contribute to our findings, the most plausible explanation pertains to abnormalities of CSF drainage in the posterior fossa, with increased extracellular water possibly accounting for this phenomenon.

摘要

背景与目的

弥散加权成像可用于脑成熟度的特征描述。当需要进一步评估后颅窝时,胎儿磁共振成像可用于 Chiari II 畸形的疑似病例。我们试图研究小脑在存在这种畸形的胎儿中是否存在定量 ADC 异常。

材料与方法

在我们的 Avanto 1.5T 成像系统上进行计算 ADC 图,从每个小脑半球和脑桥获得的 ROI 测量值。通过线性回归分析,将 Chiari II 畸形患者组与结构正常脑的胎儿组的变量进行比较。

结果

共有 8 例 Chiari II 畸形胎儿和 23 例正常胎儿,胎龄范围为 20 至 31 周。正如预期的那样,在正常胎儿组中,随着胎龄的增加,小脑 ADC 值呈明显线性下降。Chiari II 畸形胎儿的小脑 ADC 值(1820±100)×10⁻⁶mm²/s高于正常胎儿(1370±70)×10⁻⁶mm²/s,具有统计学意义,即使考虑胎龄的依赖变量(P=0.0126)。这些组之间的脑桥 ADC 值无显著差异(P=0.645)。

结论

虽然异常的白质组织或早期小脑退化可能导致我们的发现,但最合理的解释与后颅窝 CSF 引流异常有关,可能是细胞外水增加导致了这种现象。