1 Department of Radiology and Medical Imaging, Cincinnati Children's Hospital Medical Center, 3333 Burnet Ave, Cincinnati, OH 45229-3026.
2 Department of Pediatric Neurosurgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
AJR Am J Roentgenol. 2018 Dec;211(6):1376-1380. doi: 10.2214/AJR.18.20088. Epub 2018 Oct 17.
The purpose of this study was to examine differences between patients with myelomeningocele and those with myelocele with respect to brain imaging findings at fetal MRI.
A single-center retrospective analysis was performed of fetal MRI examinations revealing open spinal dysraphism from 2004 through 2016 with available diagnostic postnatal spinal MR images in conjunction with neurosurgical follow-up findings. Images were reviewed by two board-certified fellowship-trained pediatric neuroradiologists. Relevant clinical data were recorded.
The study included 119 fetal MRI examinations of patients with open spinal dysraphism. Myeloceles were found in 29.4% (35/119) of these examinations and myelomeningoceles in the others. All (35/35) myeloceles showed grade 3 (severe) Chiari II malformations. Only 73.8% (62/84) of myelomeningoceles showed grade 3 Chiari II malformation. Clinically significant spinal kyphosis was found in 5.0% (6/119) of fetuses, and all of these fetuses had grade 3 Chiari II malformations. The size of the spinal dysraphic defect had significant positive correlation with lateral (p < 0.0001) and third (p = 0.006) ventricular size. Mean volume of the myelomeningocele sac was significantly different among Chiari II grades and inversely proportional to Chiari II grade (p = 0.0009).
Larger spinal dysraphic defects correlated with increased ventricular size at fetal MRI. All of the fetuses with myelocele or kyphosis had severe Chiari II malformations. Larger myelomeningocele sac size was associated with lower grade of Chiari II malformation, suggesting that myelomeningocele sac formation may be protective against hindbrain herniation.
本研究旨在探讨胎儿磁共振成像(MRI)中脊膜脊髓膨出和脊髓脊膜膨出患者的脑影像学表现差异。
对 2004 年至 2016 年间在我院进行的胎儿 MRI 检查进行了单中心回顾性分析,这些检查显示存在开放性脊柱裂畸形,并伴有可获得的诊断性产后脊髓 MRI 图像和神经外科随访结果。由 2 位具有委员会认证的、接受过专业培训的儿科神经放射学专家进行图像审查。记录相关临床数据。
本研究纳入了 119 例胎儿 MRI 检查,这些胎儿均存在开放性脊柱裂畸形。35 例(35/119)检查结果为脊髓脊膜膨出,其余为脊膜脊髓膨出。所有(35/35)脊髓脊膜膨出患者均存在 3 级(严重)Chiari II 畸形。只有 73.8%(62/84)的脊膜脊髓膨出患者存在 3 级 Chiari II 畸形。在 5.0%(6/119)的胎儿中发现了有临床意义的脊柱后凸,这些胎儿均存在 3 级 Chiari II 畸形。脊髓裂畸形缺损的大小与侧脑室(p<0.0001)和第三脑室(p=0.006)大小呈显著正相关。Chiari II 分级之间的脊髓脊膜膨出囊体积存在显著差异,且与 Chiari II 分级呈反比(p=0.0009)。
较大的脊髓裂畸形缺损与胎儿 MRI 中脑室增大相关。所有存在脊髓脊膜膨出或脊柱后凸的胎儿均存在严重的 Chiari II 畸形。较大的脊髓脊膜膨出囊体积与 Chiari II 畸形分级较低相关,这表明脊髓脊膜膨出囊的形成可能对小脑疝出具有保护作用。