Department of Neuroradiology, Children's National Hospital, 111 Michigan Ave. NW, Washington, DC, 20010, USA.
Prenatal Pediatrics Institute, Children's National Hospital, Washington, DC, USA.
Pediatr Radiol. 2021 Jul;51(8):1457-1470. doi: 10.1007/s00247-021-04991-3. Epub 2021 Mar 30.
Dandy-Walker malformation and Blake pouch cysts can have overlapping imaging features. The choroid plexus and associated taenia-tela choroidea complex are displaced inferolaterally in Dandy-Walker malformation and below the vermis in Blake pouch cysts.
To determine the normal fetal and postnatal MR appearance of the choroid plexus and taenia-tela choroidea complex, and whether their location can help distinguish Dandy-Walker malformation from Blake pouch cysts.
In this retrospective study, we evaluated brain MR exams from normal-appearing fetuses (gestational age 19-38 weeks) and infants, fetal and postnatal exams in Blake pouch cysts and Dandy-Walker malformation, and ambiguous cases equivocal for mild Dandy-Walker malformation and Blake pouch cysts. We documented choroid plexus and the taenia-tela choroidea complex location and axial and sagittal angles in each case. Then we contrasted and compared the original and updated fetal diagnoses based on taenia-tela choroidea complex and choroid plexus positions.
The choroid plexus location and the taenia-tela choroidea complex location and angles varied significantly among normal exams, Blake pouch cyst exams and Dandy-Walker malformation exams (P<0.01). Dandy-Walker malformation showed inferolateral displacement of the taenia-tela choroidea complex and choroid plexus distant from the vermis. Adding the taenia-tela choroidea complex and choroid plexus into the assessment improved diagnostic accuracy, especially in ambiguous cases.
The location of the taenia-tela choroidea complex and choroid plexus provided additional diagnostic neuroimaging clues that could be used in conjunction with other conventional findings to distinguish Dandy-Walker malformation and Blake pouch cysts. Normal, Blake pouch cyst, and Dandy-Walker malformation cases differed with regard to taenia-tela choroidea complex and choroid plexus position. Inferolateral taenia-tela choroidea complex displacement distant from the vermian margin was characteristic of Dandy-Walker malformation.
Dandy-Walker 畸形和 Blake 囊囊肿在影像学上可能有重叠的特征。脉络丛及其相关的脉络膜带在 Dandy-Walker 畸形中向外侧下方移位,在 Blake 囊囊肿中位于蚓部下方。
确定脉络丛和脉络膜带复合体在正常胎儿和产后的磁共振成像(MR)表现,以及它们的位置是否有助于区分 Dandy-Walker 畸形和 Blake 囊囊肿。
在这项回顾性研究中,我们评估了正常表现的胎儿(胎龄 19-38 周)和婴儿的脑 MR 检查,以及 Blake 囊囊肿和 Dandy-Walker 畸形的胎儿和产后检查,以及对轻度 Dandy-Walker 畸形和 Blake 囊囊肿有疑问的病例。我们记录了脉络丛和脉络膜带复合体的位置,以及每个病例的轴向和矢状角。然后,我们根据脉络膜带复合体和脉络丛的位置对比和比较原始和更新的胎儿诊断。
在正常检查、Blake 囊囊肿检查和 Dandy-Walker 畸形检查中,脉络丛的位置和脉络膜带复合体的位置和角度有显著差异(P<0.01)。Dandy-Walker 畸形表现为脉络膜带复合体和脉络丛向外侧下方的远离蚓部的移位。将脉络膜带复合体和脉络丛纳入评估提高了诊断准确性,尤其是在有疑问的病例中。
脉络膜带复合体和脉络丛的位置提供了额外的神经影像学诊断线索,可以与其他常规发现结合使用,以区分 Dandy-Walker 畸形和 Blake 囊囊肿。正常、Blake 囊囊肿和 Dandy-Walker 畸形病例在脉络膜带复合体和脉络丛的位置上有所不同。远离蚓部边缘的外侧脉络膜带复合体的移位是 Dandy-Walker 畸形的特征。