From the Departments of Radiology and Medical Imaging (U.D.N., B.M.K.-F.)
University of Cincinnati College of Medicine (U.D.N., B.M.K.-F., P.S.H., C.V.), Cincinnati, Ohio.
AJNR Am J Neuroradiol. 2021 Sep;42(9):1716-1721. doi: 10.3174/ajnr.A7215. Epub 2021 Jul 15.
Dandy-Walker malformation, vermian hypoplasia, and Blake pouch remnant represent a continuum of anomalies and are common reasons for referral for fetal MR imaging. This study aimed to determine biometric measurements that quantitatively delineate these 3 posterior fossa phenotypes.
Our single-center institutional review board approved a retrospective analysis of all fetal MRIs for posterior fossa malformations, including Dandy-Walker malformation, vermian hypoplasia, and Blake pouch remnant. Measurements included the anterior-to-posterior pons, craniocaudal and anterior-to-posterior vermis, lateral ventricle size, and tegmentovermian and posterior fossa angles. Measurements were compared with normal biometry and also between each subgroup.
Thirty-three fetuses met the criteria and were included in the study. Seven were designated as having Dandy-Walker malformation; 16, vermian hypoplasia; and 10, Blake pouch remnant. No significant group interactions with adjusted mean gestational age for tegmentovermian and posterior fossa angles were observed. The tegmentovermian angle was significantly higher in Dandy-Walker malformation (109.5° [SD, 20.2°]) compared with vermian hypoplasia (52.13° [SD, 18.8°]) and Blake pouch remnant (32.1° [SD, 17.9°]), regardless of gestational age. Lateral ventricle sizes were significantly higher in Dandy-Walker malformation at a mean of ≥23.1 weeks' gestational age compared with vermian hypoplasia and Blake pouch remnant. The anterior-to-posterior and craniocaudal vermes were significantly smaller in Dandy-Walker malformation compared with vermian hypoplasia and Blake pouch remnant at mean of ≥23.1 weeks' gestational age.
Dandy-Walker malformation can be described in relation to vermian hypoplasia and Blake pouch remnant by an increased tegmentovermian angle; however, other potential qualifying biometric measurements are more helpful at ≥23.1 weeks' gestational age. Because they fall along the same spectrum of abnormalities, the difficulty in distinguishing these entities from one another makes precise morphologic and biometric descriptions important.
Dandy-Walker 畸形、蚓部发育不全和 Blake 袋残余代表了一系列异常,并是胎儿磁共振成像(MRI)检查的常见指征。本研究旨在确定定量描绘这 3 种后颅窝表型的影像学参数。
我们对所有因后颅窝畸形行胎儿 MRI 检查的患者进行了单中心回顾性分析,包括 Dandy-Walker 畸形、蚓部发育不全和 Blake 袋残余。测量参数包括桥前-后孔、颅尾和前后蚓部、侧脑室大小以及桥脑-蚓部和后颅窝角度。我们将测量结果与正常胎儿的参数进行比较,并对各个亚组之间进行比较。
33 例胎儿符合入组标准,纳入本研究。7 例被诊断为 Dandy-Walker 畸形,16 例为蚓部发育不全,10 例为 Blake 袋残余。未观察到桥脑-蚓部和后颅窝角度的组间交互作用与调整后的平均孕龄之间存在显著差异。Dandy-Walker 畸形组的桥脑-蚓部角度(109.5°[标准差,20.2°])显著高于蚓部发育不全组(52.13°[标准差,18.8°])和 Blake 袋残余组(32.1°[标准差,17.9°]),与孕龄无关。在平均≥23.1 孕周时,Dandy-Walker 畸形的侧脑室大小明显大于蚓部发育不全和 Blake 袋残余。在平均≥23.1 孕周时,Dandy-Walker 畸形的前后蚓部明显小于蚓部发育不全和 Blake 袋残余。
Dandy-Walker 畸形可通过增加桥脑-蚓部角度与蚓部发育不全和 Blake 袋残余进行描述;然而,在≥23.1 孕周时,其他潜在的定量测量更有助于诊断。由于它们处于同一异常谱系中,因此彼此之间的鉴别较为困难,因此准确的形态和影像学参数描述非常重要。