Taylor G A, Sanders R C
AJNR Am J Neuroradiol. 1983 Nov-Dec;4(6):1203-6.
The sonographic appearance of the Dandy-Walker malformation is not well known. Experience with sonography in the recognition of the Dandy-Walker syndrome in four neonates is presented. Three cases were discovered serendipitously: one during obstetric evaluation for uncertain gestational age and two in asymptomatic neonates. The typical sonographic features are a triangular posterior fossa cyst, a dilated aqueduct of Sylvius in communication with the cyst, elevation and hypoplasia of the cerebellum, and variable dilatation of the third and lateral ventricles. Sonography is often the first diagnostic procedure performed on these patients and can be very useful in recognizing the anomaly.
丹迪-沃克畸形的超声表现尚不为人熟知。本文介绍了对4例新生儿进行超声检查以识别丹迪-沃克综合征的经验。3例为偶然发现:1例在产科评估孕周不确定时发现,2例在无症状新生儿中发现。典型的超声特征为三角形后颅窝囊肿、与囊肿相通的扩张的中脑导水管、小脑抬高和发育不全,以及第三脑室和侧脑室不同程度的扩张。超声检查通常是对这些患者进行的首个诊断程序,对识别该异常非常有用。