Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Prenat Diagn. 2012 Jan;32(1):75-82. doi: 10.1002/pd.2911.
The purpose of this study was to describe the relationship between intracranial and extracranial anomalies and neurodevelopmental outcome for fetuses diagnosed with a posterior fossa anomaly (PFA) on fetal MRI.
Cases of Dandy-Walker malformation, vermian hypogenesis/hypoplasia, and mega cisterna magna (MCM) were identified through the Fetal Care Center of Cincinnati between January 2004 and December 2010. Parental interview and retrospective chart review were used to assess neurodevelopmental outcome.
Posterior fossa anomalies were identified in 59 fetuses; 9 with Dandy-Walker malformation, 36 with vermian hypogenesis/hypoplasia, and 14 with MCM. Cases with isolated PFAs (14/59) had better outcomes than those with additional anomalies (p = 0.00016), with isolated cases of MCM all being neurodevelopmentally normal. Cases with additional intracranial anomalies had a worse outcome than those without intracranial anomalies (p = 0.00017). The presence of extracranial anomalies increased the likelihood of having a poor outcome (p = 0.00014) as did the identification of an abnormal brainstem (p = 0.00018).
Intracranial and extracranial anomalies were good predictors of neurodevelopmental outcome in this study. The prognosis was poor for individuals with an abnormal brainstem, whereas those with isolated MCM had normal neurodevelopmental outcome.
本研究旨在描述胎儿磁共振成像(MRI)诊断为后颅窝异常(PFA)的胎儿颅内和颅外异常与神经发育结局之间的关系。
通过辛辛那提胎儿保健中心,于 2004 年 1 月至 2010 年 12 月期间,确定了 Dandy-Walker 畸形、蚓部发育不全/发育不良和巨大第四脑室(MCM)病例。通过父母访谈和回顾性图表审查评估神经发育结局。
在 59 例胎儿中发现了后颅窝异常;9 例 Dandy-Walker 畸形,36 例蚓部发育不全/发育不良,14 例 MCM。单纯 PFAs(14/59)的病例比伴有其他异常的病例(p=0.00016)结局更好,单纯 MCM 的病例均神经发育正常。伴有其他颅内异常的病例比没有颅内异常的病例(p=0.00017)的结局更差。存在颅外异常增加了不良结局的可能性(p=0.00014),异常脑干的存在也是如此(p=0.00018)。
在本研究中,颅内和颅外异常是神经发育结局的良好预测因素。异常脑干的患者预后较差,而孤立性 MCM 的患者神经发育正常。