Abstract：
This case report demonstrates a rare finding of a pediatric patient with Morning Glory anomaly and Moyamoya Disease with a palatal meningeal hamartoma discovered as a mass within a previously repaired incomplete cleft of the alveolus. Oral meningeal hamartomas are exceedingly rare with only two palatal cases described and none within a cleft palate or alveolus. These findings prompt a review of oral hamartomas with meningeal subclassification. Further discussion describes the relationship of the proposed origins of meningeal hamartomas within the setting of cleft palate development.
摘要：
此病例报告显示了罕见的发现，患有晨光异常和Moyamoya病的小儿患者在先前修复的肺泡不完全裂隙中发现了pal膜错构瘤。口腔脑膜错构瘤极为罕见，仅描述了2例，并且在c裂或肺泡内均未出现。这些发现促使人们对具有脑膜亚分类的口腔错构瘤进行回顾。进一步的讨论描述了left裂发育背景下脑膜错构瘤的拟议起源之间的关系。
