Siverino Rita Olivia Anna, Guarrera Vincenzo, Attinà Giancarlo, Chiaramonte Rita, Milone Pietro, Chiaramonte Ignazio
University Hospital of Catania, Catania, Italy.
University Hospital of Catania, Catania, Italy
Neuroradiol J. 2015 Apr;28(2):217-21. doi: 10.1177/1971400915581744. Epub 2015 May 11.
We describe a case of atretic cephalocele (AC) characterized by the presence of various cerebral anomalies of different midline structures. In our patient the presence of a parietal AC was associated with an embryonic position of the straight sinus, fenestration of the superior sagittal sinus, an abnormal insertion of the cerebellar tentorium with prominence of the superior cerebellar cistern and a septum pellucidum cyst. These findings, associated with AC, could lead to a worse prognosis with regard to neurodevelopmental milestones. This suggests that even if AC is a benign lesion, a complete evaluation of the brain structures should always be performed in these young patients.
我们描述了一例闭锁性脑膨出(AC)病例,其特征为不同中线结构存在各种脑异常。在我们的患者中,顶叶AC的存在与直窦的胚胎位置、上矢状窦开窗、小脑幕异常插入伴小脑上池突出以及透明隔囊肿有关。这些与AC相关的发现可能导致神经发育里程碑方面的预后更差。这表明,即使AC是一种良性病变,对于这些年轻患者也应始终对脑结构进行全面评估。