“…They constitute approximately 1% of all intracranial space-occupying lesions [ 1 , 3 - 5 ]. Most ACs are indolent lesions that remain asymptomatic until they are found incidentally after neuroimaging for an unrelated problem [ 4 , 6 - 7 ]; however, ACs can be the source of headaches, increased head circumference, and developmental delay in pediatric patients; rarely, they can cause weakness, seizures, or psychiatric alterations [ 1 ]. Complications associated with ACs concern their continued growth, which can exacerbate headaches, create a focal neurological deficit or, particularly with suprasellar and quadrigeminal ACs, also result in obstructive hydrocephalus or brainstem compression, which can be life-threatening [ 1 , 8 ].…”