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Arachnoid Cyst ( Localized Pseudotumor ) This lesion, which is probably congenital, presents clinically at all ages but may become evident only in adult life, when it gives rise to symptoms of increased intracranial pressure and sometimes to focal cerebral or cerebellar signs, simulating intracranial neoplasm. Seizures may occur but are not characteristic; we have seen only one instance. In infants and young children, macrocrania and extensive unilateral transillumination are characteristic features. Usually these cysts overlie the sylvian ssure; occasionally they are interhemispheric under the frontal lobes or lie in the pineal region or under the cerebellum. They may attain a large size, to the point of enlarging the middle fossa and elevating the lesser wing of the sphenoid, but they do not communicate with the ventricle. Rarely, one of these cysts may cover the entire surface of both cerebral hemispheres and create a so-called external hydrocephalus (page 533). The cysts are readily recognized (often accidentally) on the nonenhanced CT scan or MRI, showing a circumscribed tissue defect lled with uid that has the density of CSF (Gandy and Heier). If these cysts are completely asymptomatic, they should be left alone; if symptomatic, additional (MRI) studies are indicated, so as not to overlook a chronic subdural hematoma, which is often associated and may not be visualized on the unenhanced CT scan. Suprasellar arachnoid cysts are discussed further on (page 577). The treatment of enlarging and symptomatic cysts is marsupialization or, less preferably, by shunting from the cyst to the subarachnoid space. javascript pdf editor free PDFKit
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