Intracranial epidermoid cysts are relatively common congenital lesions
which account for about 1% of all intracranial tumours. They result from
inclusion of ectodermal elements during neural tube closure, and
typically present in middle age due to mass effect on adjacent
structures. Their content, derived from desquamated epithelial cells,
mimics CSF on CT and MRI, with the exception of DWI which demonstrates
restricted diffusion. Management is surgical and prognosis is good.
Although predominantly congenital, epidermoid cysts are usually very
slow growing and as such take many years to present. Typically patients
are between 20 and 40 years of age 6. There may be increased prevalence
in males, although this is not found in all series 5-6.
Epidermoid cysts account for approximately 1% of all intracranial tumours 2,8.
An uncommon association exists with anorectal anomalies, sacral anomalies and presacral mass, and is known as the Currarino triad
Epidermoid cysts account for approximately 1% of all intracranial tumours 2,8.
An uncommon association exists with anorectal anomalies, sacral anomalies and presacral mass, and is known as the Currarino triad
Comments
Post a Comment