Mega Cisterna Magna
Mega Cisterna Magna
Mega Cisterna Magna
Epidemiology
A mega cisterna magna is thought to occur in ~1% of all brains imaged postnatally.
Associations
Especially if noted antenatally, a mega cisterna magna has been associated with:
infarction
inflammation/infection: particularly cytomegalovirus
chromosomal abnormalities: especially trisomy 18
However, when a mega cisterna magna occurs as an isolated finding with normal ventricles the
prognosis is good.
Clinical presentation
There are no specific symptoms related to this condition.
Pathology
Some authors have proposed that mega cisterna magna is a result of a delayed Blake pouch
fenestration; when fenestration does not occur, it results in a Blake pouch cyst 6.
Radiographic features
Ultrasound
In antenates, mega cisterna magna refers to an enlarged retrocerebellar CSF space:
CT/MRI
i
Typically seen as prominent retrocerebellar cerebrospinal fluid (CSF) appearing space with a
normal vermis, normal 4th ventricle, and normal cerebellar hemispheres. An enlarged cisterna
magna usually measures >10 mm on midsagittal images. An enlarged posterior fossa can
sometimes be present 6.
Differential diagnosis
Mega cisterna magna needs to be distinguished from other causes of an enlarged retrocerebellar
CSF space:
arachnoid cyst
epidermoid cyst: often shows a heterogeneous/dirty signal on FLAIR and restricted
diffusion
cerebellar atrophy / cerebellar hypoplasia
Dandy-Walker malformation: vermis not intact
Blake pouch cyst: usually a hydrocephalus is present
pilocytic astrocytoma: if very posterior and predominantly cystic
ii