It should be distinguished from cranial meningocele in which the lesion contains only meninges, and from extracranial brain herniation in which brain herniates through a dural and skull defect (e.g. post-trauma or surgery).
They are thought to occur in one of every 4,000 live births. Frontoethmoidal encephaloceles are more common in the south and south-east Asian populations. There is no recognized gender predilection.
Most cases tend to be sporadic.
Occipital encephaloceles may be associated with a number of additional abnormalities:
Frontoethmoidal encephaloceles manifest as a clinically visible mass along with the nose. The intracranial root of most frontoethmoidal encephaloceles lies at the foramen cecum, a small ostium located at the bottom of a small depression anterior to the crista galli and formed by the closure of the frontal and ethmoid bones.
Basal encephaloceles are internal and are not generally externally visible, although they may manifest as a lump or bump in the oropharynx or nasopharynx.
Small temporal encephaloceles are increasingly recognized as causes of refractory epilepsy in some individuals and are also encountered as asymptomatic sequelae of idiopathic intracranial hypertension.
Encephaloceles, when congenital (most common) are a form of neural tube defect and occur due to a failure of fusion during embryogenesis of the cartilaginous neurocranium, the membranous neurocranium or viscerocranium .
In adults, encephaloceles are mainly due to traumatic or iatrogenic causes but are also increasingly recognized in idiopathic intracranial hypertension.
Numerous classification systems exist for encephaloceles, many of which are only of subspecialty interest, and most use very similar terminology, sometimes with different meanings . As a result reading about this topic can be frustrating. The term nasal encephalocele is, for example, variably used, often to encompass both frontoethmoidal and basal encephaloceles .
A fairly common classification still widely used is that first described by Suwanwela and Suwanwela in 1972 which divides the encephaloceles according to location :
- occipital encephalocele: ~75% of cases
- frontoethmoidal encephalocele
- interfrontal encephalocele
- associated with craniofacial clefts
- frontoethmoidal encephalocele
- parietal encephalocele
- basal encephalocele: ~10%
An encephalocele may be seen as a purely cystic mass or may contain echoes from herniated brain tissue. If the mass appears cystic, the meningocele component predominates, while a solid mass indicates predominantly an encephalocele. Larger encephaloceles may show accompanying microcephaly.
MR imaging is the best imaging modality for defining the contents of an encephalocele prior to surgery. High-resolution CT may also be used to display the bone anatomy, but the intracranial connection is best defined with MR imaging. The extent of cerebral tissue in an encephalocele is also better defined with MR imaging, which aids in prognosis and surgical planning. In some instances, focal herniation of brain parenchyma occurs into an arachnoid granulation protruding into a dural venous sinus . The cause and effect, however, is unclear and controversial.
Treatment and prognosis
The prognosis is variable depending on the presence of associated anomalies and the presence of microcephaly (carries a much poorer prognosis). A Cesarian delivery may be considered to allow for less traumatic birth for the fetal head.
- nasal encephalocoele
- otogene Meningoenzephalozele
- Chiari-Malformation Typ 3
- neuroradiology curriculum
- obstetric curriculum
- lemon sign
- fetal conditions associated with maternal diabetes
- cantrell syndrome
- congenital hydrocephalus
- juveniles Nasenrachenfibrom
- dysencephalia spanchnocystica
- intrakranielle Luft
- planum sphenoidale meningoencephalocele
- sphenoid encephalocoele
- frontoethmoidale Enzephalozele