TY - JOUR
T1 - How epileptogenic are temporal encephaloceles?
AU - Van Gompel, Jamie J.
AU - Miller, John W.
N1 - Publisher Copyright:
© 2015 American Academy of Neurology.
PY - 2015/10/27
Y1 - 2015/10/27
N2 - Encephaloceles are spontaneous or acquired abnormal herniations of the brain into congenital or acquired osseous-dural defects of the skull base or cranial vault. 1 When located in the middle fossa, they may present with medically intractable epilepsy, recurrent meningitis, CSF fistulas, middle ear fluid, or unilateral hearing loss. 1-3 Bony deficits may involve either the body or the greater wing of the sphenoid bone. Anteroinferior temporal encephaloceles, resulting from deficits of the horizontal portion of the greater sphenoidal wing laterally to the cranial base foramina of the sphenoidal bone, may be asymptomatic or lead to drug-resistant temporal lobe epilepsy. 1 It has long been recognized that the epilepsy associated with such encephaloceles can be surgically treated. 4,5
AB - Encephaloceles are spontaneous or acquired abnormal herniations of the brain into congenital or acquired osseous-dural defects of the skull base or cranial vault. 1 When located in the middle fossa, they may present with medically intractable epilepsy, recurrent meningitis, CSF fistulas, middle ear fluid, or unilateral hearing loss. 1-3 Bony deficits may involve either the body or the greater wing of the sphenoid bone. Anteroinferior temporal encephaloceles, resulting from deficits of the horizontal portion of the greater sphenoidal wing laterally to the cranial base foramina of the sphenoidal bone, may be asymptomatic or lead to drug-resistant temporal lobe epilepsy. 1 It has long been recognized that the epilepsy associated with such encephaloceles can be surgically treated. 4,5
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U2 - 10.1212/WNL.0000000000002073
DO - 10.1212/WNL.0000000000002073
M3 - Review article
C2 - 26408494
AN - SCOPUS:84945303816
SN - 0028-3878
VL - 85
SP - 1440
EP - 1441
JO - Neurology
JF - Neurology
IS - 17
ER -