M. Rosenow et al., HISTOPATHOLOGICAL CORRELATES OF EPILEPTOGENICITY AS EXPRESSED BY ELECTROCORTICOGRAPHIC SPIKING AND SEIZURE FREQUENCY, Epilepsia, 39(8), 1998, pp. 850-856
Purpose: To study the correlation between histopathology and epileptog
enicity, as measured by seizure frequency and electrocorticography (Ec
oG), in patients with cortical dysplasia (CD) as compared with control
patients with gangliogliomas or gliomas. Methods: The influence of th
e histopathological classification and the presence of balloon cells i
n CD on the frequency and extension of five predefined patterns of ECo
G spiking, seizure frequency, age of seizure onset and 6-month postope
rative outcome were analyzed in 32 patients with focal epilepsy underg
oing presurgical evaluation with chronically implanted subdural electr
odes. Results: Comparison of patients with CD, gangliogliomas, and gli
omas showed that the seizure frequency was greatest in patients with C
D and ECoG spiking and was most extensive in patients with ganglioglio
mas. The onset of epilepsy was earlier in patients with CD and with ga
ngliogliomas. None of these differences was significant. However, in p
atients with CD, the presence of balloon cells was associated with sig
nificantly greater seizure frequency (p = 0.009), and a significantly
greater number of electrodes recording continuous frequent spiking (p
= 0.03). The presence of continuous very frequent spiking correlated w
ith die duration of the epilepsy and the number of seizures recorded d
uring monitoring. No significant correlation was detected between hist
opathology, seizure frequency, or ECoG activity and postoperative outc
ome, which was relatively favorable in patients with balloon cells. Co
nclusions: CD refers to a variety of histopathological patterns associ
ated with different epileptogenicity. In CD, increased clinical and EC
oG epileptogenicity correlates with the presence of balloon cells. Thi
s finding confirms that balloon cells should be considered in the hist
opathological classification of CD. The predefined ECoG were not speci
fic for any of the histopathologies investigated.