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Resective Surgery
1
1-2
, Steven Wolf, MD .
1. Neurology Department, Beth Israel Medical Center, Albert Einstein College of Medicine, New York ,N.Y. 2. Neurological Surgery Columbia University , New York, N.Y.
Case
Epilepsy
Number Classification
Introduction
Methods
We analyzed fourteen cases of patients ages 2-49
years, thirteen of whom underwent epilepsy resective
surgery with subdural EEG monitoring. One patient
underwent bilateral strip implants for lateralization and
resective surgery is pending.
Focal
Epilepsy Etiology
Multifocal
Idiopathic
Multifocal
Vascular lesion/tumor
Focal
Focal
Focal
Focal
Vascular lesion/tumor
Focal
Focal
Vascular lesion/tumor
Focal
Focal
Vascular lesion/tumor
Focal
Focal
Static encephalopathy
Focal
Focal
Vascular lesion/tumor
Focal
Focal
Idiopathic
10
Focal
Focal
Vascular lesion/tumor
11
Focal
Focal
Idiopathic
Focal
Focal
Vascular lesion/tumor
13
Focal
Focal
Focal
Vascular lesion/tumor
Case
Surgery
Modified
Engel
outcome
TIME SINCE
SURGERY
(follow up)
IIA
2 YEARS
IIA
7.5 YEARS
IA
1.5 YEARS
IB
4.5 YEARS
IA
4.5 YEARS
Removal of tumor,
resection of anterior
temporal lobe, resection
of hipocampus and
parahippocampal
region , resection of
temporal gyrus
IA
2.5 YEARS
Frontal lobe
disconnection
IB
4 MONTHS
Resection of middle
temporal gyrus, inferior
temporal gyrus to behind
lesion to vein of Labbe
IA
5 months
IB
6 weeks
Resection of medial
temporal structures and
inferior medial and
temporal gyrus
10
IA
5 YEARS
11
Left resection
III B
6 YEARS
12
IA
2 MONTHS
13
IA
7 MONTHS
14
anterior temporal
resectionamygdalectomy
hippocampectomy
IA
2 MONTHS
12
Focal
14
Results
MFPE
EEG Findings
Table 3. Outcome
Age
Sex
Age at
seizure
17
13
17 y
2-3/week
No
since birth
15 and 21 months
4-18/day
Yes
21
since birth
19 y
4/month
Yes
21
9y
13 y
2/month
Yes
18
9.5 y
12 y
2/month - clusters
of 3-4 day
Yes
17
1.4 y
17 y
>5/day
No
17
14 y
17 y
< 1/ month
Yes
18 months
6.5 y
1 daily - 1 week
Yes
13
1y
13 y
1/week
No
10
15
since birth
10 y
3/day
Yes
11
20
10 y
13 y
3/day
No
12
31
18 y
26 and 31 y
3-4/day - 1/month
No
13
2.5
8 1/2 weeks
2y
2-3/day
Yes
14
49
42 y
49 y
2-4/month
No
Table 1. Demographics
Age at Surgery
Seizure
frequency
No. of
AEDs
Discussion
Spikes, rhythmic theta and fast beta bursts
are not the only important factors in
determining the seizure onset zone or
epileptogenic zone in epilepsy surgery.
In the analyzed cases an electrodecrement
pattern on the EEG from subdural electrode
placement aided in lateralization, localization
and definition of the epileptogenic zone
extent for surgical resection.
Electrodecrement is a useful marker to aid in
the definition of the extent of resection when
seizure onset may derive from deeper brain
structures.
Our hypothesis is that cortical areas that
show a pattern of EEG decrement are in a
pathologic hyperexitable state that make
these areas susceptible to receive
epileptiform activity originating from deep
structures (such as thalamocortical circuits)
that remain active during periods of
complete EEG flatness.
Therefore, when decrement is noted, the
epileptologist should look for a more
widespread epileptogenic zone. This, in our
experience has led to more extensive
resections and better seizure outcomes.
Bibliography
1.! Amzica, F., Basic physiology of burst-suppression. Epilepsia, 2009. 50 Suppl
12: p. 38-9.
2.! Steriade, M., F. Amzica, and D. Contreras, Cortical and thalamic cellular
correlates of electroencephalographic burst-suppression.
Electroencephalography and clinical neurophysiology, 1994. 90(1): p. 1-16.
3.! Miller, J.W. and A.J. Cole, Is it necessary to define the ictal onset zone with
EEG prior to performing resective epilepsy surgery? Epilepsy & behavior :
E&B, 2011. 20(2): p. 178-81.
4.! Janati, A., et al., Suppression-burst pattern associated with generalized
epileptiform discharges and alpha-theta pattern coma. Clinical EEG, 1986. 17
(2): p. 82-8.
5.! Ohtsuka, Y., et al., Suppression-burst patterns in intractable epilepsy with focal
cortical dysplasia. Brain & development, 2000. 22(2): p. 135-8.
6.! Lee, S.K., et al., The clinical usefulness of ictal surface EEG in neocortical
epilepsy. Epilepsia, 2000. 41(11): p. 1450-5.