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doi:10.1093/brain/awh687 Brain (2005) Page 1 of 14
Epileptogenicity of cortical dysplasia in temporallobe dual pathology: an electrophysiological studywith invasive recordings
Susanne Fauser and Andreas Schulze-Bonhage
Epilepsy Center, University of Freiburg, Freiburg, Germany
Correspondence to: Susanne Fauser, Epilepsy Center, University of Freiburg, Breisacher Strasse 64,79106 Freiburg, GermanyEmail: fauser@nz11.ukl.uni-freiburg.de
Hippocampal sclerosis is often associated with macroscopic or microscopic dysplasia in the temporal neocortex(TN). The relevance of such a dual pathology with regard to epileptogenesis is unclear. This study investigatesthe role of both pathologies in the generation of ictal and interictal activity. Ictal (113 seizures) and interictaldata from invasive EEG recordings with simultaneous depth electrodes in the hippocampus and subduralelectrodes over the TN were analysed retrospectively in 12 patients with variable degrees of hippocampalsclerosis and different types of histologically confirmed temporal cortical dysplasia [all male, age at epilepsyonset <1–29 years (mean 9.6 years), age when invasive recordings were performed 6–50 years (mean28.2 years)]. Of the seizures 41.3% arose from the amygdala/hippocampus complex (AHC), 34.7% from theTN, 22% were simultaneously recorded from AHC and TN (indeterminate seizure onset), and 2% from otherregions. In three patients, seizure onset was recorded only from the AHC. In patients with severe hippocampalsclerosis only 12% of the seizures arose from the TN, whereas in patients with mild hippocampal sclerosis 58%arose from the TN. The type of cortical dysplasia, however, did not predict seizure onset in the AHC or TN.Propagation time from the TN to the AHC tended to be shorter (mean 7.4 s) than vice versa (mean 13.7 s). Themost common initial ictal patterns in the AHC were rhythmic beta activity (<25 Hz) and repetitive sharp waves,and in the TN were fast activity (>25 Hz) and repetitive sharp waves. The interictal patterns over the TN weresimilar to those seen over extratemporal focal cortical dysplasias. Simultaneous recordings from the hippo-campus and the TN strongly suggest that dysplastic tissue in the TN is often epileptogenic. The quantitativecontribution of the hippocampus to seizure generation corresponded with the degree of hippocampal patho-logy, whereas different subtypes of cortical dysplasia did not affect its relative contribution to seizure generationand even mild forms of dysplasia were epileptogenic.
Keywords: hippocampal sclerosis; focal cortical dysplasia; invasive EEG recording; epileptogenesis
Abbreviations: AHC = amygdala/hippocampus complex; FCD = focal cortical dysplasia; mMCD = mild malformations of corticaldevelopment; MTD = mild mesial temporal damage; non-REM = non-rapid eye movement; TN = temporal neocortex
Received April 18, 2005. Revised July 11, 2005. Accepted October 7, 2005
IntroductionAn association of hippocampal sclerosis with macroscopic or
microscopic cortical dysplasia in the temporal lobe has
recently been discovered as a quite common pathology and
has come into the focus of interest. Histologically, dysplastic
features such as columnar and laminar disorganization, clus-
ters of disorganized and misshaped neurons and rarely also
balloon cells are found in the neocortical temporal cortex
in 10–50% of patients with hippocampal sclerosis (Prayson
et al., 1996; Kasper et al., 2003; Diehl et al., 2004; Kalnins
et al., 2004).
Although this dual pathology of the temporal lobe is fre-
quently observed in epilepsy patients, the clinical significance
of the dysplastic tissue in the neocortical temporal lobe, in
particular its epileptogenesis, remains unclear (Reynolds,
1987; Raymond et al., 1994; Holmes et al., 1998; Huang
et al., 1999; Thom et al., 2001). Reports on the post-operative
outcome of these patients are controversial. Early studies
reported that patients with hippocampal sclerosis and asso-
ciated microscopic cortical dysplasia have a higher risk for
seizure recurrences after epilepsy surgery (Engel, 1992;
# The Author (2005). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org
Brain Advance Access published November 29, 2005
Palmini et al., 1994) as compared with patients with mesial
temporal sclerosis only. More recent investigations, however,
could demonstrate that these patients can have a very favour-
able outcome provided that both pathologies were removed
(Thom et al., 2001; Srikijvilaikul et al., 2003; Fauser et al.,
2004; Kalnins et al., 2004). Post-surgical outcome data alone
leave open questions regarding the relative contribution of
both pathologies to ictogenesis. Simultaneous invasive record-
ings from both the hippocampus and the temporal neocortex
(TN) may provide additional information on this topic and
thus contribute to a better understanding of the clinical sig-
nificance of such dysplastic tissue in the neocortical temporal
lobe. Electroclinical data of invasive EEG recordings in
patients with hippocampal sclerosis associated with micro-
scopic cortical dysplasia of the temporal lobe have not been
reported until now.
In the present study we analysed ictal (113 seizures) and
interictal data in 12 patients with variable degrees of hippo-
campal sclerosis associated with different types of cortical
dysplasia in the temporal lobe who underwent invasive
video EEG recordings. All of them were simultaneously
implanted with subdural strip electrodes or grid electrodes
over neocortical areas (temporo-lateral/-basal) and depth
electrodes in the amygdala/hippocampus complex (AHC).
Patients and methodsA total of 12 patients with pharmacoresistent epilepsy were
included in the study, 11 of them with histologically confirmed
dual pathology of the temporal lobe and 1 additional patient with
histologically confirmed hippocampal sclerosis and typical MRI fea-
tures of transmantle dysplasia. In all of them, invasive video EEG
monitoring was performed simultaneously with subdural electrodes
over the TN and depth electrodes in the AHC (see Presurgical evalu-
ation) between May 1998 and October 2004. The data were analysed
retrospectively.
Demographical dataAll investigated patients were of male gender. The age at epilepsy
onset ranged from <1 to 29 years (mean 9.6 years, median 8 years),
and the age when invasive recordings were performed ranged from
6 to 50 years (mean 28.2 years, median 33 years).
Presurgical evaluationPresurgical evaluation was performed in the Epilepsy Center at the
University hospital of Freiburg, Germany. All patients underwent
presurgical MRI. MRI scans were acquired with a 1.5 T scanner
(Siemens magnetom Vision or Siemens Magnetom Symphony,
Erlangen, Germany). The following sequences were performed:
T1-weighted images with and without gadolinium-DTPA, T2-
weighted images, fluid-attenuated inversion recovery images and
magnetization-prepared rapid gradient echo sequences. Addition-
ally, axial images were acquired with a modified angulation parallel
to the long axis of the temporal lobe to evaluate the mesio-temporal
structures. MRI criteria suggestive for focal cortical dysplasia were
gyration anomalies, focal thickenings of the cortex, blurring of the
grey–white matter junction, and abnormal cortical and subcortical
signal intensity.
Invasive video EEG monitoring was indicated because patients
were cryptogenic in the MRI (2 patients), had an additional lesion in
the frontal lobe (2 patients), had cortical dysplasia temporo-poster-
ior in the dominant hemisphere (1 patients), had a frontal semiology
with hypermotor seizures and a wide fronto-temporal field of seizure
onset on scalp EEG (3 patients), had a parieto-occipital or temporo-
posterior seizure onset on scalp EEG (2 patients), had a bilateral
seizure onset (1 patient) or because a very circumscribed resection
was aimed at (1 patient).
Multicontact depth electrodes (Ad-tech�, Racine, WI) were
inserted into the hippocampus from a posterior approach in all
12 patients. Depth electrode recordings were performed with 10
contacts in 10 patients and with 5 contacts in 2 patients. Two to
four temporo-basal subdural strip electrodes and one to four
temporo-lateral subdural strip electrodes were inserted in all 12
patients. Temporo-lateral double-strip electrodes (6 patients) or
grid electrodes (2 patients) overlying also temporo-posterior, occi-
pital or parietal areas were used when seizure onset was suspected
outside the temporal lobe. Additional fronto-basal (3 patients),
fronto-lateral (3 patients) or interhemispheric subdural strip
electrodes (2 patients) were used in patients with frontal semiology
or an additional frontal lesion. Mean total number of recording sites
was 58.5.
EEG recordings and analysisEEG data acquisition was performed with a Neurofile NT digital
video EEG system (It-med, Usingen, Germany), with 128 channels,
256 Hz sampling rate and a 16 bit analogue-to-digital converter. Data
were band pass filtered between 0.53 and 80 Hz.
EEG-analyses were performed by two board-certified electro-
encephalographers. Mean video EEG recording period was 7 days
(range 2–13 days). In each patient, the first 10 recorded seizures were
analysed. In 4 patients, in whom <10 seizures were recorded, all
available seizures (n = 7–9 seizures, see Table 1) were considered.
Complex partial seizures, simple partial seizures and subclinical seiz-
ure patterns were included. The ictal pattern was analysed in the area
of seizure onset and in the area of the second lesion after propaga-
tion (e.g. the AHC in seizures arising from the dysplastic TN or the
dysplastic TN in seizures arising from the AHC). Ictal patterns were
classified as rhythmic spikes/sharp waves, rhythmic a activity, rhyth-
mic b activity, rhythmic u activity, rhythmic d activity, fast activity
(>25 Hz) including low amplitude fast activity (lafa) and depression
in amplitude. In our analysis, we have classified electrographic pat-
terns as subclinical ictal patterns if such patterns showed evolution in
frequency and/or topography (in contrast to the interictal patterns
without evolution shown in Fig. 1). Subclinical ictal patterns
included in the analysis occurred after the initial day of placement
of intracranial electrodes. Exclusion of subclinical seizures (n = 13)
did not significantly change the overall results.
Additionally, interictal activity was investigated in the TN. Inter-
ictal activity was classified as isolated spikes, repetitive spike pattern,
paroxysmal fast pattern and slow repetitive spike pattern
(Boonyapisit et al., 2003) (Fig. 1). Interictal patterns were analysed
during wakefulness and during non-rapid eye movement (non-
REM) and REM sleep. As additional recordings with scalp electrodes
were not available for the whole recording period and the first 10
seizures were considered, an analogous correlation of ictal data to
wakefulness and sleep was not performed.
Page 2 of 14 Brain (2005) S. Fauser and A. Schulze-Bonhage
Table 1 Summary of MRI diagnosis, histology, areas of seizure onset and propagation time in patients with dual pathology
Patient no. MRI diagnosis Histology Number ofevaluated seizures
Seizure onset Propagation time
1 Cryptogenic FCD 1b, HS Wyler 1 10 TN: 5 TN-> AHC: 1.2 sAHC: 0ID: 3CL: 2
2 FCD left temporal FCD 2b, HS Wyler 1 10 TN: 9 TN -> AHC: 11.4 sAHC: 1 AHC -> TN: 1.0 sID: 0CL: 0
3 FCD temporo-polar, insular,mesiofrontal left, HS left
FCD 1b, HS Wyler 3 10 TN: 0 AHC -> TN: 2.8 sAHC: 10ID: 0CL: 0
4 FCD occipito-temporal andfrontoparasagittal, HS right
HS Wyler 3 10 TN: 0 AHC -> TN: 1.5 sAHC: 10ID: 0CL: 0
5 Very discrete FCD temporo-polar,discrete HS left
FCD 1b, HS Wyler 1 9 TN: 7* TN -> AHC: 6.0 sAHC: 1 AHC -> TN: 2.0 sID: 1CL: 0
6 FCD temporo-polar, HS right FCD 1b, HS Wyler 3 7 TN: 0 AHC-> TN: 33.4 sAHC: 5ID: 2CL: 0
7 FCD temporo-polar, HS right FCD 1a, HS Wyler 3 10 TN: 6* TN -> AHC: 14.0 sAHC: 2*ID: 2CL: 0
8 FCD temporo- polar, HS right FCD 1b, HS Wyler 3 10 TN: 0 AHC -> TN: 34.4 sAHC: 10ID: 0CL: 0
9 Cryptogenic FCD 1b, HS Wyler 1 10 TN: 0AHC: 0ID: 10CL: 0
10 HS right mMCD, HS Wyler 3 8 Undecided
11 FCD temporo-occipitalbilaterally
FCD 1b, HS Wyler 1 7 TN: 1AHC: 3ID: 2CL: 3
12 FCD right parahippocampal gyrus mMCD, HS Wyler 1 10 TN: 7 TN -> AHC: 4.4 sAHC: 0ID: 3CL: 0
FCD; focal cortical dysplasia (for classification according to Palmini see section Neuropathological examination, page 4), mMCD; mildmalformation of the cortical development, HS; hippocampal sclerosis (for classification according to Wyler see section Neuropathologicalexaminations, page 4), AHC; amygdala/hippocampus complex, ID; indeterminate onset (simultaneously recorded in TN and AHC), CL;contralateral to the operated site, TN; dysplastic temporal neocortex; *These numbers include subclinical seizure patterns. Patient 5: TN:seven seizures were all subclinical seizure patterns. Patient 7: TN: six seizures included two clinically manifested seizures and four subclinicalseizure patterns with identical seizure onset pattern. AHC: two seizures were both subclinical seizures.
Hippocampal sclerosis and cortical dysplasia Brain (2005) Page 3 of 14
Surgical proceduresEpilepsy surgery was tailored according to the ictal and interictal
results of invasive EEG recordings. Interictal activity was considered,
as former studies could show that the extent of interictal epileptiform
activity may be a more accurate estimate of the epileptogenic region
compared with either the seizure onset region or the pathologic
substrate (Bautista et al., 1999). In four patients an anterior temporal
lobe resection including an amygdalohippocampectomy was
performed, and five patients underwent an anterior temporal lobe
resection with posterior extension including amygdalohippocampec-
tomy. In two patients an extended temporal pole resection including
amygdalohippocampectomy and in one patient a selective amydalo-
hippocampectomy were performed.
In four patients (nos 1, 2, 9 and 12) with predominantly or only
TN seizure onset an amygdalohippocampectomy was recommended
because of the fast spread of ictal activity into the AHC (<2 s) or the
immediate involvement of both structures (indeterminate seizure
onset) (Table 1). In these cases we considered the AHC as having
a reduced seizure threshold and as a possible part of the epileptogenic
region. Patients were informed about the risk of post-operative
memory impairment and the patients gave their consent.
Neuropathological examinationsAfter excision, the tissue was fixed for 12–24 h in 10% buffered
formalin, embedded in paraffin and sectioned. Staining was carried
out using haematoxylin–eosin, periodic acid-Schiff and Kluever–
Barrera myelin stain. For selected cases, additional special stains
(Elastica-van-Gieson, Reticulin, Bodian) were used. Additional
immunohistochemical stainings were performed with antibodies
Fig. 1 (A–D) Interictal patterns which were observed over the dysplastic TN during wakefulness and sleep.
Page 4 of 14 Brain (2005) S. Fauser and A. Schulze-Bonhage
against neurofilament to visualize the orientation of neurons and to
depict dysmorphic neurons or ectopic white matter neurons and
against synaptophysin, another neuronal marker. Glial fibrillary
acid protein (GFAP) and vimentin immunohistochemistry was per-
formed in order to better visualize astrogliosis and/or balloon cells.
Moreover, the proliferation marker Ki-67, the pan-leucocyte marker
leucocyte common antigen and the microglial marker CD68 were
applied.
Histological dysplastic features were classified as suggested by
Palmini and Luders (2002).
Dyslamination was the inclusion criterion for the diagnosis of
focal cortical dysplasia (FCD) type 1: FCD 1a was defined as a blurred
transition between different cortical layers, in our patient group most
commonly seen between layers III and IV or layers V and VI. In these
zones we observed a relatively homogenous population of neurons
and a moderately increased cell density. Occasionally, dyslamination
was characterized by a numerical reduction of pyramidal neurons
and granule cells and clusters of misplaced neurons (e.g. an increased
number of pyramidal neurons in layers I or II with abundant ectopic
neurons in the white matter). FCD 1b was diagnosed if the laminar
disorganization was more prominent and occurred together with
cytoarchitectural abnormalities such as immature neurons (a popu-
lation of neurons with a large nucleus and a thin rim of cytoplasma)
and/or giant neurons.
Abundant heterotopic white matter neurons in the absence of a
dyslamination were described as mild malformations of cortical
development (mMCD).
Dysplastic tissue with the additional occurrence of dysmorphic
neurons was classified as FCD 2a, and dysplastic tissue with the
additional occurrence of balloon cells as FCD 2b.
The histological grading of hippocampal pathology was classified
according to Wyler et al. (1995). Grade 1: mild mesial temporal
damage (MTD) with gliosis and <10% or no hippocampal neuronal
dropout involving sectors CA1, CA3 and/or CA4 of hippocampal
pyramidal cell layer. Grade 2: moderate MTD with gliosis and
10–50% neuronal dropout involving sectors CA1, CA3 and/or
CA4 of hippocampal pyramidal cell layer. Grade 3: moderate to
marked MTD with gliosis and >50% neuronal dropout involving
sectors CA1, CA3 CA4 of hippocampal pyramidal cell layer but
sparing CA2. Grade 4: marked MTD with gliosis and >50% neuronal
dropout involving all sectors of hippocampal pyramidal cell layer.
Statistical analysisFor comparison of propagation times in seizures arising from the
hippocampus and seizures arising in the dysplasia the two-tailed
t-test was used. For comparison of the location of seizure onset in
patients with severe and mild hippocampal sclerosis the chi-square
test was used. P-values <0.05 were regarded as statistically significant.
ResultsHistology, MRI and outcomeHistological and MRI findings are summarized in Table 1. Of
the 12 patients six showed mild hippocampal sclerosis
(Wyler 1) and six showed severe hippocampal sclerosis
(Wyler 3). In the neocortical temporal lobe, in two patients
abundant white matter neurons were the only histological
dysplastic feature (mMCD), and in one patient FCD 1a, in
seven patients FCD 1b and in one patient FCD 2b were seen.
In one further patient the area showing MR features of cortical
dysplasia was not removed as invasive recordings did not
show ictogenesis arising from this area. In this patient, how-
ever, the MRI findings were highly suggestive for FCD 2b in
temporo-posterior localization.
In 6 out of 12 patients the FCD and the hippocampal
sclerosis were visible in MRI. In 3 out of 12 patients only
the FCD and in 1 patient only hippocampal sclerosis was
detectable in MRI. Of the 12 patients 2 had no imaging
abnormalities. Sensitivity of MR scanning for correct detec-
tion of hippocampal sclerosis was higher when more severe
forms of neuronal damage were present.
Post-surgical outcome was favourable in most cases.
Post-surgical outcome was classified according to Engel
and Rasmussen (1993) and was related to the latest follow-up
visit (range 6–36 months, mean 18 months). Of all the
patients, seven were completely seizure free (Engel Ia), two
had only simple partial seizures or a running down of
seizure frequency with complete seizure freedom over 2
years (Engel Ib and Engel Ic), one patient had >90% seizure
reduction (Engel II), one patient with contralateral seizure
onset had considerable reduction of seizure frequency
(�75%) (Engel III), and one patient with both neocortical
and hippocampal seizure onset did not benefit from epilepsy
surgery (Engel IV). Patients with severe hippocampal sclerosis
were all Engel I (three patients Engel Ia, one patient Engel
Ib and Ic each). In the patient group with mild hippocampal
sclerosis three patients were Engel Ia, and one patient Engel II,
III and IV each.
Ictal onset zones and spreadA total of 96 seizures from 10 patients were quantitatively
evaluated, and 17 seizures in 2 additional patients (nos 10
and 11) are described separately.
Of the evaluated seizures 41.3% arose from the AHC
(Fig. 2A and B) and 34.7% from the dysplastic TN
(Fig. 2C). In 22% of the evaluated seizures, seizure onset
was indeterminate as it was simultaneously recorded over
both areas, the AHC and the TN (Fig. 2D). In these seizures,
larger networks were obviously very early activated. Although
seizure semiology did not differ between seizures with definite
hippocampal or extrahippocampal onset as compared with
seizures with indeterminate onset in the same patient, an
analysis of the time lag between electrographic seizure
onset and initial behavioural signs or symptoms showed
that in two patients (nos 6 and 7) seizures with initial elec-
trographic patterns in both regions had a more rapid onset of
clinical manifestations. Of the evaluated seizures 2.0% arose
from the contralateral hemisphere.
Of the seizures arising from the AHC 70% propagated
into the dysplastic TN and of the seizures arising from the
dysplastic TN 72.4% propagated into the AHC. On patient
level, in three patients all evaluated seizures arose only from
the AHC. In the other patients, seizures arose in various
combinations from the AHC and/or the TN and/or were
simultaneously recorded over both areas (indeterminate
Hippocampal sclerosis and cortical dysplasia Brain (2005) Page 5 of 14
seizure onset). Only one of the five patients with Wyler 3
pathology had independent TN seizure onset (Table 1).
Seizure onset from the AHC was significantly more fre-
quent in patients with severe hippocampal sclerosis than in
patients with mild hippocampal sclerosis (P < 0.0001), and
seizure onset from the TN was significantly more common in
patients with mild hippocampal sclerosis (P < 0.0001). In five
patients with severe hippocampal sclerosis (Wyler 3), 78% of
the evaluated seizures arose from the AHC only, 10% had
indeterminate seizure onset and 12% arose from the
dysplastic TN only. In the five patients with mild hippocam-
pal sclerosis (Wyler 1) 4% of the evaluated seizures arose from
the AHC, 34% had indeterminate seizure onset and 58% arose
from the dysplastic TN (Fig. 3).
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Page 6 of 14 Brain (2005) S. Fauser and A. Schulze-Bonhage
Regarding the types of focal cortical dysplasia, seizure
origin was highly variable. In two patients with severe FCD
2b, seizure onset was nearly complementary. In one of them
(no. 2) 90% of the seizures arose from the dysplastic TN and
10% from the hippocampus. In the other patient (no. 4),
100% of the evaluated seizures arose from the hippocampus.
In eight patients with mild dysplastic features in the TN (clas-
sified as mMCD, FCD 1a and FCD 1b) seizure onset zones
varied considerably. In four of them, none of the seizures arose
from the dysplastic TN alone, 32.2% had indeterminate seiz-
ure onset and 67.5% of the seizures arose from the AHC. In the
other four patients (including one patient with mMCD), the
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Hippocampal sclerosis and cortical dysplasia Brain (2005) Page 7 of 14
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Fig. 2 (A) Example of seizure onset (arrow) with rhythmic sharp waves in the amygdala and anterior hippocampus. (B) Example of seizureonset (arrow) with rhythmic beta activity in the amygdala and anterior hippocampus. (C) Example of a seizure from Patient 1: seizure onset(first arrow) is seen with a fast activity in the temporo-basal neocortex, temporo-anterior lateral neocortex and enthorhinal cortex. After1 s (second arrow) the seizure has propagated in the AHC in which a rhythmic beta activity appears. Immediately before seizure onsetrhythmic spikes are seen over the temporo-basal neocortex, temporo-anterior lateral neocortex and enthorhinal cortex, which werefrequently observed interictally. (D) Example of seizure onset (arrow) with fast activity, the onset of which is simultaneously recorded overneocortical and mesial temporal areas (indeterminate seizure onset). (E) Example of a seizure from Patient 7 showing interaction betweenneocortical and hippocampal regions in seizure generation. In this example seizure onset is seen with a beta activity in the temporo-basaland tempror-anterior lateral neocortex (first arrow). Simultaneously with seizure onset there is a decrement of the amplitudes in thehippocampal depth electrode. One second before the seizure activity is seen in the hippocampus, the temporo-basal and temporo-lateralbeta activity disappears (second arrow). With the onset of the rhythmic beta activity in the hippocampal electrode contacts (third arrow),low amplitude fast activity is recorded over the temporo-basal neocortex. (F) Example of a seizure from Patient 10. In this patient anelectrographic status epilepticus limited to the intrahippocampal electrode contacts (panel 1) was observed during the complete period ofvideo EEG monitoring. This rhythmic spiking showed repeated transition into other ictal patterns every 10 min (panel 2). Infrequently lowamplitude fast activity (arrow) was recorded from the temporo-basal cortex resulting in a clinical seizure (panel 3). In this case, it wasimpossible to decide whether this low amplitude fast activity was related to the preceding ictal pattern in the hippocampus.
Page 8 of 14 Brain (2005) S. Fauser and A. Schulze-Bonhage
majority of seizures (64.5%) were generated in the dysplastic
TN, 23.5% had indeterminate seizure onset and only 8.5%
arose from the AHC alone.
Two of the patients (nos 10 and 11) were not included in
the quantitative evaluation.
In the first patient (Fig. 2F), EEG long-term recording
revealed electrographic status epilepticus consisting of
continuous 1/s rhythmic sharp wave activity limited to
only the third electrode contact of the depth electrode in
the anterior hippocampus during the complete 8 day period
of invasive EEG monitoring and this could not be recorded
by in the closeby subdural electrode contacts. This rhythmic
spiking showed repeated transitions into subclinical ictal
patterns and a waxing and waning spatial distribution
every 10–20 min. In addition, infrequently low amplitude
fast activity was recorded from the anterior temporo-basal
cortex, resulting in a clinically manifested complex partial
seizure. It was impossible to decide whether this low ampli-
tude fast activity was related to the ongoing ictal pattern in the
hippocampus (Fauser and Schulze-Bonhage, 2004); thus, a
classification as for the other patients could not be used.
In the second patient (patient no. 11) MRI revealed a bilat-
eral cortical dysplasia in temporo-occipital localization. The
left temporal lobe was resected because the majority of sei-
zures were arising from that area: one seizure from the TN,
three from the AHC and two with indeterminate seizure
onset. Three seizures, however, were arising from the right
temporal lobe: one from the TN and two with indeterminate
seizure onset.
Propagation times from the dysplasticTN into the AHC and vice versaPropagation times were separately determined in seizures
arising from the AHC with propagation into the dysplastic
TN and in seizures arising from the dysplastic TN with pro-
pagation into the AHC. In our patient sample, there was no
significant difference between AHC to TN versus TN to AHC
propagation times (P = 0.5); however, the former tended to be
longer than the latter. In seizures arising from the dysplastic
TN, propagation time ranged from 1 to 26 s, and the mean
propagation time was 7.4 s. In seizures arising from the AHC,
propagation time ranged from 1 to 76 s, and the mean pro-
pagation time was 13.7 s.
Initial ictal patternsThe initial ictal patterns in patients with dual pathology are
shown in Figs 2 and 4. In seizures arising from the dysplastic
TN (Fig. 4A), fast activity (>25 Hz) (50.5%) and repetitive
sharp waves (35.6%) were the most common initial patterns.
In the secondarily involved AHC (Fig. 4B) rhythmic beta
activity (36.2%) was the most common pattern (Fig. 2C).
Fast activity (>25 Hz), however, was rarely observed (7.3%).
In seizures arising from the AHC (Fig. 4C) rhythmic beta
activity (<25 Hz) (47.1%) and rhythmic sharp waves (28.6%)
(Fig. 2A) were the most common initial ictal patterns. Fast
activity (>25%) was only seen in 4.2% of the evaluated sei-
zures. In the secondarily involved dysplastic TN (Fig. 4D) fast
activity (40.5%) was the most common pattern followed by
rhythmic sharp waves (38.3%).
In seizures with indeterminate onset fast activity (>25 Hz)
was the most common initial ictal pattern in the dysplastic TN
(91.7%). In the AHC fast activity and rhythmic beta activity
were both seen in 27.8% of seizures (Fig. 4E and F).
Few seizures were not included in the quantitative analysis
as it was uncertain whether the ictal pattern seen in the AHC
was related to the preceding ictal pattern in the dysplastic TN
(Fig. 2E) or vice versa (Fig. 2F).
Interictal patterns in the temporalneocortexInterictal patterns (Fig. 1) were evaluated during wakefulness,
non-REM sleep and REM sleep in the electrode contacts over-
lying the dysplastic TN. The results are summarized in Table 2.
Isolated spikes, a repetitive spike pattern (intermittent or
almost continuous), and a paroxysmal fast pattern were fre-
quently seen during wakefulness and non-REM sleep. A repet-
itive bursting pattern, however, was only seen in one patient
during non-REM sleep. In this patient a FCD 2b (Taylor type)
was diagnosed.
Localization of repetitive spike pattern, low amplitude fast
activity and repetitive bursting pattern in the TN is shown in
Table 3 and compared with the seizure onset zone. In most
cases there was an overlap between both the zone of seizure
onset and the zone of interictal patterns. However, in general,
the interictal zone was more extended.
DiscussionThe clinical significance of microscopic cortical dysplasia in
the TN found in 10–50% of patients with hippocampal scler-
osis is an issue of intense debate. In the present study 113
seizures in 12 patients with dual pathology of the temporal
lobe who underwent invasive video EEG monitoring were
investigated. Though patient numbers were limited in our
study several conclusions may be drawn from our data.
0%
10%
20%
30%
40%
50%
60%
70%
80%
90%
100%
mild hippocampal sclerosis severe hippocampal
sclerosis
AHC
ID
TN
0%
10%
20%
30%
40%
50%
60%
70%
80%
90%
100%
mild hippocampal sclerosis severe hippocampal
sclerosis
AHC
ID
TN
Fig. 3 Distribution of seizure onset zones in patients with mildand severe hippocampal sclerosis.
Hippocampal sclerosis and cortical dysplasia Brain (2005) Page 9 of 14
A:
C:
E:
B:
D:
F:
Fig. 4 (A and B) Occurrence of different initial ictal patterns in the dysplastic TN and ictal patterns observed in the secondarily involvedAHC in seizures arising in the TN. (C and D) Occurrence of different initial ictal patterns in the AHC and ictal patterns observed in thesecondarily involved dysplastic TN in seizures arising in the amygdala/hippocampus complex. (E and F ) Occurrence of different initial ictalpatterns in the AHC and the dysplastic TN in seizures with indeterminate onset.
Page 10 of 14 Brain (2005) S. Fauser and A. Schulze-Bonhage
The quantitative contribution of the AHCto seizure generation seems to correlatestrongly with degree of hippocampalpathology whereas a relation with differenttypes of cortical dysplasia in the temporalneocortex was not evidentSeizure onset from the AHC was significantly more frequent
in patients with severe hippocampal sclerosis than in patients
with mild hippocampal sclerosis (P < 0.0001). Seizure onset
from the TN, however, was significantly more frequent in
patients with mild hippocampal sclerosis (P < 0.0001). In
contrast, the type of cortical dysplasia alone did not predict
a temporo-neocortical or temporo-mesial seizure onset in our
patient group. Any type of cortical dysplasia could be epilep-
togenic or could be electrically inert; for example, two patients
with severe cortical dysplasia (FCD 2b) (histologically
confirmed or suspected by MRI findings) behaved nearly
complementarily, with preponderance of hippocampal seiz-
ure onset in one and preponderance of seizure onset in the TN
in the other. The fact that areas of severe cortical dysplasia can
be electrically inert is known from patients with tuberous
sclerosis, in whom a leading tuber can frequently be identi-
fied whereas most of the additional tubers seem not to be
epileptogenic. Similarly in patients with mild histological dys-
plastic features (classified as MCD, FCD 1a or 1b) the per-
centage of seizure onset from the dysplastic TN was highly
variable and ranged from 0 to 78% per patient.
A preponderance of hippocampal seizure onset is not
unusual in other multifocal epilepsies with hippocampal
sclerosis (i.e. after viral encephalitis or traumatic brain injury)
and does not exclude an additional extrahippocampal seizure
onset zone. In this context, one study (Li et al., 1999)
could demonstrate that in a group of patients with
Table 2 Interictal patterns in the dysplastic TN
Awake Non-REM REM
Isolated spikes 12/12 patients (100%) 12/12 patients (100%) 7/9 patients (78%)Repetitive spike pattern 8/12 patients (67%) 9/12 patients (75%) 4/9 patients (44%)Paroxysmal fast pattern 5/12 patients (42%) 6/12 patients (50%) 3/9 patients (33%)Repetitive bursting pattern 0/12 patients (0%) 1/12 patients (8%) 0/9 patients (0%)
Table 3 Localization of seizure onset and interictal patterns in the dysplastic TN
Patient no. Seizure onset zone Interictal pattern and respective localization
1 Temporo-anterior, mid-temporal(basal + lateral)
Repetitive spike pattern: temporo-anterior (basal + lateral)Paroxysmal fast pattern: temporo-anterior,mid-temporal (lateral)
2 Temporo-anterior, mid-temporal,tempror-posterior (basal and lateral)
Repetitive spike pattern: temporo-anterior, mid-temporal,temporo-posterior (lateral)Paroxysmal fast pattern: temporo-anterior (lateral + basal), mid-temporal (lateral)Repetitive bursting pattern: temporo-posterior (basal)
3 – Repetitive spike pattern: mid-temporal (lateral), occipital (basal)Paroxysmal fast pattern: temporo-anterior (lateral),mid-temporal (basal), frontal (lateral), occipital (basal)
4 – –5 Temporo-anterior (lateral),
temporo-posterior (basal)Repetitive spike pattern: temporo-anterior (lateral + basal),mid-temporal, temporo-posterior (basal)
6 Temporo-anterior (basal) Repetitive spike pattern: temporo-anterior,mid-temporal (lateral), temporo-posterior (basal), frontal (basal)
7 Temporo-anterior (basal) Repetitive spike pattern: temporo-anterior,mid-temporal (lateral + basal)Paroxysmal fast pattern: mid-temporal, temporo-posterior (lateral)
8 – Repetitive spike pattern: temporo-posterior (lateral + basal),frontal (basal)
9 Temporo-anterior (lateral + basal) Repetitive spike pattern: temporo-anterior (lateral + basal)10 Temporo-anterior (basal) Repetitive spike pattern: temporo-anterior (basal),
mid-temporal (lateral)Paroxysmal fast pattern: temporo-anterior,mid-temporal, temporo-posterior (basal), mid-temporal lateral
11 Mid-temporal, temporo-posterior (left),mid-temporal (lateral) (right)
Repetitive spike pattern: frontal left, temporo-parietal left (lateral)
12 Mid-temporal (lateral),temporo-posterior (basal)
Repetitive spike pattern: temporo-anterior (lateral)mid-temporal (basal and lateral)Paroxysmal fast pattern: temporo-anterior (lateral), mid-temporal, temporo-posterior(basal)
Hippocampal sclerosis and cortical dysplasia Brain (2005) Page 11 of 14
extrahippocampal lesions (including cortical dysgenesis,
tumours, contusions, infarcts and vascular malformations)
associated with hippocampal atrophy, even if the atrophied
hippocampus appeared to be the most epileptogenic struc-
ture, only 20% of the patients became seizure free after hip-
pocampal removal. In our patient group with severe
hippocampal sclerosis, however, all patients had a very
favourable seizure outcome (Engel class I) after removal of
the hippocampus and the neocortical areas of seizure onset
and/or with severe interictal activity.
Although patients with severe and mildhippocampal sclerosis differ in the relativecontribution of the AHC and the TN toseizure onset, there is an overlap betweenboth groupsEven in our small patient group, we observed one patient with
severe hippocampal sclerosis in whom the majority of seizures
arose from the TN. Thus, in patients with severe hippocampal
sclerosis and a dysplastic TN, seizure onset from the TN seems
not to be an exception and is probably more common than in
patients with mesial temporal sclerosis alone, in which seizure
onset from the TN is reported in only 0–5% in most studies
(Lieb et al., 1976; Delgado-Escueta and Walsh, 1983; Quesney,
1986; Morris et al., 1987; Maldonado et al., 1988; Sperling and
O’Connor, 1989; So et al., 1989; Spencer et al., 1990; King and
Spencer, 1995). These data, however, may be influenced by the
preselection of patients for invasive EEG recordings; factors
favouring an additional invasive EEG recording included
seizure semiology, scalp EEG or MRI findings not typical
for only temporo-mesial seizure onset. In patients with
mild hippocampal sclerosis, the hippocampus played a less
important role in the ictogenesis. However, 2 patients with
mild hippocampal sclerosis were observed in whom one of the
first 10 seizures arose from the AHC. The relative contribu-
tion of the AHC and the TN to ictogenesis in this patient
group resembles reported percentages on patients with tem-
poral lobe epilepsy and no or mild hippocampal sclerosis
(35% temporal extrahippocampal, 24% regional, 29% lobar
and 3% hippocampal) (Vossler et al., 2004). In that study,
however, no dysplastic features were observed in the removed
TN and the aetiology of epilepsy remained unclear.
From these data we conclude that patients with dual patho-
logy of the temporal lobe constitute a broad spectrum as far
as ictal onset zones are concerned, and that even mild forms
of cortical dysplasia and hippocampal sclerosis can generate
seizures.
Propagation time of ictal activity tends tobe shorter in seizures arising in thedysplastic temporal neocortex than inseizures arising in the hippocampusStudies on propagation time of ictal activity from the TN into
the hippocampus and vice versa are rare. One former study in
patients with temporo-neocortical and temporo-mesial seiz-
ure onset (Brekelsmans et al., 1995) reported a propagation
time of 17.3 s from the neocortex into the limbic region and of
34.9 s from the limbic region into the neocortex. The aetiology
of temporo-lateral seizure onset is not mentioned. Compared
with that study, in our patient group with dual pathology of
the temporal lobe propagation time of ictal activity from the
temporo-mesial structures to the TN (13.7 s) and from the
TN to the temporo-mesial structures (7.4 s) was shorter but
showed a similar trend, however, without statistical signific-
ance. Additional factors such as different anticonvulsive drug
regimes may contribute to these differences.
Initial ictal patterns differ between theAHC and the dysplastic TNComparing seizure onset patterns in the TN to seizure onset
patterns in the AHC, in our patient group in accordance with
earlier reports (Javidan, 1992), seizure onset patterns in the
TN were characterized by higher frequency than in the AHC:
In the dysplastic TN, fast activity (>25 Hz) was the most
commonly observed pattern, independently from the fact
whether seizures were arising from this region or propagating
into this region. Thus, also fast activity over the TN did not
give any guarantee that the area displaying it is the initial
seizure onset zone. In the temporo-mesial structures, rhyth-
mic beta activity was the most common pattern, which was
also independent from the fact whether seizures were arising
from or propagating into the temporo-mesial structures. Fast
activity, however, was very rarely observed in the AHC. More
suggestive for a spread from another site into the temporo-
mesial structures was a combination of different patterns
within the temporo-mesial structures or an initial flattening
of amplitudes.
The analysis shows that EEG patterns depended more on
the structure where seizures arise from as compared with the
exact point-of-onset. These dependencies may also be reflec-
ted in the scalp EEG (Ebersole and Pacia, 1996). However,
all scalp EEG patterns are secondary to involvement of the
temporo-lateral convexity and thus do not directly reflect the
mesio-temporal seizure onset patterns investigated here.
Interictal patterns in FCD of the temporallobe associated with hippocampal sclerosisresemble interictal patterns in FCD ofextratemporal lobes but are lessfrequently observedIn our study, interictal patterns were evaluated during wake-
fulness and sleep (non-REM and REM sleep). A repetitive
spiking pattern was seen in 75% of patients; however, only
in three of them (25%) it was observed continuously or
quasicontinuously. A repetitive bursting pattern was seen
in only 1 patient (8.3%) with FCD type 2b (Taylor type)
containing balloon cells and dysmorphic neurons. A former
study in patients with FCD in extratemporal localization
Page 12 of 14 Brain (2005) S. Fauser and A. Schulze-Bonhage
(Palmini et al., 1995) reported 35% of the patients with con-
tinuous or quasicontinuous rhythmic spiking and 30% of the
patients with a repetitive bursting pattern. In that group, most
of the patients had FCD type 2b (Taylor type) in the histo-
logical examination. Similarly, another study (Boonyapisit
et al., 2003) correlated interictal patterns to the underlying
pathological characteristics of the tissue and found that all
above mentioned interictal patterns were most frequently seen
in areas containing dysmorphic neurons. These findings sug-
gest that the histological subtype may influence the interictal
electrographic patterns more than the localization or the pres-
ence of dual pathology.
ConclusionsSimultaneous recordings from the hippocampus and the TN
suggest that dysplastic tissue in the TN is often epileptogenic.
The quantitative contribution of the hippocampus to seizure
generation correlated strongly with the degree of hippocam-
pal pathology, whereas different subtypes of cortical dysplasia
did not affect its relative contribution to seizure generation in
our patient group. Even tissue with mild dysplastic features
(mMCD) in the TN could be epileptogenic. Moreover, the
interictal patterns recorded over the dysplastic TN showed
similarities to interictal patterns recorded over extratemporal
focal cortical dysplasias, additionally supporting epileptogeni-
city of these areas. To get more detailed information on the
significance of different types of temporo-neocortical dyspla-
sia in patients with hippocampal sclerosis larger patient
groups would be desirable.
Although MRI appears to be indicative of the relative role
of the AHC in seizure generation, the variable combination of
temporo-neocortical and limbic seizure onset warrants a pre-
cise definition of the epileptogenic area by invasive EEG
recordings if a tailored resection is aimed at.
AcknowledgementsThe authors thank PD Dr J. Honegger for the implantation of
the subdural strip electrodes, Prof. Dr C. Ostertag for the
implantation of the depth electrodes, Prof. Dr. B. Volk and
Dr G. Pantazis for providing the histological sections and
Prof. Dr M. Schumacher for high-resolution MRI.
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