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Epilepsy Research 38 (2000) 45 52

www.elsevier.com/locate/epilepsyres

Intracranial meningiomas and epilepsy: incidence, prognosis


and influencing factors
Ann-Shung Lieu, Shen-Long Howng *
Department of Neurosurgery, Kaohsiung Medical College Hospital, No. 100, Shih-Chuan 1st Road, Kaohsiung City 807, Taiwan,
ROC
Received 15 January 1999; received in revised form 15 June 1999; accepted 20 June 1999

Abstract

In a retrospective study of a consecutive series of 222 surgically treated meningiomas, it was found that 26.6% of
the patients presented epilepsy as their initial symptom. In this group, surgical excision of the intracranial
meningiomas stopped the epilepsy in about 62.7% of the patients. But approximately one-fifth of the patients with
intracranial meningiomas and no history of preoperative epilepsy developed new onset postoperative seizures. Of the
patients with early onset of postoperative epilepsy, epilepsy appeared in 66.7% within first 48 h after surgery. Of the
patients with postoperative epilepsy, 71.2% were seizure-free following 1 year of anticonvulsant therapy. Regarding
preoperative existing factors, intracranial meningiomas located at supratentorium, convexity, and with evidence of or
severe peritumoral edema significantly contributed to preoperative epilepsy. And in patients with preoperative
epilepsy, those tumors with evidence of or severe perifocal edema and cerebral edema at the operative site were
significantly more likely to suffer from postoperative epilepsy. 2000 Elsevier Science B.V. All rights reserved.

Keywords: Meningioma; Epilepsy; Incidence; Influencing factor

1. Introduction 1989; Yao, 1994; Chow et al., 1995). Surgical


removal of the tumor is the first choice of treat-
Intracranial meningiomas are common in- ment. The incidence and causes of preoperative
tracranial tumors, and epilepsy is one of the most and postoperative epilepsy have rarely been re-
common symptoms of intracranial meningiomas ported in the literature (Chan and Thompson,
with an incidence of 20 50% as the first symptom 1984; Chow et al., 1995). In this study, a consecu-
(Ramamurthi et al., 1980; Chan and Thompson, tive series of 222 cases of surgically treated in-
1984; Giombini et al., 1984a,b; Rohringer et al., tracranial meningiomas were retrospectively
reviewed. The incidence, prognosis, and influenc-
* Corresponding author. Tel.: + 886-7-3215049; fax: + 886- ing factors for preoperative and postoperative
7-3215039. epilepsy will be discussed.

0920-1211/00/$ - see front matter 2000 Elsevier Science B.V. All rights reserved.
PII: S 0 9 2 0 - 1 2 1 1 ( 9 9 ) 0 0 0 6 6 - 2
46 A.-S. Lieu, S.-L. Howng / Epilepsy Research 38 (2000) 4552

Table 1
Age and sex distribution

Age group Males Females Totala

Seizure no. Total Seizure no. Total

1019 1 2 1 1 3 (2)
2029 2 2 10 12 (2)
3039 3 10 5 22 32 (8)
4049 7 18 6 28 46 (12)
5059 7 21 12 37 58 (19)
6069 5 13 6 35 48 (11)
7079 1 7 3 16 23 (4)
Total 24 73 35 149 222 (59)

a
Numbers in parentheses represent total seizure cases in age group.

2. Materials and methods ings. The histologic classification was based on


the classification of Russell and Rubinstein
This is a retrospective study of 222 consecutive (1989).
patients with intracranial meningiomas surgically Statistical analysis was performed using chi-
treated between April, 1982 and April, 1997. The square test. A P-value of B 0.05 was considered
patients ranged in age from 12 to 79 years with a significant.
mean age of 51.9 years. The female to male ratio
was 2.2:1. Early postoperative seizure was defined
as the onset of epilepsy within 1 week of surgery, 3. Results
and late postoperative seizure was defined as on-
set of epilepsy beyond the first week of surgery. In our series, 59 (26.6%) patients presented
The amount of associated brain edema was epilepsy as their first clinical symptom. There
classified according to the method used by Go et were 35 females and 24 males with a mean age of
al. (1988) who classify it as absent, marginal, 50.2 years (range 1278 years old) (Table 1).
evident or severe depending on the extension of Statistically, our study demonstrates no difference
the peritumoral hypodense area in the brain com- in occurrence between sexes (P= 0.140). A total
puted tomographic (CT) scan. The location of of 188 tumors were located at the supratentorium
tumors was determined by brain CT scan, mag- with 57 (30.3%) of the patients presenting preop-
netic resonance image (MRI) or operative find- erative epilepsy. A total of 21 tumors were located

Table 2
Incidence of preoperative epilepsy relative to location

Localization Number of patients with epilepsy Total number of patients %

Cerebral convexity 33 81 40.7


Parasagittal/falx 14 51 27.5
Tuberculum sella 1 26 3.8
Sphenoid ridge 6 18 33.3
Olfactory groove 2 8 25.0
Tentorium 1 10 10.0
Posterior fossa 2 20 10.0
Multiple 3 0.0
Others 5 0.0
A.-S. Lieu, S.-L. Howng / Epilepsy Research 38 (2000) 4552
Table 3
Patients with epilepsy associated with location

Tumor location Total number Preoperative epilepsy No preoperative epilepsy


of cases
ORa (95% CI)a No. of cases (%) No. with postoperative No. of cases (%) No. with postoperative epilepsy
epilepsy (%) (%)

Frontalb 63 1.00 21 (33.3) 8 (38.1) 42 (66.7) 9 (21 4)


Temporal 22 2.40 (0.896.45) 12 (54.5) 5 (22.7) 10 (45.5) 2 (20.0)
Parietalc 33 1.14 (0.472.76) 12 (36.4) 4 (33.3) 21 (63.6) 8 (38.1)
Occipital 15 0.31 (0.061.49) 2 (13.3) 1 (50.0) 13 (86.7) 2 (15.4)

a
95% CI, 95% confidence interval; OR, odds ratio.
b
Including convexity, parasagittal/falx and olfactory groove.
c
Including convexity and parasagittal/falx.

47
48 A.-S. Lieu, S.-L. Howng / Epilepsy Research 38 (2000) 4552

at the infratentorium with only two (9.5%) of the tients, the epileptic pattern changed in five pa-
patients presenting preoperative epilepsy. The tients. In three patients, the preoperative
supratentorial tumors had significantly higher in- generalized seizure changed to partial seizure. In
cidence of preoperative epilepsy than infratento- the other two, the partial seizure changed to
rial tumors (P = 0.03). The relative incidence of generalized seizure. A total of 30 patients with no
preoperative epilepsy in different intracranial lo- history of preoperative epilepsy developed new-
cation is showed in Table 2. Tumors located at onset postoperative epilepsy. Among the 18 pa-
convexity, parasagittal/falx or sphenoid area had tients who developed early postoperative epilepsy,
significantly higher incidence of preoperative cerebral edema was found at surgical site in 15
epilepsy than others (P = 0.004). According to the patients and hematoma at operative site in six
location of frontal, temporal, parietal and occipi- patients. There were 34 patients who had late
tal lobe, our results demonstrate no significant postoperative epilepsy. A recurrence of tumors
difference (P= 0.077) but the incidence of preop- was noted in 13 of these patients. Regarding the
erative epilepsy in temporal lobe was eightfold factors affecting postoperative epilepsy, patients
higher than occipital lobe and twofold higher than with preoperative epilepsy, evidence of peritu-
frontal and parietal lobe (Table 3). moral edema and cerebral edema at the operative
Of these 165 patients, 94 had predominantly site had statistically significant associations with
right-sided and 71 left-sided lesions; 29 (30.9%) of the occurrence of postoperative epilepsy (Table 5).
the former and 25 (35.2%) of the latter had preop- The other factors have no significant effect.
erative epilepsy. There is no significant difference Of the 52 patients with postoperative epilepsy,
statistically (P=0.550) between right-sided and the follow-up periods ranged from 1 to 12 years.
left-sided intracranial meningiomas. During the follow-up periods, 37 (71.2%) patients
As regards peritumoral edema, of the 133 cases were seizure-free after 1 year of anticonvulsant
with no or slight edema, 26 cases presented preop- (phenytoin or valproic acid) therapy. A total of
erative epilepsy. Among 78 cases with evident or seven patients who all had late postoperative
severe edema, 31 patients had preoperative epilepsy had intermittent seizure attacks and eight
epilepsy, implying a correlation (P = 0.0009) be- patients had expired.
tween edema and epilepsy. Of the patients with
evidence of or severe peritumoral edema, 28 had
postoperative epilepsy. This figure is significantly
4. Discussion
higher than those with no peritumoral edema
(P =0.0014). Among these 28 patients, cerebral
Intracranial meningiomas account for approxi-
edema at operative site was noted in 11 patients
mately 20% of all intracranial tumors (Rachlin
and it was significantly related to the peritumoral
and Rosenblum, 1991). The incidence of epilepsy
edema (P=0.0462). The rate of preoperative
as the first symptom in intracranial meningiomas
epilepsy in different histological types was as fol-
lows: meningotheliomatous (19.3%), transitional
(37.9%), psammomatous (20%), fibroblastic
(25%), angioblastic (50%), atypical (50%) and oth- Table 4
Preoperation type of epilepsy
ers (40%). No correlation was observed (P =
0.199) between histological type and preoperative Type Number of cases
epilepsy.
Various preoperative seizure types are shown in Generalized seizure 40
Table 4. No patients had preoperative or postop- Partial seizure 16
Partial seizure with secondary 2
erative status epilepticus. A total of 52 patients
generalization
had postoperative epilepsy. Among them, 22 pa- Complex partial seizure 1
tients (37.3%) had had preoperative epilepsy Total 59
which continued postoperatively. Of these 22 pa-
A.-S. Lieu, S.-L. Howng / Epilepsy Research 38 (2000) 4552 49

Table 5
Factors affecting preoperative and postoperative epilepsy

Preoperation Postoperation

No. of patients No. of patients P-value No. of patients No. of patients P-value
with Ea with NEa with Ea with NEa

Sex
Female 35 114 0.140 33 116 0.52
Male 24 49 19 54
Age group (years)
1039 12 35 0.385 13 34 0.596
4059 24 80 25 79
6079 23 48 14 57
Location
Supratentorium 57 131 0.030 50 138 0.07
Infratentorium 2 19 2 19
Right 29 65 0.550 25 69 0.70
Left 25 46 17 54
Frontalb 21 42 0.077 17 54 0.499
Temporal 12 10 7 15
Parietalc 12 21 12 21
Occipital 2 13 3 12
Convexity 33 48 0.004 20 61 0.443
Parasagittal (or 14 37 16 45
falx)
Sphenoid ridge 6 12 6 12
Olfactory 2 6 3 5
Suprasellar 1 25 3 23
Cerebellopontine 1 13 2 12
Others 2 24 2 24
Peritumoral edema
Absent or mar- 26 108 0.0009 23 111 0.0014
ginal
Evident or severe 33 47 29 50
Pathology
Meningothelioma- 23 96 0.199 23 96 0.301
tous
Transitional 11 18 9 20
Psammomatous 5 20 2 23
Fibroblastic 2 6 1 7
Angioblastic 4 5 2 7
Atypical 4 8 4 8
Others 10 10 11 9
Preoperati6e E
Yes 59 22 0.025
No 163 30
Operation
Gross total re- 42 145 0.414
moval
Subtotal removal 10 25
Postoperati6e re-
currence
Yes 13 34 0.440
No 39 136

a
E, epilepsy; NE, no epilepsy.
b
Including convexity, Parasagittal/falx and Olfactory groove.
c
Convexity and parasagittal/falx.
50 A.-S. Lieu, S.-L. Howng / Epilepsy Research 38 (2000) 4552

is reported to be from 20 to 50% (Ramamurthi et Regarding the relationship between histological


al., 1980; Chan and Thompson, 1984; Giombini et types and preoperative epilepsy, while Chow et al.
al., 1984a,b; Rohringer et al., 1989; Yao, 1994; stated that histologic types were not significantly
Chow et al., 1995). In the present study, epilepsy correlated with preoperative epilepsy (Chow et al.,
is the most common clinical symptom and its 1995), Kawaguchi et al. believed that fibroblastic
incidence is 26.6%. Although the ratio of female meningiomas were (Kawaguchi et al., 1995).
to male patients with intracranial meningiomas is While our study finds that angioblastic menin-
2:1, our series and some reports (Chow et al., giomas have a high incidence of associated preop-
1995; Chozick et al., 1996) demonstrate no signifi- erative epilepsy, it does not demonstrate a
cant difference of preoperative epilepsy according significant difference between histological type
to sex (P = 0.14). In spite of the fact that the and preoperative epilepsy.
occurrence of epilepsy is not significantly different In our study, preoperative epilepsy is found to
(P= 0.385) in age group, it occurs more fre- be significantly related (P= 0.0009) to peritu-
quently in the fifth and sixth decades. moral edema, similar to a report by Kawaguchi et
The incidence of preoperative epilepsy in supra- al. (1995). It should be noted that peritumoral
tentorium has been reported to be from 29 to 67% edema fluid consists of excessive concentration of
(Ramamurthi et al., 1980; Chan and Thompson, glutamate and aspartic acid (Chan et al., 1979;
1984; Chozick et al., 1996); the incidence in our Fishman and Chan, 1980) which may be involved
series was 30.3%. The occurrence of preoperative in denervation hypersensitivity and propagation
of excitatory influences (Kawaguchi et al., 1995).
epilepsy in supratentorium is significantly higher
According to the literature, surgical removal of
than infratentorium (P =0.03). To the best of our
a meningioma eliminates epilepsy in 19.263.5%
knowledge, the difference in the occurrence of
of patients with preoperative epilepsy (Logue,
preoperative epilepsy between left and right hemi-
1974; Ramamurthi et al., 1980; Chan and Thomp-
spheric meningiomas has rarely been mentioned
son, 1984; Chozick et al., 1996), and postoperative
(Scott, 1985). Although the study of Scott showed
epilepsy develops in 5.142.9% of patients with
that patients with predominantly left-sided menin-
no history of preoperative epilepsy (Logue, 1974;
gioma showed a statistically significant greater
Foy et al., 1981; Chan and Thompson, 1984;
chance of developing seizures after operation Giombini et al., 1984a,b; Chow et al., 1995; Choz-
(Scott, 1985), the occurrence of preoperative or ick et al., 1996). In our present study, 37 (62.7%)
postoperative epilepsy is not significantly different patients enjoy complete cessation of epilepsy after
between right and left hemisphere lesions in our operation, and the incidence of patients with new-
series. The highest frequencies of preoperative onset epilepsy after surgery is 18.4%. In other
epilepsy are found in convexity, parasagittal/falx words, for patients with a meningioma and preop-
and sphenoid ridge meningiomas. These findings erative epilepsy, one can predict a postoperative
are similar to the report by Chow et al. (1995). cessation of convulsions in approximately 62.7%
Hoefer et al. reported that meningioma in the of the cases, and for those with no history of
temporal lobe did not produce any form of preop- preoperative convulsions almost 18.4% are likely
erative epilepsy (Hoefer et al., 1947, cited in Chan to develop postoperative seizures. In instances
et al., 1979), but our study shows temporal lobe of early onset, 66.7% of cases of postoperative
meningiomas have a higher incidence of preopera- epilepsy appeared within the first 48 h, a find-
tive epilepsy than frontal, parietal and occipital ing similar to that of Pasquet et al. (1976). During
lobe. Some authors (Flyger, 1956; Ramamurthi et follow-up periods, 71.2% of patients became
al., 1980; Chozick et al., 1996) have reported that seizure free after 1 year of anticonvulsant therapy.
meningioma in parietal lobe has a significantly There are seven patients (13%) who have late
higher incidence of postoperative epilepsy than postoperative epilepsy, who still have intermit-
others, but it did not appear to be significantly tent seizure attacks. Patients with early post-
different in the present study. operative epilepsy have a better prognosis than
A.-S. Lieu, S.-L. Howng / Epilepsy Research 38 (2000) 4552 51

late postoperative epilepsy. Although Chan et al. (Chozick et al., 1996). In our series, one case with
and Olivecrona reported postoperative status a cerebellopontine meningioma developed acute
epileptus in patients with intracranial menin- hydrocephalus and convulsion after operation.
giomas in their reports (Olivecrona, 1947; Chan et Patients with parietal tumors appear to be more
al., 1979), we have no instances of this. Factors susceptible to the development of new-onset post-
that have been associated with the development of operative epilepsy (Ramamurthi et al., 1980;
postoperative epilepsy after intracranial menin- Chozick et al., 1996). In our study, the preopera-
gioma operation include brain retraction, inter- tive epilepsy in 66.7% of our patients with parietal
ruption of cortical veins, arterial damage, meningiomas was resolved whereas 38.1% of pa-
preoperative epilepsy history, extent of tumor re- tients with a parietal meningioma and no history
moval, and postoperative hydrocephalus as well of epilepsy developed postoperative epilepsy.
as parietal location (Logue, 1974; Ramamurthi et Overall, 26.7% of our patients with new-onset
al., 1980; Foy et al., 1981; Chan and Thompson, postoperative epilepsy had parietal meningioma,
1984; Chow et al., 1995; Chozick et al., 1996). In much less than the series reported by Chozick et
our study, a history of preoperative epilepsy, evi- al.
dence of peritumoral edema and cerebral edema
at operative site play significant roles in postoper-
ative epilepsy. About 37.3% of the patients with a 5. Conclusions
history of preoperative epilepsy suffered postoper-
ative epilepsy, making it a significant (P = 0.025) From the present study, it is found that there is
contributing factor to postoperative epilepsy. In- a significant incidence of preoperative epilepsy in
tracranial meningiomas with evidence of or severe patients with meningiomas located at supratento-
peritumoral edema was also a significant (P = rium or evident/severe peritumoral edema. In
0.0014) influencing factor for postoperative about 62.7% of patients with preoperative
epilepsy. In the present series, tumors with evi- epilepsy, the epilepsy could be eliminated by sur-
dence of or severe perifocal edema associated gical excision. Approximately one-fifth of patients
significantly with cerebral edema at the operative with a meningioma and no history of preoperative
site (P=0.0462), and thus also have an influence, convulsions were likely to develop postoperatively
especially in the early onset of postoperative new-onset seizures. Patients with parietal tumors
epilepsy, which is an observation previously made and no history of preoperative epilepsy had a high
by others (Tsuji et al., 1993; Chow et al., 1995). incidence of new-onset of postoperative epilepsy.
Surgical manipulation and slow resolution of per- Of our patients with postoperative epilepsy 70%
ifocal edema may be the cause of cerebral edema enjoyed good control of seizures with anticonvul-
at operative site. In 33% of our patients with early sant therapy, which can be tapered off and then
onset of postoperative epilepsy, hematoma at op- discontinued entirely over a 1-year period. Preop-
erative site was found, possibly indicating it may erative epilepsy, evidence of peritumoral edema
have something to do with the early onset of and cerebral edema at operative site are important
postoperative epilepsy. Chozick et al. (1996) predisposing factors for postoperative epilepsy.
thought that subtotally resected tumor was a sig-
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