Longitudinal distribution of hippocampal atrophy in mesial temporal lobe epilepsy

1997 ◽  
Vol 27 (2) ◽  
pp. 101-110 ◽  
Author(s):  
Mark Quigg ◽  
Edward H Bertram ◽  
Theodore Jackson
2013 ◽  
Vol 119 (5) ◽  
pp. 1098-1104 ◽  
Author(s):  
Takehiro Uda ◽  
Michiharu Morino ◽  
Hirotaka Ito ◽  
Noriaki Minami ◽  
Atsushi Hosono ◽  
...  

Object Amygdalohippocampectomy is a well-established, standard surgery for medically intractable mesial temporal lobe epilepsy (MTLE). However, in the case of MTLE without hippocampal atrophy or sclerosis, amygdalohippocampectomy is associated with decreased postoperative memory function. Hippocampal transection (HT) has been developed to overcome this problem. In HT the hippocampus is not removed; rather, the longitudinal hippocampal circuits of epileptic activities are disrupted by transection of the pyramidal layer of the hippocampus. The present study describes a less invasive modification of HT (transsylvian HT) and presents the seizure and memory outcomes for this procedure. Methods Thirty-seven patients with MTLE (18 men and 19 women; age range 9–63 years; 19 with surgery on the right side and 18 with surgery on the left side; seizure onset from 3 to 34 years) who were treated with transsylvian HT were retrospectively analyzed. All patients had left-side language dominance, and follow-up periods ranged from 12 to 94 months (median 49 months). Seizure outcomes were evaluated for all patients by using the Engel classification. Memory function was evaluated for 22 patients based on 3 indices (verbal memory, nonverbal memory, and delayed recall), with those scores obtained using the Wechsler Memory Scale–Revised. Patients underwent evaluation of the memory function before and after surgery (6 months–1 year). Results Engel Class I (completely seizure free) was achieved in 25 patients (67.6%). Class II and Class III designation was achieved in 10 (27%) and 2 patients (5.4%), respectively. There were differences in memory outcome between the sides of operation. On the right side, verbal memory significantly increased postoperatively (p = 0.003) but nonverbal memory and delayed recall showed no significant change after the operation (p = 0.718 and p = 0.210, respectively). On the left side, all 3 indices (verbal memory, nonverbal memory, and delayed recall) showed no significant change (p = 0.331, p = 0.458, and p = 0.366, respectively). Conclusions Favorable seizure outcome and preservation of verbal memory were achieved with transsylvian HT for the treatment of MTLE without hippocampal atrophy or sclerosis.


Neurology ◽  
2003 ◽  
Vol 60 (3) ◽  
pp. 405-409 ◽  
Author(s):  
E. Kobayashi ◽  
M.D. D'Agostino ◽  
I. Lopes-Cendes ◽  
S.F. Berkovic ◽  
M.L. Li ◽  
...  

2020 ◽  
Vol 41 (6) ◽  
pp. 987-993
Author(s):  
F. Riederer ◽  
R. Seiger ◽  
R. Lanzenberger ◽  
E. Pataraia ◽  
G. Kasprian ◽  
...  

Epilepsia ◽  
2010 ◽  
Vol 51 ◽  
pp. 47-50 ◽  
Author(s):  
Rodrigo Secolin ◽  
Claudia Maurer-Morelli ◽  
Fernando Cendes ◽  
Iscia Lopes-Cendes

Author(s):  
Fabio Thadeu Ferreira ◽  
Eliane Kobayashi ◽  
Iscia Lopes-Cendes ◽  
Fernando Cendes

Background/Objective:Diffuse temporal lobe abnormalities can be observed on MRI of patients with mesial temporal lobe epilepsy (MTLE). Our objective was to perform qualitative and quantitative analyses of temporal lobe structures in patients with familial MTLE (FMTLE) and nonfamilial MTLE.Methods:Two groups of patients were ascertained: 67 FMTLE patients (14 with refractory seizures) and 30 patients with nonfamilial refractory MTLE. We performed qualitative analyses of MRI (with multiplanar reconstruction) and volumes of hippocampi and anterior temporal lobes in all patients, and in a normal control group of 23 individuals. We used the Chi-square test and ANOVA for statistical analyses.Results:We identified anterior temporal lobe abnormalities by visual analysis in only 4% of FMTLE patients and atrophy of the anterior temporal lobe by volumetric analysis in 19%. In the group of nonfamilial MTLE patients we found anterior temporal lobe abnormalities by visual analysis in 17% of patients and anterior temporal lobe atrophy in 13%. Hippocampal atrophy was present in 90% of FMTLE and in 83% of nonfamilial MTLE. No signs of cortical dysplasia were observed.Conclusion:Anterior temporal lobe atrophy and other abnormalities outside the mesial portion of temporal lobes were infrequent in both familial and nonfamilial MTLE patients. Despite the genetic basis, hippocampal atrophy in FMTLE is not associated with other abnormalities outside the mesial temporal regions.


2016 ◽  
Vol 128 ◽  
pp. 169-175 ◽  
Author(s):  
Anaclara Prada Jardim ◽  
Jeana Torres Corso ◽  
Maria Teresa Fernandes Castilho Garcia ◽  
Larissa Botelho Gaça ◽  
Sandra Mara Comper ◽  
...  

Epilepsia ◽  
2003 ◽  
Vol 44 (6) ◽  
pp. 807-814 ◽  
Author(s):  
Luciana Patrízia Andrade-Valença ◽  
Marcelo Moraes Valença ◽  
Luciana Torres Ribeiro ◽  
André Luís Mendes Matos ◽  
Letícia Viana Sales ◽  
...  

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