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Amygdalar enlargement in patients with temporal lobe epilepsy
  1. Takahiro Mitsueda-Ono1,
  2. Akio Ikeda1,
  3. Morito Inouchi1,
  4. Shigetoshi Takaya2,
  5. Riki Matsumoto1,
  6. Takashi Hanakawa3,
  7. Nobukatsu Sawamoto2,
  8. Nobuhiro Mikuni4,
  9. Hidenao Fukuyama2,
  10. Ryosuke Takahashi1
  1. 1Department of Neurology, Kyoto University Graduate School of Medicine, Kyoto, Japan
  2. 2Human Brain Research Centre, Kyoto University Graduate School of Medicine, Kyoto, Japan
  3. 3Department of Cortical Function Disorders, National Institute of Neuroscience, Kodaira, Tokyo, Japan
  4. 4Department of Neurosurgery, Kyoto University Graduate School of Medicine, Kyoto, Japan
  1. Correspondence to Dr A Ikeda, Department of Neurology, Kyoto University Hospital, 54 Shogoin-Kawaharacho, Sakyo-ku, Kyoto 606-8507, Japan; akio{at}kuhp.kyoto-u.ac.jp

Abstract

Objective The purpose of the study was to clarify the significance of amygdalar enlargement (AE) in patients with temporal lobe epilepsy (TLE) detected by MRI.

Methods 11 TLE patients (eight men, mean age 45.3 (SD 18.2) years) with AE treated at Kyoto University Hospital were studied. Clinical history, ictal semiology, EEG, fluorodeoxyglucose–positron emission tomography (FDG-PET), interictal single photon emission CT (SPECT) and MRI were investigated. Amygdalar volume measured by 3 T MRI and its laterality index (LI) were compared with the three other groups: normal controls, patients with partial epilepsy of non-TLE and mesial TLE with hippocampal sclerosis (HS).

Results Average age of onset was 39.8 years (SD 19.5). Eight had complex partial seizures and three had generalised seizures. Epileptiform discharges were found in the temporal area ipsilateral to the AE by EEG. Interictal FDG–PET/SPECT revealed regional hypometabolism or hypoperfusion in the ipsilateral temporal area. MRI showed AE on the right in five patients, on the left in five and bilateral in one, all without apparent HS. Ten of 11 patients were diagnosed as unilateral TLE ipsilateral to the AE by neurophysiological and neuroimaging methods. Enlarged amygdalae showed iso- to slightly high intensity in FLAIR images without enhancement. Unilateral AE was not seen in the other three groups for amygdalar volume and LI (p<0.05).

Discussion AE is most likely a subtype of TLE without ipsilateral HS. This possibility of AE should be considered in TLE patients if there is no apparent HS.

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Footnotes

  • Funding This study was supported by a Research Grant for the Treatment of Intractable Epilepsy (22-1) from the Japanese Ministry of Health, Labour and Welfare and by a Scientific Research Grant (C2) from the Japanese Society for Promotion of Science (JSPS).

  • Competing interests None.

  • Ethics approval This study was conducted with the approval of the Kyoto University Graduate School and Faculty of Medicine, Ethics Committee (Approval No. 463).

  • Provenance and peer review Not commissioned; externally peer reviewed.

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