Skip to main content

Temporal lobe epilepsy with amygdala enlargement: a subtype of temporal lobe epilepsy



Some recent studies suggest that some imaging-negative temporal lobe epilepsy (TLE) had significant amygdala enlargement (AE). Contradictory data were also reported in previous studies regarding the association between AE and TLE. The present study was to investigate the clinical characters of a group of TLE with AE and compare the amygdala volume of the same patient before and after antiepileptic drugs treatment by a larger sample size.


This study recruited 33 mesial TLE patients with AE and 35 healthy volunteers. The clinical history, seizure semiology, electroencephalogram (EEG), fluorodeoxyglucose-positron emission tomography (FDG-PET) and amygdala volume were investigated. The amygdala volume were compared between ipsilateral and contralateral sides, TLE patients and 35 healthy controls, and patients at first and follow-up visit by 3.0 T MRI.


Average seizure onset age was 42.0 years (SD 14.3). All patients had complex partial seizures, fourteen had occasional generalized tonic-clonic seizures which often happened during sleep. Ninety percent patients suffered from anxiety or depression. Thirty percent patients had memory decline. Interictal epileptiform discharges appeared predominantly in the anterior or inferior temporal area ipsilateral to AE. Interictal FDG-PET showed regional glucose hypometabolism in the ipsilateral temporal lobe. No hippocampal sclerosis (HS) was suspected in all patients. 22 patients demonstrated good seizure control and significantly reduced volume of the enlarged amygdala after treatment (P < 0.01). The other 11 patients showed initial response to treatment, followed by a gradual increase in seizure frequency over time, and no volume change of the enlarged amygdala after treatment.


TLE with AE probably represents a distinct nosological and probably less homogeneous syndrome which is most likely a subtype of TLE without ipsilateral HS. The chronic and long lasting inflammatory processes or focal cortical dysplasia could lead to amygdala enlargement possibly.

Peer Review reports


The amygdala are located in the medial temporal lobe of human brain. They receive extensive nerve input from many different brain areas, such as many sensory areas, hippocampus, hypothalamus, thalamus, frontal lobe and so on [1]. Therefore, they can influence neuroendocrine, emotional, and cognitive aspects of biologic information processing. The amygdala play a crucial role in mediating affective behavior in humans and primates [2]. Some functional imaging studies showed that emotional information processing, for instance angry or happy facial expressions, activated the amygdaloid complex [3],[4]. In patients with major depression, there is increased metabolism in limbic areas, indicating an overactivation of the amygdala might be a trait marker of depression [5]. These findings demonstrate that the amygdala are critical brain structures for the emotional evaluation of specific sensory input on the background of individual experience.

Emotional disturbances and psychiatric problems are frequently encountered in patients with temporal lobe epilepsy (TLE) [6]. Previous studies demonstrated significant amygdala enlargement (AE) was associated with dysphoric disorder and psychosis in TLE patients without hippocampal sclerosis (HS) [7],[8]. Furthermore, one study proposed that psychosis in patients may develop on the background of the dysphoric disorder of TLE [8]. A neurophysiological study using intracranial recordings showed that 5% of mesial TLE (MTLE) patients had seizure onset in the amygdala [9]. Previous imaging studies reported that isolated unilateral amygdala damage was observed in about 8% of MTLE patients [10]. Therefore, the amygdala may not only be involved and affected in MTLE but may also be regarded as an epileptogenic focus of MTLE.

Recently, some studies reported AE was observed in "magnetic resonance imaging (MRI) negative" TLE [7],[8],[11],[12]. "MRI negative" TLE was defined by the absence of a neocortical lesion, normal hippocampal volumetry, and absence of any increased signal in the mesial temporal lobes on routine visual assessment, despite we cannot preclude completely that "MRI negative" TLE may have HS identified after epilepsy surgery [13]. However, some earlier studies found inconsistent results. For instance, the study performed by Kalviainen R et al. showed that the amygdala were decreased in volume by at least 20% in 19% of TLE patients [14]. Moreover, isolated amygdala sclerosis has been described in some more earlier studies [15],[16]. Up to date, a role for the amygdala as a focus of epilepsy has not been explicitly established, unlike TLE with HS. Considering that the above findings are inconsistent and the prior studies are confined to small number of TLE patients, this study aims to investigate the clinical significance of AE in "MRI negative" TLE patients detected by MRI and compare the amygdala volume of the same patient before and after treatment by a larger sample size.



We recruited 33 MTLE patients with AE (AE group) in our Comprehensive Epilepsy Center from June 2010 to April 2012. As a comparison for amygdala volume, 35 healthy volunteers (normal group, mean 43.1 (SD 12.3) years) were also recruited from the subjects who underwent 3.0 T MRI study during the same period. Informed consent to participate the study and for publication for clinical details were obtained from each subject enrolled, and the study was reviewed and approved by the ethics committee of Beijing Tiantan Hospital affiliated to Capital Medical University in the People's Republic of China.

MTLE with AE was diagnosed according to semiology and scalp electroencephalogram (EEG) recording, and by 3.0 T MRI, as described below. 3.0 T MRI confirmed AE in all patients, who had lateralized seizures thought clinically and electrically consistent with an origin in the temporal lobe ipsilateral to AE, as determined by the assessment and agreement of two epilepsy specialists. Patients in whom there was a high suspicion of tumorous disease where the enlarged amygdala apparently compressed the adjacent tissue or showed clear intensity changes in T2 weighed or FLAIR images were excluded. Patients with dual pathologies were also excluded from this study. All patients received 24-hour EEG recordings with sphenoidal electrodes using the 10-20 system of scalp electrode placement. Recordings included both waking and sleeping states. Interictal fluorodeoxyglucose positron emission tomography (FDG-PET) was also performed to support the clinical diagnosis. Localization of the epileptogenic zone was determined by converging seizure semiology, EEG, 3.0 T MRI, and FDG-PET. Time from the first seizure to the date of the present study was at least one year. AE group were followed up for half a year to one year and the amygdala volume were determined again at follow-up visit. In addition, the Montreal Cognitive Assessment (MoCA) was performed to test for cognitive impairment, Hamilton Anxiety Scale (HAMD) and Hamilton Anxiety Scale (HAMA) were used to test for depression and anxiety. We also tested for paraneoplastic or autoimmune limbic involvement in twenty-one patients aged equal to or greater than 40 years old by measuring antibodies against Hu, Yo, Ri, Ma2, CV2/CRMP5, NMDA-R, CASPR2, AMPA1-R, AMPA2-R, LGI1, and GABA2-R. In 12 patients, cerebrospinal fluid (CSF) and serum were tested, while serum only was tested in the other 9 patients who refused lumber puncture. Serum and CSF titers for antibodies against Hu, Yo, Ri, CV2/CRMP5, amphiphysin, and Ma2 were measured by immuno-dot-blotting using a commercial test. The antibodies against NMDA-R, CASPR2, AMPA1-R, AMPA2-R, LGI1, and GABA2-R were measured by indirect immunofluorescence.

MRI assessment and volumetric measurements

For AE group patients and normal volunteers, an MRI study was performed with a 3 T MR scanner during the same period. To preclude seizure induced brain lesions as far as possible, the scan time interval after seizure were seven days at least. The MRI assessment and amygdala volumetric measurements referred to Mitsueda-Ono's method [12].

Statistical analysis

Statistical analyses were performed using SPSS (version 13.0). Quantitative variables were expressed as mean ± SD or n (%). T test or Mann-Whitney test for independent samples was used for comparison of quantitative variables according to the test of normality. Amygdala volume were statistically analyzed by paired t tests between AE group and normal controls, the normal and abnormal side for each patient and also analyzed between the larger and smaller sides for the normal control group. We also compared the abnormal side amygdala volume in the same patient of AE group before and after treatment. All tests were performed at a level of significance of 5% (p < 0.05).


Clinical profiles of AE group

The patient group consisted of seventeen women and sixteen men, with an averaged seizure onset age of 42.0 years (SD 14.3). The duration from the first seizure to this MRI study varied from one year to twelve years (a median of 2 years). No patient had a history of febrile convulsions or early epileptogenic insults. All patients had temporal lobe complex partial seizures (CPSs) beginning with motionless staring and behavioral arrest, followed by oral alimentary or manual automatisms. Total CPS duration ranged from one to five minutes. Six patients reported auras; two reported a strange but indescribable feeling, one smelled blood, and three reported a nervous feeling in their heart. Fourteen of 33 patients had generalized tonic-clonic seizures occassionally, which often happened during sleep. The frequency of CPSs was at least once per month in 32 of 33 patients, while the other patient (patient number 1) had seizure once or twice a year. Ninety percent of patients suffered emotional problems such as anxiety or depression. It was noteworthy that the emotional problems appeared before or simultaneously with seizures. Thirty percent of patients reported memory decline. One patient tested positive for the LGI1 antibody in both blood and CSF, who got great improvement in seizure frequency and memory impairment after hormonotherapy.

In all patients, EEG recordings revealed interictal spikes localized primarily to sphenoidal electrodes or in the anterior temporal-inferior frontal region (F7/F8). Unilateral interictal epileptiform discharges (IEDs) were ipsilateral to the enlarged amygdala in 31 patients with confirmed unilateral AE, while the two patients with bilateral AE (patient number 12 and 16) showed bilateral IEDs. Two patients presented habitual seizures during EEG examination. The ictal EEG recordings showed that seizure onset was ipsilateral to the AE and appeared predominantly on the anterior temporal electrodes and sphenoidal electrodes.

By 3.0 T MRI, AE was detected on the right in fifteen patients, on the left in sixteen and bilaterally in two. The enlarged amygdala was iso- to slightly hyper-intense on 3.0 T FLAIR images and was not enhanced by gadolinium. No HS was suspected in any of these patients as assessed by a neuroradiologist and two investigators (R-J Lv and X-Q Shao). For these patients, interictal FDG-PET showed regional glucose hypometabolism in the anterior temporal lobe, especially in the mesial area and temporal pole ipsilateral to the AE side. The clinical and demographic features of the AE patient group were presented in Table 1.

Table 1 Clinical features of the 33 temporal lobe epilepsy patients with amygdala enlargement

Before visiting our hospital, nine patients were maintained on valproic acid (200-400 mg/day), seven on carbamazepine (100-300 mg/day), ten patients were treated only with so-called Traditional Chinese medicines' with unknown components and six were untreated with medicines. Carbamazepine (400-800 mg/day) or Oxcarbazepine (600-1200 mg/day) was prescribed to replace previous medications after visiting our hospital. All secondary tonic clonic seizures were well controlled thereafter and CPS frequency declined significantly in 22 of 33 patients. Levetiracetam was added to carbamazepine or oxcarbazepine in the 11 patients who did not show a significant decline in CPS frequency. After half a year to one year follow up, 22 patients became seizure free (drug responsive patient group), however the other 11 patients adding levetiracetam (drug non-responsive patient group) showed initial response to treatment, followed by a gradual increase in CPSs seizure frequency over time. Although the seizure of most patients was not frequent, they continued to experience emotional and memory problems. Fifteen patients were diagnosed with clinical anxiety and/or depression according to ICD-10 criteria and were prescribed selective serotonin reuptake inhibitors.

Results of 3 T MRI amygdala volumetry

Table 2 showed the amygdala volume of all patients in the AE group and normal group determined by 3.0 T MRI. On the side of the enlarged amygdala with the seizure focus as determined by IEDs (ipsilateral), amygdala volume ranged from 1277.2 mm3 to 2046.6 mm3 (mean 1694.2 (SD 221.2) mm3). On the contralateral side, amygdala volume was smaller and ranged from 651.0 mm3 to 1494.2 mm3 (mean, 1213.7 (SD 232.6) mm3). There was a significant difference between the two sides (p < 0.01).

Table 2 Comparison of amygdala volume among the groups

In normal subjects (n = 35), the smaller side ranged from 760.3 mm3 to 1356.2 mm3 (mean 1202.8 (SD 112.3) mm3), while the larger side ranged from 836.4 mm3 to 1434.2 mm3 (mean 1298.2 (SD 122.5) mm3). There was no significant difference between the two sides (p > 0.05).

Amygdala volume of the affected side in the patient group and larger side in the normal group were compared, and it was significantly larger in AE group (p < 0.01).

Follow-up 3.0 T MRI was performed in all patients half a year to one year after the first MRI. The affected side amygdala volume at follow-up visit ranged from 930.2 mm3 to 1550.4 mm3 (mean 1306.2 (SD 172.4) mm3). Drug responsive patient group showed significantly decreased volume of the enlarged amygdala after treatment (p < 0.01). However, drug non-responsive patient group demonstrated no volume change of the enlarged amygdala after treatment (p > 0.05).

Figure 1.A showed a representative image of drug responsive AE group by 3 T MRI. Figure 1.B was the image of the same patient after one year treatment (patient number six). Figure 1.C showed a representative image in drug non-responsive AE group. Figure 1.D showed no change of amygdala volume of the same patient after one year treatment (patient number twenty-eight).

Figure 1

Axial FLAIR MRI in patient number six (A and B) in drug responsive AE group, and patient number twenty-eight (C and D) in drug non-responsive AE group before and after treatment. (A) Open circle indicates a representative image of left amygdala enlargement in drug responsive AE group. (B) Open circle indicates decreased amygdala volume in the same patient after one year of treatment. (C) Open circle indicates a representative image of right amygdala enlargement in drug non-responsive AE group. (D) Open circle indicates no change of amygdala volume of the same patient after a year treatment.


Up to date, there have been few amygdala volumetric studies, partly because of the amygdala's poorly demarcated anatomical boundaries [17],[18]. However, the method of amygdala volume measurement used in this study is now well established [7],[8],[11],[12]. The amygdala volumetry was determined in both patients and controls by the same epilepsy specialist (R-J Lv), therefore there was no inter-rater difference or bias. This study is a larger sample size report of TLE patients with increased amygdala volume. We obtained a similar finding in TLE patients with later onset age to the study performed by Mitsueda-Ono T et al. [12]. Our normal ranges and amygdala volume ratios are consistent with recently reported data [12].

In the present study, we found all TLE patients with enlarged amygdala ipsilateral to the IEDs except two patients with bilateral AE showed bilateral IEDs. Although only two patients had ictal EEG, most patients in our study presented unilateral IEDs ipsilateral to AE. Some studies indicated that IEDs in TLE can correlate very well with ictal onset zone, and about ninety percent focal spikes were ipsilateral to epilpeptogenic zone [19],[20]. Therefore, we have reason to speculate that most patients of our study presented localized anterior-inferior IEDs always consistent with the side of AE is not accidental phenomena. It may have potential hint that the seizures of 31 patients in our study were lateralized to the hemisphere containing the enlarged amygdala. There was some evidence demonstrating the effect of seizures to MR images which resolved and turned to normal after some time [21],[22]. Thus, the decreased volume of the enlarged amygdale at follow-up visit may suggest that AE may be epilpeptogenic zone conversely. The results of this study, combined with previous electrophysiological and radiological studies [11],[12],[23],[24], indicate that AE may function as an epileptogenic focus in this subgroup of TLE patients. However, we did not get direct recording from the amygdala by means of depth electrodes and also we did not have ictal single proton emission computed tomography (SPECT), thus we could not definitively demonstrate that the enlarged amygdala was epilpeptogenic zone. This needs further study according to more direct testimony such as invasive intracranial electrodes recording.

The mechanisms leading to amygdala enlargement in TLE are a matter of debate. A recent study reported the chronic and long lasting inflammatory processes with or without a self-limited course occurred in these TLE patients could lead to amygdala enlargement possibly [12]. Neuroinflammatory processes have been reported to be one of the causes of adult-onset TLE [25]. Autoimmune-mediated encephalitis has been characterized in middle-aged patients with TLE, and some patients demonstrated a self-limited course [25]-[27]. In our study, one patient had autoimmune limbic involvement and exhibited great improvements in seizure frequency and memory after immunotherapy, which suggested neuroinflammatory processes participated in amygdala enlargement possibly. Whereas, there were not paraneoplastic or autoimmune limbic involvement found in most patients, perhaps because the tests used for paraneoplastic or autoimmune were not comprehensive enough or owing to ethnic difference. That was the cause that we did not give immunotherapy to most patients. The emotional problems appeared before or simultaneously with seizure in this group of patients, which was similar to the report of limbic encephalitis [28], supporting that the etiology was autoimmune inflammation in some patients possibly. In addition, most patients (22 of 33 patients) showed significantly decreased volume of the enlarged amygdala without immune modulating treatment, which was similar to Mitsueda-Ono's study [12]. Some studies reported that seizure can induce brain lesions [29],[30]. Therefore, MRI scan were performed seven days after seizure at least to preclude seizure induced brain lesions as far as possible. Although we cannot preclude seizure related functional change completely because of the short follow-up time, the decreased volume of the enlarged amygdale at follow-up visit may suggest a self-limited course of neuroinflammation. In this study, the seizure onset was late, and FDG-PET scanning was performed within a few years after onset. This may imply that the epileptogenicity in the amygdala was mild and developed slowly. This assumption was consistent with the fact that seizures have been well controlled with a low dose of AEDs instead of immune modulating treatment in these TLE patients with AE. The assumption of long-lasting mild epileptic activity in the amygdale may be a clue to speculate that the possible etiology of AE was the chronic and long lasting inflammatory processes. However, the therapeutic effect declined gradually with follow-up time prolonging in some patients (11 patients), whose amygdala volume did not change after treatment. Therefore, the AE patients in our study could be heterogenous in etiology. Focal cortical dysplasia (FCD) cannot be precluded in some patients completely, especially those patients showing a decline in therapeutic efficacy. Similarly, a recent study found that FCD and low-grade tumors were major causes of late-onset TLE with AE [31]. The speculated reasons are very similar to the the most recent study [32]. However, it must be emphasized that these interpretations are very speculative and until now, there are no generally accepted models that can explain the mechanism leading to the phenomena of enlarged amygdala. This still need be studied further.

TLE with AE may define a subgroup of "imaging-negative" TLE patients that are clinically different to those with HS. Our patients were all late onset and exhibited fewer secondary generalized seizures compared to those patients with HS, consistent with Bruton's series [33]. With regard to ictal semiology, similar to Mitsueda-Ono's study [12], complex partial seizures were the most common sizure type. This group of patients had obvious affective disturbances from the onset of the diseases, mainly manifesting as dysthymia, in accordance with the findings of Tebartz van Elst L [7]. The affective disturbance was different from the general meaning of psychosis because they can be well controlled by antidepressant combined with AEDs. After AEDs treatment, most patients became seizure free or showed a dramatic improvement in seizure occurrence. Seizures are currently well controlled on anticonvulsant medication, a dissimilar situation to the usual natural history of TLE with HS, that was the reason we can not get further pathological results to confirm the mechanism leading to AE. In this group of patients, secondarily generalized seizures often occurred at night. To our knowledge, there are no similar findings reported in the literature and we currently have no plausible explanation for this finding. Further research is needed to replicate this finding.


These findings do have very important implications for the way we think about the diagnosis of "imaging-negative" TLE. TLE with AE probably represents a distinct nosological and probably less homogeneous syndrome which is most likely a subtype of TLE without ipsilateral HS. If there is no apparent HS in TLE patients, AE should be considered first.

Authors' contributions

Study concept and design (LRJ); acquisition of data (Drs LRJ, SXQ, CT, SZR, GHZ, RHT); analysis and interpretation of data (LRJ and SXQ); drafting of the manuscript (LRJ); Critical revision of the manuscript for important intellectual content (LRJ and SXQ); statistical expertise (LRJ); administrative, technical, and material support (LRJ, RHT and SXQ); study supervision (LRJ and SXQ). All authors read and approved the final manuscript.



Temporal lobe epilepsy


Amygdala enlargement




Fluorodeoxyglucose-positron emission tomography


Hippocampal sclerosis


Mesial temporal lobe epilepsy


Magnetic resonance imaging


Montreal Cognitive Assessment


Hamilton Anxiety Scale


Hamilton Anxiety Scale


Complex partial seizures


Interictal epileptiform discharges


Single proton emission computed tomography


Focal cortical dysplasia


Antiepileptic drugs


  1. 1.

    Pan JW, Spencer DD, Kuzniecky R, Duckrow RB, Hetherington H, Spencer SS: Metabolic networks in epilepsy by MR spectroscopic imaging. Acta Neurol Scand. 2012, 126 (6): 411-420. 10.1111/j.1600-0404.2012.01665.x.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  2. 2.

    Aggleton JP: The contribution of the amygdala to normal and abnormal emotional states. Trends Neurosci. 1993, 16 (8): 328-333. 10.1016/0166-2236(93)90110-8.

    CAS  Article  PubMed  Google Scholar 

  3. 3.

    Morris JS, Frith CD, Perrett DI, Rowland D, Young AW, Calder AJ, Dolan RJ: A differential neural response in the human amygdala to fearful and happy facial expressions. Nature. 1996, 383 (6603): 812-815. 10.1038/383812a0.

    CAS  Article  PubMed  Google Scholar 

  4. 4.

    Schneider F, Grodd W, Weiss U, Klose U, Mayer KR, Nagele T, Gur RC: Functional MRI reveals left amygdala activation during emotion. Psychiatry Res. 1997, 76 (2-3): 75-82. 10.1016/S0925-4927(97)00063-2.

    CAS  Article  PubMed  Google Scholar 

  5. 5.

    Ho AP, Gillin JC, Buchsbaum MS, Wu JC, Abel L, Bunney WE: Brain glucose metabolism during non-rapid eye movement sleep in major depression. A positron emission tomography study. Arch Gen Psychiatry. 1996, 53 (7): 645-652. 10.1001/archpsyc.1996.01830070095014.

    CAS  Article  PubMed  Google Scholar 

  6. 6.

    Trimble MR, Ring HA, Schmitz B: Neuropsychiatric Aspects of Epilepsy. Neuropsychiatry. Edited by: Fogel BS, Schiffer RB, Rao SM. 1996, William & Wilkins, Baltimore, 771-803.

    Google Scholar 

  7. 7.

    Tebartz Van Elst L, Woermann FG, Lemieux L, Trimble MR: Amygdala enlargement in dysthymia--a volumetric study of patients with temporal lobe epilepsy. Biol Psychiatry. 1999, 46 (12): 1614-1623. 10.1016/S0006-3223(99)00212-7.

    CAS  Article  PubMed  Google Scholar 

  8. 8.

    Tebartz Van Elst L, Baeumer D, Lemieux L, Woermann FG, Koepp M, Krishnamoorthy S, Thompson PJ, Ebert D, Trimble MR: Amygdala pathology in psychosis of epilepsy: a magnetic resonance imaging study in patients with temporal lobe epilepsy. Brain. 2002, 125 (Pt 1): 140-149. 10.1093/brain/awf008.

    CAS  Article  PubMed  Google Scholar 

  9. 9.

    Wieser HG: Mesial temporal lobe epilepsy versus amygdalar epilepsy: late seizure recurrence after initially successful amygdalotomy and regained seizure control following hippocampectomy. Epileptic Disord. 2000, 2 (3): 141-152.

    CAS  PubMed  Google Scholar 

  10. 10.

    Goncalves Pereira PM, Oliveira E, Rosado P: Relative localizing value of amygdalo-hippocampal MR biometry in temporal lobe epilepsy. Epilepsy Res. 2006, 69 (2): 147-164. 10.1016/j.eplepsyres.2006.01.012.

    Article  PubMed  Google Scholar 

  11. 11.

    Bower SP, Vogrin SJ, Morris K, Cox I, Murphy M, Kilpatrick CJ, Cook MJ: Amygdala volumetry in "imaging-negative" temporal lobe epilepsy. J Neurol Neurosurg Psychiatry. 2003, 74 (9): 1245-1249. 10.1136/jnnp.74.9.1245.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  12. 12.

    Mitsueda-Ono T, Ikeda A, Inouchi M, Takaya S, Matsumoto R, Hanakawa T, Sawamoto N, Mikuni N, Fukuyama H, Takahashi R: Amygdalar enlargement in patients with temporal lobe epilepsy. J Neurol Neurosurg Psychiatry. 2011, 82 (6): 652-657. 10.1136/jnnp.2010.206342.

    Article  PubMed  Google Scholar 

  13. 13.

    Blumcke I, Thom M, Aronica E, Armstrong DD, Bartolomei F, Bernasconi A, Bernasconi N, Bien CG, Cendes F, Coras R, Cross JH, Jacques TS, Kahane P, Mathern GW, Miyata H, Moshé SL, Oz B, Özkara C, Perucca E, Sisodiya S, Wiebe S, Spreafico R: International consensus classification of hippocampal sclerosis in temporal lobe epilepsy: a task force report from the ILAE commission on diagnostic methods. Epilepsia. 2013, 54 (7): 1315-1329. 10.1111/epi.12220.

    Article  PubMed  Google Scholar 

  14. 14.

    Kalviainen R, Salmenpera T, Partanen K, Vainio P, Riekkinen P, Pitkanen A: MRI volumetry and T2 relaxometry of the amygdala in newly diagnosed and chronic temporal lobe epilepsy. Epilepsy Res. 1997, 28 (1): 39-50. 10.1016/S0920-1211(97)00029-6.

    CAS  Article  PubMed  Google Scholar 

  15. 15.

    Miller LA, McLachlan RS, Bouwer MS, Hudson LP, Munoz DG: Amygdalar sclerosis: preoperative indicators and outcome after temporal lobectomy. J Neurol Neurosurg Psychiatry. 1994, 57 (9): 1099-1105. 10.1136/jnnp.57.9.1099.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  16. 16.

    Hudson LP, Munoz DG, Miller L, McLachlan RS, Girvin JP, Blume WT: Amygdaloid sclerosis in temporal lobe epilepsy. Ann Neurol. 1993, 33 (6): 622-631. 10.1002/ana.410330611.

    CAS  Article  PubMed  Google Scholar 

  17. 17.

    Cendes F, Andermann F, Gloor P, Evans A, Jones-Gotman M, Watson C, Melanson D, Olivier A, Peters T, Lopes-Cendes I, Leroux G: MRI volumetric measurement of amygdala and hippocampus in temporal lobe epilepsy. Neurology. 1993, 43 (4): 719-725. 10.1212/WNL.43.4.719.

    CAS  Article  PubMed  Google Scholar 

  18. 18.

    Cendes F, Andermann F, Gloor P, Gambardella A, Lopes-Cendes I, Watson C, Evans A, Carpenter S, Olivier A: Relationship between atrophy of the amygdala and ictal fear in temporal lobe epilepsy. Brain. 1994, 117 (Pt 4): 739-746. 10.1093/brain/117.4.739.

    Article  PubMed  Google Scholar 

  19. 19.

    Blume WT, Borghesi JL, Lemieux JF: Interictal indices of temporal seizure origin. Ann Neurol. 1993, 34 (5): 703-709. 10.1002/ana.410340513.

    CAS  Article  PubMed  Google Scholar 

  20. 20.

    Pataraia E, Lurger S, Serles W, Lindinger G, Aull S, Leutmezer F, Bacher J, Olbrich A, Czech T, Novak K, Deecke L, Baumgartner C: Ictal scalp EEG in unilateral mesial temporal lobe epilepsy. Epilepsia. 1998, 39 (6): 608-614. 10.1111/j.1528-1157.1998.tb01429.x.

    CAS  Article  PubMed  Google Scholar 

  21. 21.

    Oh JB, Lee SK, Kim KK, Song IC, Chang KH: Role of immediate postictal diffusion-weighted MRI in localizing epileptogenic foci of mesial temporal lobe epilepsy and non-lesional neocortical epilepsy. Seizure. 2004, 13 (7): 509-516. 10.1016/j.seizure.2003.12.005.

    Article  PubMed  Google Scholar 

  22. 22.

    Briellmann RS, Wellard RM, Jackson GD: Seizure-associated abnormalities in epilepsy: evidence from MR imaging. Epilepsia. 2005, 46 (5): 760-766. 10.1111/j.1528-1167.2005.47604.x.

    Article  PubMed  Google Scholar 

  23. 23.

    Okada K, Akamatsu N, Hashimoto T, Uozumi T, Tsuji S: A case of right mesial temporal lobe epilepsy accompanied with ictal polyopsia. Rinsho shinkeigaku = Clinical neurol. 2004, 44 (1): 39-42.

    Google Scholar 

  24. 24.

    Mitsueda-Ono T, Ikeda A, Noguchi E, Takaya S, Fukuyama H, Shimohama S, Takahashi R: Epileptic polyopia with right temporal lobe epilepsy as studied by FDG-PET and MRI: a case report. J Neurol Sci. 2006, 247 (1): 109-111. 10.1016/j.jns.2006.04.010.

    Article  PubMed  Google Scholar 

  25. 25.

    Bien CG, Urbach H, Schramm J, Soeder BM, Becker AJ, Voltz R, Vincent A, Elger CE: Limbic encephalitis as a precipitating event in adult-onset temporal lobe epilepsy. Neurology. 2007, 69 (12): 1236-1244. 10.1212/01.wnl.0000276946.08412.ef.

    CAS  Article  PubMed  Google Scholar 

  26. 26.

    Malter MP, Helmstaedter C, Urbach H, Vincent A, Bien CG: Antibodies to glutamic acid decarboxylase define a form of limbic encephalitis. Ann Neurol. 2010, 67 (4): 470-478. 10.1002/ana.21917.

    Article  PubMed  Google Scholar 

  27. 27.

    Vincent A, Buckley C, Schott JM, Baker I, Dewar BK, Detert N, Clover L, Parkinson A, Bien CG, Omer S, Lang B, Rossor MN, Palace J: Potassium channel antibody-associated encephalopathy: a potentially immunotherapy-responsive form of limbic encephalitis. Brain. 2004, 127 (Pt 3): 701-712.

    PubMed  Google Scholar 

  28. 28.

    Soeder BM, Gleissner U, Urbach H, Clusmann H, Elger CE, Vincent A, Bien CG: Causes, presentation and outcome of lesional adult onset mediotemporal lobe epilepsy. J Neurol Neurosurg Psychiatry. 2009, 80 (8): 894-899. 10.1136/jnnp.2008.165860.

    CAS  Article  PubMed  Google Scholar 

  29. 29.

    Cianfoni A, Caulo M, Cerase A, Della Marca G, Falcone C, Di Lella GM, Gaudino S, Edwards J, Colosimo C: Seizure-induced brain lesions: a wide spectrum of variably reversible MRI abnormalities. Eur J Radiol. 2013, 82 (11): 1964-1972. 10.1016/j.ejrad.2013.05.020.

    CAS  Article  PubMed  Google Scholar 

  30. 30.

    Chhetri SK, Mathur S, Soh C, Gosal D: Seizure-induced MRI changes mimicking metastatic brain disease. J Clinical Neurosci Official J Neurosurg Soc Australasia. 2014, 21 (5): 869-872. 10.1016/j.jocn.2013.06.012.

    Article  Google Scholar 

  31. 31.

    Kim DW, Lee SK, Chung CK, Koh YC, Choe G, Lim SD: Clinical features and pathological characteristics of amygdala enlargement in mesial temporal lobe epilepsy. J Clin Neurosci. 2012, 19 (4): 509-512. 10.1016/j.jocn.2011.05.042.

    Article  PubMed  Google Scholar 

  32. 32.

    Takaya S, Ikeda A, Mitsueda-Ono T, Matsumoto R, Inouchi M, Namiki C, Oishi N, Mikuni N, Ishizu K, Takahashi R, Fukuyama H: Temporal lobe epilepsy with amygdala enlargement: a morphologic and functional study. J Neuroimaging Official J Am Soc Neuroimaging. 2014, 24 (1): 54-62. 10.1111/j.1552-6569.2011.00694.x.

    Article  Google Scholar 

  33. 33.

    Bruton C: The neuropathology of temporal lobe epilepsy. In., edn. New York: Oxford University Press; 1988: 29-81.

Download references


The authors would like to thank the patients and the healthy volunteers for participating in this study. This work was supported by the Natural Science Foundation of China (grant 81301119) and a grant from the Youth Foundation of Beijing Tiantan Hospital (KY2011-14).

Author information



Corresponding author

Correspondence to Xiao-Qiu Shao.

Additional information

Competing interests

The authors declare that they have no competing interest.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Authors’ original file for figure 2

Rights and permissions

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Lv, R., Sun, Z., Cui, T. et al. Temporal lobe epilepsy with amygdala enlargement: a subtype of temporal lobe epilepsy. BMC Neurol 14, 194 (2014).

Download citation


  • Amygdala enlargement
  • Amygdala volume
  • Temporal lobe epilepsy