Magnetic resonance imaging (MRI) volumetry in children with nonlesional epilepsy, does it help?
Egyptian Journal of Radiology and Nuclear Medicine volume 52, Article number: 35 (2021)
Epilepsy is a chronic condition characterized by repeated spontaneous seizures. It affects up to 1% of the population worldwide. Children with magnetic resonance imaging (MRI) negative (or “nonlesional”) focal epilepsy constitute the most challenging pharmacoresistant group undergoing pre-neurosurgical evaluation. Volumetric magnetic resonance imaging (VMRI) is a non-invasive brain imaging technique done to measure the volume and structure of specific regions of the brain. It is useful for many things, but primarily for discovering atrophy (wasting away of body tissue) and measuring its progression. The aim of this study is to assess role of volumetric magnetic resonance imaging in evaluation of nonlesional childhood epilepsy in which no specific findings detected in conventional MRI.
There were 20 children with normal MRI brain volumetry (33.3%) and 40 children (66.6%) with abnormal MRI brain volumetry.
Grey matter volume in the abnormal group was significantly higher (P value was 0.001*) than the normal group (mean ± S.D 934.04 ± 118.12 versus 788.57 ± 57.71 respectively). White matter volume in the abnormal group was significantly smaller (P value was < 0.0001*) than in the normal group (mean ± S.D 217.79 ± 65.22 versus 418.07 ± 103.76 respectively). Right hippocampus CA4-DG volume in the abnormal volume group was found to be significantly smaller (P value < 0.0001*) than that of the normal group volume (mean ± S.D 0.095 ± 0.04 versus 0.32 ± 0.36 respectively). Right hippocampus subiculum volume in the abnormal volume group were found to be significantly smaller (P value was < 0.0001*) than that of the normal group volume (mean ± S.D 0.42 ± 0.11 versus 0.84 ± 0.09 respectively). Thalamus volume in the abnormal group was significantly smaller (P value 0.048*) than in the normal group (mean ± S.D 10.235 ± 3.22 versus 11.82 ± 0.75 respectively). Right thalamus was significantly smaller (P value was 0.028*) than in the normal group (mean ± S.D 5.01 ± 1.62 versus 5.91 ± 0.39 respectively). The sensitivity of the right hippocampus subiculum volume and right hippocampus CA4-DG was 100%. The sensitivity of white matter volume and grey matter volume and thalamus was 85% and 75% and 55% respectively. The specificity of the right hippocampus subiculum volume and right hippocampus CA4-DG was 90% and 90% respectively. The specificity of the right hippocampus subiculum volume and right hippocampus CA4-DG and grey matter volume and white matter volume and total hippocampus and thalamus was 100%. The specificity of brain volume was 60%. The accuracy of the right hippocampus subiculum volume and right hippocampus CA4-DG was 100%. The specificity of white matter volume, grey matter volume, thalamus, total hippocampus, and brain volume was 97%, 87%, 65%, 61%, and 57% respectively.
Volumetric magnetic resonance imaging is a promising imaging technique that can provide assistance in evaluation of nonlesional pharmacoresistant childhood epilepsy.
Epilepsy is a chronic condition characterized by repeated spontaneous seizures. It affects up to 1% of the population worldwide .
Patients with magnetic resonance imaging (MRI) negative (or “nonlesional”) focal epilepsy constitute the most challenging pharmacoresistant group undergoing pre-neurosurgical evaluation .
The overall prevalence of nonlesional epilepsy in all surgical studies is ~ 26% .
Seizures are classified into either generalized or partial, with partial seizures being further divided into those without loss of consciousness (simple) and those where consciousness is lost or impaired (complex) .
Once patients have a diagnosis of epilepsy, it is critical to further classify these patients into lesional or nonlesional for treatment and prognostic reasons .
There is no standardized epilepsy imaging protocol in place among different institutions and hospitals; the primary clinical neuroimaging modality is MRI, with acquisition of a whole brain T1WI for imaging anatomy, and various T2-based acquisitions for detecting tissue pathology as FLAIR and GRE .
Volumetric magnetic resonance imaging (VMRI) is a non-invasive brain imaging technique done to measure the volume and structure of specific regions of the brain. It is useful for many things, but primarily for discovering atrophy (wasting away of body tissue) and measuring its progression .
Volumetric MRI, when used in conjunction with EEG, and neuropsychological studies enable patients with epilepsy to be treated in an appropriate, efficient, and cost-effective manner .
The aim of this study is to assess role of volumetric MRI in evaluation of nonlesional childhood epilepsy.
The institutional ethical committee board approved this prospective clinical study. A written consent was obtained for the current study, and the procedures were explained for parents. Total number of patients enrolled in this study was sixty epileptic patients (36 males and 24 females). Age range was (3–14 years old) (mean age 8.47 ± 3.15 years). The study was conducted in the time period from May 2019 to June 2020. Patients were clinically evaluated by parental interviewing and history taking including onset of seizures, type, frequency, duration, medications, and response to drugs. Also, comprehensive clinical examination highlighting neurodevelopmental assessment was done. EEG with different montages was done for all patients using a Nihon Kohden 8-channel conventional EEG machine. Ten to 20 international systems of electrode placement for diagnosing epilepsy. MRI of the brain including volumetric measures was performed to all patients. Inclusion criteria were pediatric patients with both clinical- and EEG-suggested diagnosis of epilepsy, no structural abnormalities in conventional MRI, and no seizures at least 72 h before MRI imaging. Exclusion criteria included post-operative patients, post head trauma patients, febrile convulsions, patient with evidence of MRI structural lesion which may be the cause of seizures, contraindications to anesthesia before MRI technique, and contraindications to MRI technique itself as children with cochlear implants. No contrast material was given to any of our patients.
No special preparation was needed. The examination was fully explained to the parents. All MRI studies were carried out using the same MRI machine Philips Ingenia 1.5 T, 16 channels coil, Philips medical systems. Scan time was about 12 min.
The epilepsy-dedicated research protocol included the following pulse sequences: T1WI 3D: sT1W_3D_TFE, FOV: covering whole brain (230 mm), voxel 1 × 1 × 1 mm isotropic, SNR = 1, Echo pulse sequence: gradient, flip angle 30, TE 3.4 ms, TR 7.3 ms; T2W_3D_DRIVE: FOV: covering whole brain (230 mm), voxel 1 × 1 × 1 isotropic, SNR = 1, TE 245 ms, TR 1500 ms, SNR = 1; 3D FLAIR: FOV 230, voxel 1.16 × 1.44 × 5 mm, TR 11,000 ms, TE140 ms, SNR = 1
Conventional assessment was done using Philips ISP (Intellispace portal v. 9), for primary reporting.
Volumetric and segmentation reporting
A compressed T1WI dataset in NIFTI (Neuroimaging Informatics Technology Initiative) format was uploaded to online MRI-brain volumetric system at www.volbrain.com (VolBrain version 1.0 for whole brain segmentation and HIPS version 1.0 hippocampus segmentation). When automatic process is complete, a PDF report is created containing volumetric data about the grey matter, white matter, CSF, and subcortical grey matters as well as hippocampus segmentations.
We validate NIFTI files using the ITK-SNAP Version 3.4.0 software for all cases; full description of VolBrain pipe-line was published by Manjon and Coupé .
Once the process is finished, we were notified by e-mail, so we were able to download a package including some image files and two (CSV and PDF) reports gathering all the volumetry values calculated from the segmentations. In each report, volumes were measured such as: (1) volBrain report: parenchyma, brain tissues, macrostructure, and subcortical structure volumes measured such as volumes of the main intracranial cavity (ICC) tissues (that is, cerebrospinal fluid (CSF), grey matter (GM), and white matter (WM)). It also provides volume information of some macroscopic areas such as brain hemispheres, cerebellum, brainstem, and thalamus, finally, automatic subcortical structure segmentation and also asymmetry indexes. (2) Lesion brain report: lesion classes, volumes, and their locations; (3) hippocampus report: subfield volumes of hippocampus CA1-3, CA4-DG, and subiculum. The report also includes several snapshots from the different labeling results as a quality control. All the volumes were presented in absolute value (measured in cm3) and in relative value (measured in relation to the ICV). The asymmetry index is calculated as the difference between the right and left volumes divided by their mean (in percent). Values between brackets show expected limits (95%) of normalized volume in function of sex and age for each measure for reference purpose. Green and red values indicate that the volume is above or under the expected volume limits respectively.
Statistical analysis of the data
Data were fed to the computer and analyzed using the SPSS software package version 20.0. Cleaning of data as a first step was done to detect missing values and invalid responses. Qualitative data were described using frequency, number, and percent. Quantitative data were described using mean, standard deviation, and range (minimum and maximum). Significance of the obtained results was judged at the 5% level.
The Chi-square test and Fisher exact test “used if more than 20% of cells are less than 5” were used to compare between proportions. Student’s t test was used to compare two means.
Diagnostic accuracy was represented using the term sensitivity, specificity, positive predictive value, negative predictive value, and overall accuracy. P value less than 0.05 was considered statistically significant, and all statistical tests were 2 tailed.
According to the volumetric results, we classified epileptic patients who had shown normal conventional brain MR imaging into two groups: abnormal volume group (group A) and normal volume group (group B).
Group A included 40 patients (66.6%) and group B included 20 patients (33.3 %). The mean age for group A was 7.25 ± 3.39 (P 0.39) and mean age for group B was 8.2 ± 2.48. Generalized epilepsy was more common than focal epilepsy in group A (75% generalized epilepsy versus 25% focal epilepsy). On the other hand in group B patients, generalized epilepsy was 30% versus 70% focal epilepsy. Volumetric measures of different brain regions in the studied group A (N = 40) are given in Table 1. Volumetric measures of different brain regions in group B (N = 20) are given in Table 2.
Seizure frequency was 1.8 ± 0.85 with a range of attacks from 1 to 3 attacks/week and seizure duration ranged from 15 to 45 s. Seizure frequency in group A was significantly higher than in group B (mean ± S.D 2.05 ± 0.89 versus 1.30 ± 0.48 respectively). Age and sex showed no statistically significant difference between both groups.
Grey matter volume in group A was significantly higher (P value was 0.001*) than group B (mean ± S.D 934.04 ± 118.12 versus 788.57 ± 57.71 respectively) (Fig. 4). White matter volume in group A was significantly smaller (P value was < 0.0001*) than in group B (mean ± S.D 217.79 ± 65.22 versus 418.07 ± 103.76 respectively) (Fig. 1). Right hippocampus CA4-DG volume in group A was found to be significantly smaller (P value < 0.0001*) than that of group B (mean ± S.D 0.095 ± 0.04 versus 0.32 ± 0.36 respectively) (Fig. 2). Right hippocampus subiculum volume in group A was found to be significantly smaller (P value was < 0.0001*) than that of group B (mean ± S.D 0.42 ± 0.11 versus 0.84 ± 0.09 respectively). Thalamus volume in group A was significantly smaller (P value 0.048*) than in group B (mean ± S.D 10.235 ± 3.22 versus 11.82 ± 0.75 respectively) (Fig. 3). Right thalamus was significantly smaller (P value was 0.028*) than that found in group B (mean ± S.D 5.01 ± 1.62 versus 5.91 ± 0.39 respectively). Comparison between group A and B regarding volumetric measures is given in Table 3.
There was significant difference between EEG abnormalities and the volumetric measurements in the white matter volume and in the right hippocampus CA4-DG volume in the studied groups (P value was 0.03* and 0.02* respectively).
There was a fair to moderate positive correlation between most of the volume measured structures and the frequency of seizures reaching a significant level at brain volume (P 0.04), grey matter volume (P 0.0001), total hippocampus volume (0.03), left hippocampus volume (0.01), and left hippocampus CA1-3 volume (0.006).
The sensitivity of right hippocampus subiculum volume and right hippocampus CA4-DG was 100%. The sensitivity of white matter volume and grey matter volume and thalamus was 85% and 75% and 55% respectively. The specificity of the right hippocampus subiculum volume and right hippocampus CA4-DG was 90% and 90% respectively. The specificity of the right hippocampus subiculum volume and right hippocampus CA4-DG and grey matter volume and white matter volume and total hippocampus and thalamus was 100%. The specificity of brain volume was 60%. The accuracy of the right hippocampus subiculum volume and right hippocampus CA4-DG was 100%. The specificity of white matter volume, grey matter volume, thalamus, total hippocampus, and brain volume was 97%, 87%, 65%, 61%, and 57% respectively (Table 4).
Epilepsy is a chronic neurological disorder characterized by recurrent unprovoked seizures. These seizures are transient signs and/or symptoms due to abnormal, excessive, or synchronous neuronal activity in the brain . Patients with nonlesional epilepsy constitute the most challenging group undergoing presurgical evaluation .
Volumetric MRI allows detection of subtle abnormalities of the brain that are difficult or impossible to reveal on visual inspection .
Several recent software tools have been developed to automatically obtain volumetric measures using different strategies. volBrain is a new software pipeline for volumetric brain analysis. This pipeline provides automatically volumetric brain information at different scales in a very simple web-based interface not requiring any installation or advanced computational requirements .
In the current study, volumetric and segmentation reporting were done using an online MRI-brain volumetric system at www.volbrain.com (volBrain version 1.0 for whole brain segmentation and HIPS version 1.0 hippocampus segmentation) using the automated method. Once the automatic process is complete, a PDF report was created containing volumetric data.
In the current study and on comparison between abnormal volume (group A) and normal volume group patients (group B) and regarding seizure frequency, we found that patients in group A have highly frequent seizures than those in group B.
Regarding seizure type, our study demonstrated that generalized epilepsy was more common than focal epilepsy in group A (75% generalized epilepsy versus 25% focal epilepsy). On the other hand, in group B patients, generalized epilepsy was 30% versus 70% focal epilepsy. The aforementioned results come in concordance with the study done by Debourdeau et al. ; in their study, they reported that generalized epilepsy was more common than partial epilepsy.
In our study, an abnormal EEG was found both in abnormal volume and normal volume group patients. This finding strengthens the fact that EEG is used in the diagnosis of epilepsy and continues to play a central role in both diagnosis and management of patients with seizure disorders.
The higher percentage of abnormal EEG in our study may be attributed to the highly frequent seizures that were recorded in our study as Farid et al.  stated that there are many factors that influence the recording of interictal epileptiform discharge in epileptic patients; among these factors is the frequency of seizures.
We proved a big role of volumetry in the diagnosis of epileptic patients that if their conventional MRI gives no pathology, we can diagnose them by volumetric MRI. In our study, the sensitivity of the right hippocampus subiculum volume and right hippocampus CA4-DG was 100%. The sensitivity of white matter volume and grey matter volume and thalamus was 85% and 75% and 55% respectively.
In agreement with high sensitivity of volumetric MRI in detection of hippocampus volume in epileptic patients was the study of Giorgio and his colleagues  which found that volumetric MRI was useful in the presurgical evaluation of the epileptogenic site in TLE, showing asymmetry of the hippocampal volume ipsilateral to the seizure focus with a sensitivity up to 95%.
Another study in 2012 done by Farid et al.  found that quantitative MR imaging-derived hippocampal asymmetries discriminated patients with temporal lobe epilepsy from control subjects with high sensitivity (86.7–89.5%) and specificity (92.2–94.1%).
We compared between groups A and B patients regarding the volumetric measurements, and we found a significant reduction in the volume of most measured areas including white matter, hippocampus CA4-DG and hippocampus subiculum, and thalamus; we also found a significant increase in the volume of grey matter.
Lee and his colleagues  investigated the possible associations between cognitive dysfunctions and regional grey matter/white matter volumes in patients with newly diagnosed pediatric epilepsy; they found that the most prominent structural abnormalities observed in newly diagnosed pediatric epilepsy were decreased GM volumes in the bilateral frontal areas, especially the left inferior frontal and right middle frontal gyri.
Beheshti and his colleagues  reported significant grey matter and white matter volume reductions in temporal lobe epilepsy patients with hippocampal sclerosis; they also observed a slight grey matter amygdala swelling in the right temporal lobe epilepsy patients without hippocampal sclerosis.
Bernasconi and his colleagues  reported that the hippocampal head, body, and the entorhinal and perirhinal cortices in epileptic patients were significantly reduced.
Guimarãesn and his colleagues  revealed that volume reduction in the hippocampus has been demonstrated in pediatric localization-related epilepsy, including mesial temporal lobe epilepsy (TLE) and extratemporal lobe epilepsy.
It has been reported that the thalamus as a part of the limbic network has well-developed anatomic connection with mesial temporal lobe structures , so it has been suggested that the thalamus plays an important role in the amplification and distribution of limbic seizures and hence the volumetric abnormalities that can be detected in the thalamus could be concluded as a result of recurrent seizures .
Bonilha and his colleagues  reported that juvenile myoclonic epilepsy patients exhibited significant volume reductions in thalamus. In 2018, Yoong and his colleagues  revealed that cognitive impairment in early onset epilepsy is associated with reduced thalamic volume. In our study, the thalamus had no significant difference in abnormal volume group of patients with generalized seizures than in the other groups of the study.
The observed volumetric changes of the thalamus in our study and others were congruent with the reported data which points to an increase in blood oxygenation level-dependent signal in both thalami during interictal epileptiform activity in idiopathic generalized epilepsy [26, 27]. These volumetric changes which were confined to the thalamus were explained by Aghakhani et al.  as the thalamus mediates motor functions via connections from the ventral anterior and lateral nuclei to the motor cortex, basal ganglia, and cerebellum.
On comparison between abnormal volume group and normal volume group patients with partial seizures regarding volumetric measurements, we found a smaller hippocampal volume and its parts and white matter volume in abnormal volume group patients than that of normal volume group (Fig. 4). Our result was in keeping with an Australian follow-up study which focused on epileptic diagnosed cases and demonstrated a significant hippocampal volume loss over a period of time . Szabo et al.  found that patients with chronic temporal lobe epilepsy tend to have hippocampal volume loss. On the other hand, Liu et al.  found no relevant difference in hippocampal volume or other brain pathology after a period of time from follow-up.
Holtkamp et al.  concluded in their follow-up study of patients with focal epilepsy that recurrent seizures do not cause hippocampal volume change. This difference may be argued to the different methodological approaches that had been employed.
In our study, the correlation between seizure frequency and volumetric measurements of patients with partial epilepsy revealed significant correlation between the seizure frequency and brain volume, grey matter volume, and hippocampus.
The results of Pulsipher and colleagues  found a significant correlation between seizure frequency and hippocampal volume in patients with temporal lobe epilepsy. We only detected a significant decrease in hippocampus volume on the epileptogenic side. This observation was consistent with prior findings .
Volumetric magnetic resonance imaging is a promising imaging technique that can provide assistance in evaluation of nonlesional childhood epilepsy that may change prognosis and line of management. Future prospective studies applying volumetric magnetic resonance imaging on a larger number of children are recommended to confirm the results of the present study and to establish the diagnostic accuracy of this technique, and the validation of the MRI volumetry tool is recommended in epileptic children as early as possible to detect any volumetric changes.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Magnetic resonance imaging
Fluid-attenuated inversion recovery
Temporal lobe epilepsy
Neuroimaging Informatics Technology Initiative
Sidhu MK, Duncan JS, Sander JW (2018) Neuroimaging in epilepsy. Curr Opin Neurol 31(4):371–378
Siegel AM, Jobst BC, Thadani VM, Rhodes CH, Lewis PJ, Roberts DW (2001) Medically intractable, localization-related epilepsy with normal MRI: presurgical evaluation and surgical outcome in 43 patients. Epilepsia 42(7):883–888
Téllez-Zenteno JF, Ronquillo LH, Moien-Afshari F, Wiebe S (2010) Surgical outcomes in lesional and non-lesional epilepsy: a systematic review and meta-analysis. Epilepsy Res 89(2-3):310–318
Wright NB (2001) Imaging in epilepsy: a paediatric perspective. Br J Radiol 74(883):575–589
Pardoe H, Kuzniecky R (2014) Advanced imaging techniques in the diagnosis of nonlesional epilepsy: MRI, MRS, PET, and SPECT: Advanced Imaging Techniques in the Diagnosis of Nonlesional Epilepsy. Epilepsy Curr 14(3):121–124
Seidenberg M, Kelly KG, Parrish J, Geary E, Dow C, Rutecki P (2005) Ipsilateral and contralateral MRI volumetric abnormalities in chronic unilateral temporal lobe epilepsy and their clinical correlates. Elilepsia 46(3):420–430
Watson C, Jack CR, Cendes F (1997) Volumetric magnetic resonance imaging: clinical applications and contributions to the understanding of temporal lobe epilepsy. Arch Neurol 54(12):1521–1531
Manjón and Coupé Manjón JV, Coupé P (2016) volBrain: an online MRI brain volumetry system. Front Neuroinform 10:30
Aun AAK, Mostafa AA, Fotouh AMA, Karam KS, Salem AA, Salem A (2015) Role of magnetic resonance spectroscopy (MRS) in nonlesional temporal lobe epilepsy. EJRNM 47(1):217–231
Giorgio A, De Stefano N (2013) Clinical use of brain volumetry. J Magn Reson Imaging 37(1):1–12
Debourdeau P, Gérome P, Zammit C, Saillol A, Aletti M, Bargues L, Cointet F (2004) Frequency of anticardiolipin, antinuclear and anti β2GP1 antibodies is not increased in unselected epileptic patients: a case-control study. Seizure 13(4):205–207
Farid N, Girard HM, Kemmotsu N, Smith ME, Magda SW, Lim WY et al (2012) Temporal lobe epilepsy: quantitative MR volumetry in detection of hippocampal atrophy. Radiology 264(2):542–550
Lee JH, Kim SE, C-h P, Yoo JH, Lee HW (2015) Gray and white matter volumes and cognitive dysfunction in drug-naïve newly diagnosed pediatric epilepsy. Biomed Res Int 2015:923861
Beheshti I, Sone D, Farokhian F, Maikusa N, Matsuda H (2018) Gray matter and white matter abnormalities in temporal lobe epilepsy patients with and without hippocampal sclerosis. Front Neurol 9:107
Bernasconi A, Bernasconi N, Natsume J, Antel S, Andermann F, Arnold DJB (2003) Magnetic resonance spectroscopy and imaging of the thalamus in idiopathic generalized epilepsy. Brain 126(11):2447–2454
Guimarãesn CA, Li LM, Rzezak P, Fuentes D, Franzon RC, Montenegro MA, Cendes F, Thomé-Souza S, Valente K, Guerreiro MM (2007) Temporal lobe epilepsy in childhood: comprehensive neuropsychological assessment. J Child Neurol 22(7):836–840
Allebone J, Kanaan R, Maller J, O'Brien T, Mullen SA, Cook M et al (2019) Bilateral volume reduction in posterior hippocampus in psychosis of epilepsy. J Neurosurg Psychiatry 90(6):688–694
Ji C, Zhu L, Chen C, Wang S, Zheng L, Li H (2018) Volumetric changes in hippocampal subregions and memory performance in mesial temporal lobe epilepsy with hippocampal sclerosis. Neurosci Bull 34(2):389–396
Kim JH, Kim JB, S-i S, Kim DWJNC (2017) Subcortical grey matter changes in juvenile myoclonic epilepsy. Neuroimag clin 17:397–404
Sone D, Sato N, Maikusa N, Ota M, Sumida K, Yokoyama K, Kimura Y, Imabayashi E, Watanabe Y, Watanabe M, Okazaki M, Onuma T, Matsuda H (2016) Automated subfield volumetric analysis of hippocampus in temporal lobe epilepsy using high-resolution T2-weighed MR imaging. Neuroimage clin 12:57–64
Natsume J, Bernasconi N, Andermann F, Bernasconi AJN (2003) MRI volumetry of the thalamus in temporal, extratemporal, and idiopathic generalized epilepsy. Neurology 60(8):1296–1300
Szabo C, Lancaster JL, Lee S, Xiong J-H, Cook C, Mayes B et al (2006) MR imaging volumetry of subcortical structures and cerebellar hemispheres in temporal lobe epilepsy. AJNR 27(10):2155–2160
Ciumas C, Savic IJN (2006) Structural changes in patients with primary generalized tonic and clonic seizures. Neurology 67(4):683–686
Bonilha L, Keller SS (2015) Quantitative MRI in refractory temporal lobe epilepsy: relationship with surgical outcomes. Quant Imaging Med Surg 5(2):204
Yoong M, Hunter M, Stephen J, Quigley A, Jones J, Shetty J, McLellan A, Bastin ME, Chin RFM (2018) Cognitive impairment in early onset epilepsy is associated with reduced left thalamic volume. Epilepsy Behav 80:266–271
Aghakhani Y, Bagshaw A, Benar C, Hawco C, Andermann F, Dubeau F et al (2004) fMRI activation during spike and wave discharges in idiopathic generalized epilepsy. Brain 127(5):1127–1144
Gotman J, Grova C, Bagshaw A, Kobayashi E, Aghakhani Y, Dubeau F (2005) Generalized epileptic discharges show thalamocortical activation and suspension of the default state of the brain. Proc Natl Acad Sci U S A 102(42):15236–15240
Briellmann RS, Berkovic SF, Syngeniotis A, King MA, Jackson GD (2002) Seizure-associated hippocampal volume loss: a longitudinal magnetic resonance study of temporal lobe epilepsy. Ann Neurol 51(5):641–644
Liu RS, Lemieux L, Bell GS, Sisodiya SM, Bartlett PA, Shorvon SD et al (2002) The structural consequences of newly diagnosed seizures. Ann Neurol 52(5):573–580
Holtkamp M, Schuchmann S, Gottschalk S, Meierkord H (2004) Recurrent seizures do not cause hippocampal damage. J Neurol 251(4):458–463
Pulsipher DT, Seidenberg M, Morton JJ, Geary E, Parrish J, Hermann BJE et al (2007) MRI volume loss of subcortical structures in unilateral temporal lobe epilepsy. Epilepsy Behav 11(3):442–449
Wu D, Chang F, Peng D, Xie S, Li X, Wenjing Z (2020) The morphological characteristics of hippocampus and thalamus in mesial temporal lobe epilepsy. BMC neurology 235:503
We gratefully acknowledge the hard work, efficiency, and devotion of our imaging technicians, which made this work possible.
No sources of funding
Ethics approval and consent to participate
This study was approved by the Research Ethics Committee of the Faculty of Medicine at Minia University in Egypt on 2019 (reference number is not applicable). All patients included in this study gave written informed consent to participate in this research.
Consent for publication
All patients included in this research gave written informed consent to publish the data contained within this study.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Abdelgawad, E.A., Mounir, S.M., Abdelhay, M.M. et al. Magnetic resonance imaging (MRI) volumetry in children with nonlesional epilepsy, does it help?. Egypt J Radiol Nucl Med 52, 35 (2021). https://doi.org/10.1186/s43055-021-00409-0