Vol 58, No 3 (2024)
Invited Editorial
Published online: 2024-03-14

open access

Page views 381
Article views/downloads 286
Get Citation

Connect on Social Media

Connect on Social Media

INVITED EDITORIAL

Neurologia i Neurochirurgia Polska

Polish Journal of Neurology and Neurosurgery

2024, Volume 58, no. 3, pages: 215–217

DOI: 10.5603/pjnns.99781

Copyright © 2024 Polish Neurological Society

ISSN: 0028-3843, e-ISSN: 1897-4260

Lesional mesial temporal lobe epilepsy in children: is there a superior surgical approach?

Marek ManderaŁukasz Antkowiak
Department of Paediatric Neurosurgery, Medical University of Silesia in Katowice, Katowice, Poland

Address for correspondence: Marek Mandera, Department of Paediatric Neurosurgery, Medical University of Silesia in Katowice, Medyków 16 St., 40752 Katowice, Poland; e-mail: mmandera@sum.edu.pl

Received: 25.02.2024 Accepted: 26.02.2024 Early publication date: 14.03.2024

Epilepsy constitutes the most prevalent chronic neurological disorder in the paediatric population, with a worldwide prevalence of 0.9% [1, 2]. Despite continuous advances in the field of antiepileptic drugs (AEDs), up to 25% of paediatric patients suffer from drug-resistant epilepsy (DRE) [3]. According to surgical series, temporal lobe epilepsy (TLE) forms the most common type of DRE [4, 5]. That specific disorder constitutes 1020% of all epilepsy cases in the paediatric population [6]. The pathological background of TLE in children is mainly associated with the existence of low-grade gliomas (LGGs), cortical dysplasia (CD), vascular malformations, and, although less frequently than in adults, mesial temporal sclerosis (MTS) [6–8]. Importantly, 80% of TLE originates from the mesial temporal lobe (MTL), and this is known as mesial temporal lobe epilepsy (mTLE). Surgery for drug-resistant TLE remains the most effective therapeutic strategy [9–12]. According to recent reports, after surgical intervention 6785% of paediatric patients can be free from disabling seizures (Engel class I), while 6178% of children can achieve complete seizure freedom (Engel class IA) [9, 13, 14].

Surgical strategy for tumour-related mTLE depends on the location of the lesion itself and the coexistence of epileptogenic foci unrelated to the tumour. The quest for less destructive resections has led to more selective approaches to the MTL being adopted, including lesionectomy (where resection is limited to the tumour) and extended lesionectomy (tumour with the peritumoural area) [4, 14–16]. Various surgical corridors have been explored in order to achieve the MTL’s desired anatomical location, including the transsylvian, transcortical, and subtemporal approaches [4, 17]. There is no consensus regarding the preferability of the transsylvian or the transcortical approach for lesionectomy in the MTL.

In the transsylvian approach, the MTL structures are approached through the natural corridor, preserving the lateral temporal neocortex. The transcortical technique necessitates dissection of the lateral temporal neocortex. It can be performed through the superior, middle, or inferior temporal gyrus, with the trans-middle temporal gyrus (trans-MTG) approach being used in most instances [18–21].

Kowalczyk et al. [22] reported their experience with the trans-MTG approach to tumours of the MTL. They analyzed 14 children with MTL tumours, achieving gross-total resection (GTR) in all patients. Neurological deficits occurred in 21.4% of patients after surgery, with a concurrent 7.1% rate of visual field deficits. Notably, freedom from disabling seizures was reported to be 92.9%. Similarly, Lee et al. [17] reported that 91% of paediatric patients undergoing lesionectomy through the transsylvian approach were free from disabling seizures. Based on the results of their randomised trial, Lutz et al. [20] concluded that the trans-MTG approach provides better phonemic outcomes than the transsylvian approach, while cognitive outcomes and freedom from seizures were comparable between the two approaches. Based on their laboratory investigation, Bozkurt et al. [25] concluded that the trans-MTG approach may allow better visualisation of MTL structures than the transsylvian approach. Uda et al. [23] concluded that visual field deficits (83% vs. 60% respectively) and memory function were comparable between the trans-MTG approach and the transsylvian approach, with a shorter time of surgery for the trans-MTG approach. The typical trans-MTG approach, apart from damaging the lateral temporal neocortex, puts at risk some crucial white matter tracts (WMTs), such as inferior frontooccipital fasciculus (IFOF) and Meyer’s loop [24, 25].

On the other hand, it has been suggested that the transsylvian approach may be more selective, allowing for less interruption of WMTs (especially optic radiation fibres) and preservation of the lateral temporal neocortex [25]. It is worth remembering that it has been found that the transsylvian approach also interrupts IFOF, uncinate fasciculus (UF), and optic radiation fibres [24]. Moreover, some papers have indicated the presence of gliosis and neuronal loss in the temporal pole following the transsylvian approach [26, 27]. Recently, Shah et al. [24] proposed a modified technique for trans-MTG selective amygdalohippocampectomy that included a safe-entry zone in the anterior part of the lateral wall of the temporal horn. They suggested that a surgical approach focused on entering the temporal horn first, and then performing an en bloc resection of the amygdala, hippocampus, uncus, parahippocampus, and lateral neocortex, respectively, may preserve IFOF and Meyer’s loop fibres, making the trans-MTG approach safer. While this technique has been reported in a laboratory setting, further implementation in a clinical setting would be necessary to prove its superiority over the traditional trans-MTG approach.

Given that literature on the surgical strategies for lesional mTLE in children remains sparse, no strong evidence yet supports the superiority of one approach over another. Recent studies have found that both transsylvian and transcortical trough MTG approaches have their advantages and their disadvantages, and no consensus on the optimal surgical approach to MTL tumours exists. Both approaches can be considered equally effective, with comparable safety profiles. Visual field deficits constitute the limitations of both techniques, and these must be considered in the preoperative discussion with the patient’s caregivers.

Article information

Competing interests: On behalf of all authors, the corresponding author states that there is no conflict of interest.
Funding: No funding was received.
Supplementary material: None.

References

  1. Aaberg KM, Gunnes N, Bakken IJ, et al. Incidence and Prevalence of Childhood Epilepsy: A Nationwide Cohort Study. Pediatrics. 2017; 139(5), doi: 10.1542/peds.2016-3908, indexed in Pubmed: 28557750.
  2. Olusanya BO, Wright SM, Nair MKC, et al. Global Research on Developmental Disabilities Collaborators (GRDDC). Global Burden of Childhood Epilepsy, Intellectual Disability, and Sensory Impairments. Pediatrics. 2020; 146(1), doi: 10.1542/peds.2019-2623, indexed in Pubmed: 32554521.
  3. Sultana B, Panzini MA, Veilleux Carpentier A, et al. Incidence and Prevalence of Drug-Resistant Epilepsy: A Systematic Review and Meta-analysis. Neurology. 2021; 96(17): 805–817, doi: 10.1212/WNL.0000000000011839, indexed in Pubmed: 33722992.
  4. Chong S, Phi JiH, Lee JiY, et al. Surgical Treatment of Lesional Mesial Temporal Lobe Epilepsy. J Epilepsy Res. 2018; 8(1): 6–11, doi: 10.14581/jer.18002, indexed in Pubmed: 30090756.
  5. Asadi-Pooya AA, Nei M, Sharan A, et al. Historical Risk Factors Associated with Seizure Outcome After Surgery for Drug-Resistant Mesial Temporal Lobe Epilepsy. World Neurosurg. 2016; 89: 78–83, doi: 10.1016/j.wneu.2016.02.023, indexed in Pubmed: 26875655.
  6. Benifla M, Otsubo H, Ochi A, et al. Temporal lobe surgery for intractable epilepsy in children: an analysis of outcomes in 126 children. Neurosurgery. 2006; 59(6): 1203–13; discussion 1213, doi: 10.1227/01.NEU.0000245615.32226.83, indexed in Pubmed: 17277683.
  7. Sztriha L, Gururaj AK, Bener A, et al. Temporal lobe epilepsy in children: etiology in a cohort with new-onset seizures. Epilepsia. 2002; 43(1): 75–80, doi: 10.1046/j.1528-1157.2002.24201.x, indexed in Pubmed: 11879390.
  8. Dallas J, Englot DJ, Naftel RP. Neurosurgical approaches to pediatric epilepsy: Indications, techniques, and outcomes of common surgical procedures. Seizure. 2020; 77: 76–85, doi: 10.1016/j.seizure.2018.11.007, indexed in Pubmed: 30473268.
  9. Ormond DR, Clusmann H, Sassen R, et al. Pediatric Temporal Lobe Epilepsy Surgery in Bonn and Review of the Literature. Neurosurgery. 2019; 84(4): 844–856, doi: 10.1093/neuros/nyy125, indexed in Pubmed: 29668992.
  10. Elliott CA, Broad A, Narvacan K, et al. Seizure outcome in pediatric medically refractory temporal lobe epilepsy surgery: selective amygdalohippocampectomy versus anterior temporal lobectomy. J Neurosurg Pediatr. 2018; 22(3): 276–282, doi: 10.3171/2018.4.PEDS17607, indexed in Pubmed: 29932370.
  11. Benifla M, Rutka JT, Otsubo H, et al. Long-term seizure and social outcomes following temporal lobe surgery for intractable epilepsy during childhood. Epilepsy Res. 2008; 82(2-3): 133–138, doi: 10.1016/j.eplepsyres.2008.07.012, indexed in Pubmed: 18786810.
  12. Mittal S, Montes JL, Farmer JP, et al. Long-term outcome after surgical treatment of temporal lobe epilepsy in children. J Neurosurg. 2005; 103(5 Suppl): 401–412, doi: 10.3171/ped.2005.103.5.0401, indexed in Pubmed: 16302611.
  13. Barba C, Cossu M, Guerrini R, et al. TLE Study Group. Temporal lobe epilepsy surgery in children and adults: A multicenter study. Epilepsia. 2021; 62(1): 128–142, doi: 10.1111/epi.16772, indexed in Pubmed: 33258120.
  14. Barba C, Giometto S, Lucenteforte E, et al. Seizure Outcome of Temporal Lobe Epilepsy Surgery in Adults and Children: A Systematic Review and Meta-Analysis. Neurosurgery. 2022; 91(5): 676–683, doi: 10.1227/neu.0000000000002094, indexed in Pubmed: 35960753.
  15. Cataltepe O, Turanli G, Yalnizoglu D, et al. Surgical management of temporal lobe tumor-related epilepsy in children. J Neurosurg. 2005; 102(3 Suppl): 280–287, doi: 10.3171/ped.2005.102.3.0280, indexed in Pubmed: 15881751.
  16. Marathe K, Alim-Marvasti A, Dahele K, et al. Resective, Ablative and Radiosurgical Interventions for Drug Resistant Mesial Temporal Lobe Epilepsy: A Systematic Review and Meta-Analysis of Outcomes. Front Neurol. 2021; 12: 777845, doi: 10.3389/fneur.2021.777845, indexed in Pubmed: 34956057.
  17. Lee JiY, Phi JiH, Wang KC, et al. Transsylvian-transcisternal selective lesionectomy for pediatric lesional mesial temporal lobe epilepsy. Neurosurgery. 2011; 68(3): 582–587, doi: 10.1227/NEU.0b013e3182077552, indexed in Pubmed: 21164375.
  18. Mathon B, Clemenceau S. Selective amygdalohippocampectomy via trans-superior temporal gyrus keyhole approach. Acta Neurochir (Wien). 2016; 158(4): 785–789, doi: 10.1007/s00701-016-2717-4, indexed in Pubmed: 26852036.
  19. Uribe JS, Vale FL. Limited access inferior temporal gyrus approach to mesial basal temporal lobe tumors. J Neurosurg. 2009; 110(1): 137–146, doi: 10.3171/2008.4.17508, indexed in Pubmed: 18950264.
  20. Lutz MT, Clusmann H, Elger CE, et al. Neuropsychological outcome after selective amygdalohippocampectomy with transsylvian versus transcortical approach: a randomized prospective clinical trial of surgery for temporal lobe epilepsy. Epilepsia. 2004; 45(7): 809–816, doi: 10.1111/j.0013-9580.2004.54003.x, indexed in Pubmed: 15230706.
  21. Morshed RA, Young JS, Han SJ, et al. The transcortical equatorial approach for gliomas of the mesial temporal lobe: techniques and functional outcomes. J Neurosurg. 2019; 130(3): 822–830, doi: 10.3171/2017.10.JNS172055, indexed in Pubmed: 29676697.
  22. Kowalczyk P, Bobeff EJ, Nowak W, et al. Middle temporal gyrus approach to mesial temporal lobe tumours in children. Neurol Neurochir Pol. 2024; 58(3): 274–281, doi: 10.5603/pjnns.96409, indexed in Pubmed: 38393960.
  23. Uda H, Uda T, Tanoue Y, et al. Comparison of the keyhole trans-middle temporal gyrus approach and transsylvian approach for selective amygdalohippocampectomy: A single-center experience. J Clin Neurosci. 2020; 81: 390–396, doi: 10.1016/j.jocn.2020.10.019, indexed in Pubmed: 33222948.
  24. Shah A, Lunawat A, Jhawar SS, et al. White Fiber Correlates of Amygdalohippocampectomy Through the Middle Temporal Gyrus Approach. World Neurosurg. 2022; 157: e156–e165, doi: 10.1016/j.wneu.2021.09.116, indexed in Pubmed: 34619404.
  25. Faust K, Schmiedek P, Vajkoczy P. Approaches to temporal lobe lesions: a proposal for classification. Acta Neurochir (Wien). 2014; 156(2): 409–413, doi: 10.1007/s00701-013-1917-4, indexed in Pubmed: 24201756.
  26. Giacomini L, de Souza JP, Formentin C, et al. Temporal lobe structural evaluation after transsylvian selective amygdalohippocampectomy. Neurosurg Focus. 2020; 48(4): E14, doi: 10.3171/2020.1.FOCUS19937, indexed in Pubmed: 32234992.
  27. de Souza JP, Pimentel-Silva LR, Ayub G, et al. Transsylvian amygdalohippocampectomy for mesial temporal lobe epilepsy: Comparison of three different approaches. Epilepsia. 2021; 62(2): 439–449, doi: 10.1111/epi.16816, indexed in Pubmed: 33449366.