Temporal encephaloceles and coexisting epileptogenic lesions.


Journal

Epilepsia open
ISSN: 2470-9239
Titre abrégé: Epilepsia Open
Pays: United States
ID NLM: 101692036

Informations de publication

Date de publication:
03 2023
Historique:
received: 31 08 2022
accepted: 18 11 2022
pubmed: 22 11 2022
medline: 4 3 2023
entrez: 21 11 2022
Statut: ppublish

Résumé

This study was performed to identify coexisting structural lesions in patients with epilepsy and known temporal encephaloceles (TEs). Forty-seven structural magnetic resonance imaging (MRI) scans of patients with epilepsy and radiologically diagnosed TEs were retrospectively reviewed visually and using an automated postprocessing software, the Morphometric Analysis Program v2018 (MAP18), to depict additional subtle, potentially epileptogenic lesions in the 3D T1-weighted MRI data. All imaging findings were evaluated in the context of clinical and electroencephalographical findings. The study population consisted of 47 epilepsy patients (38.3% female, n = 18). The median age at the time of the scan was 40 years (range 12-81 years). Twenty-one out of 47 MRI scans (44.7%) showed coexisting lesions in the initial MRI evaluation; in 38.3% (n = 18) of patients, those lesions were considered probably epileptogenic. After postprocessing, probable epileptogenic lesions were identified in 53.2% (n = 25) of patients. Malformations of cortical development had initially been reported in 17.0% (n = 8) of patients with TEs, which increased to 38.3% (n = 18) after postprocessing. TEs and other epileptogenic lesions were considered equally epileptogenic in 21.3% (n = 10) of the cases in the initial MR reports and 25.5% (n = 12) of the cases after postprocessing. Temporal encephaloceles are a potential cause of MRI-negative temporal lobe epilepsy. According to our data, TEs can occur with other lesions, suggesting that increased awareness is also required in patients with lesional epilepsy. TEs may not always be epileptogenic; hence, their occurrence with other structural pathologies may influence the presurgical evaluation and surgical approach. Finally, TEs can be associated with malformations of cortical development, which may indicate a common developmental etiology of those lesions.

Identifiants

pubmed: 36408781
doi: 10.1002/epi4.12674
pmc: PMC9977755
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

113-124

Informations de copyright

© 2022 The Authors. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy.

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Auteurs

Panagiota-Eleni Tsalouchidou (PE)

Epilepsy Center Hessen, Department of Neurology, Philipps University Marburg, Marburg, Germany.

Johann Philipp Zoellner (JP)

Epilepsy Center Frankfurt Rhine-Main and Department of Neurology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Center for Personalized Translational Epilepsy Research (CePTER), Goethe University Frankfurt, Frankfurt, Germany.

Annika Kirscht (A)

Epilepsy Center Frankfurt Rhine-Main and Department of Neurology, Goethe University Frankfurt, Frankfurt am Main, Germany.

Christina Julia Mueller (CJ)

Epilepsy Center Hessen, Department of Neurology, Philipps University Marburg, Marburg, Germany.

Christopher Nimsky (C)

Department of Neurosurgery, Philipps University Marburg, Marburg, Germany.

Maximilian Schulze (M)

Division of Neuroradiology, Philipps University Marburg, Marburg, Germany.

Elke Hattingen (E)

Center for Personalized Translational Epilepsy Research (CePTER), Goethe University Frankfurt, Frankfurt, Germany.
Department of Neuroradiology, Goethe University, Frankfurt, Germany.

Georgios Chatzis (G)

Department of Cardiology, Angiology and Intensive Care, Philipps University Marburg, Marburg, Germany.

Thomas M Freiman (TM)

University Medical Center Rostock, Rostock, Germany.

Adam Strzelczyk (A)

Epilepsy Center Frankfurt Rhine-Main and Department of Neurology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Center for Personalized Translational Epilepsy Research (CePTER), Goethe University Frankfurt, Frankfurt, Germany.

Sven Fuest (S)

Epilepsy Center Hessen, Department of Neurology, Philipps University Marburg, Marburg, Germany.

Katja Menzler (K)

Epilepsy Center Hessen, Department of Neurology, Philipps University Marburg, Marburg, Germany.
Center for Mind, Brain and Behavior (CMBB), Philipps-University Marburg, Marburg, Germany.
Core Facility Brainimaging, Faculty of Medicine, University of Marburg, Marburg, Germany.

Felix Rosenow (F)

Epilepsy Center Frankfurt Rhine-Main and Department of Neurology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Center for Personalized Translational Epilepsy Research (CePTER), Goethe University Frankfurt, Frankfurt, Germany.

Susanne Knake (S)

Epilepsy Center Hessen, Department of Neurology, Philipps University Marburg, Marburg, Germany.
Center for Personalized Translational Epilepsy Research (CePTER), Goethe University Frankfurt, Frankfurt, Germany.
Center for Mind, Brain and Behavior (CMBB), Philipps-University Marburg, Marburg, Germany.
Core Facility Brainimaging, Faculty of Medicine, University of Marburg, Marburg, Germany.

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Classifications MeSH