<scp>ILAE</scp> neuroimaging task force highlight: Tuberous sclerosis complex‐related epilepsy

The ILAE Neuroimaging Task Force publishes educational case reports that highlight basic aspects of neuroimaging in epilepsy consistent with the ILAE's educational mission. Tuberous sclerosis complex (TSC) is a rare, complex, and multisystem autosomal dominant genetic disorder that arises from variations in the TSC1 or TSC2 genes. While characterized by a wide range of clinical manifestations, TSC commonly presents with epilepsy, which is a clinically challenging feature of the condition. Neuroimaging plays a pivotal role in the early diagnosis, screening, and long-term monitoring of TSC patients. CT serves as the first-line imaging tool in emergency settings; yet MRI is the primary diagnostic modality for TSC. In this report, we present two patients with TSC-related epilepsy and analyze their neuroimaging findings. We also address the diagnostic and therapeutic challenges faced by TSC patients with epilepsy.

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Publication Details

Journal
Epileptic Disorders
Published
2025-08-18
DOI
https://doi.org/10.1002/epd2.70087
Primary Topic
Tuberous Sclerosis Complex Research
Type
article
Field-Weighted Citation Impact
0.00

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article

ILAE neuroimaging task force highlight: Tuberous sclerosis complex‐related epilepsy

Boris C. Bernhardt, Irène Wang, Stefan Rampp, Lorenzo Caciagli et al.
1 links
Epileptic Disorders
Tuberous Sclerosis Complex Research
article

ILAE neuroimaging task force highlight: Tuberous sclerosis complex‐related epilepsy

Boris C. Bernhardt, Irène Wang, Stefan Rampp, Lorenzo Caciagli, Paolo Federico, Shuang Wang, Eliane Kobayashi, John S. Archer, Gavin P. Winston, William D. Gaillard, Anna Elisabetta Vaudano, Fernando Cendes, Yotin Chinvarun, Luis Concha, Godwin Inalegwu Ogbole, Xiao Chen
article en

Abstract

The ILAE Neuroimaging Task Force publishes educational case reports that highlight basic aspects of neuroimaging in epilepsy consistent with the ILAE's educational mission. Tuberous sclerosis complex (TSC) is a rare, complex, and multisystem autosomal dominant genetic disorder that arises from variations in the TSC1 or TSC2 genes. While characterized by a wide range of clinical manifestations, TSC commonly presents with epilepsy, which is a clinically challenging feature of the condition. Neuroimaging plays a pivotal role in the early diagnosis, screening, and long-term monitoring of TSC patients. CT serves as the first-line imaging tool in emergency settings; yet MRI is the primary diagnostic modality for TSC. In this report, we present two patients with TSC-related epilepsy and analyze their neuroimaging findings. We also address the diagnostic and therapeutic challenges faced by TSC patients with epilepsy.

Epileptic DisordersVol. 27(6)
University of Modena and Reggio Emilia (IT), George Washington University Hospital (US), Montreal Neurological Institute and Hospital (CA), Cleveland Clinic (US), University of Calgary (CA), Universidade Estadual de Campinas (UNICAMP) (BR), University of Ibadan (NG), Queen's University (CA), University Hospital of Bern (CH), Phramongkutklao Hospital (TH), Universitätsklinikum Erlangen (DE), Southwestern Medical Center (US), Second Affiliated Hospital of Zhejiang University (CN), Austin Health (AU), Hotchkiss Brain Institute (CA), McGill University (CA), The University of Texas Southwestern Medical Center (US), Universidad Nacional Autónoma de México (MX)
National Natural Science Foundation of China, Natural Science Foundation of Zhejiang Province
Good health and well-being
Openalex Percentile: Top 73%
Tuberous Sclerosis Complex Research
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