Javascript must be enabled to continue!
Absence seizures in lesion-related epilepsy
View through CrossRef
Abstract
Background
In the new International League Against Epilepsy (ILAE) classification of seizure types, generalized seizures such as absence seizures (ASs) may originate from a focal point and rapidly spread to the bilaterally distributed brain network. Increasing evidence from animal and clinical studies has indicated that focal changes may occur prior to ASs; however, the relationship of ASs with epileptogenic lesions remains unclear.
Methods
We retrospectively collected and analyzed the clinical, imaging, and electrophysiological data of 16 patients who had ASs and structural lesions with seizure-free outcomes after lesion resection.
Results
In semiology analysis, nine patients displayed focal onset; only two patients showed simple ASs, and seizure types other than ASs were observed in the remaining patients. On ictal electroencephalography (EEG), four patients showed bilateral synchronous symmetric 3 Hz generalized spike-wave discharges (GSWDs), and the remaining patients showed bilateral 1.5–2.5 Hz GSWDs. Moreover, most patients (13/16, 81.3%) exhibited focal features in addition to ASs, while interictal EEG was the same in 12 patients. Furthermore, on stereoelectroencephalogram (SEEG), 2/5 patients showed focal discharges before bilateral burst GSWDs. Additionally, all patients had structural lesions on imaging. In four typical AS patients, the lesions were located in deep brain regions. Notably, in 9 patients (9/16, 56%), the lesions were located in the posterior cortex. All patients underwent lesion resection and had seizure-free outcomes during follow-up, and intelligence quotient (IQ) also improved by 10.71 ± 3.90 one year after surgery.
Conclusions
Patients with lesion-related epilepsy may present with ASs that have a focal onset and are associated with good surgical outcomes.
Springer Science and Business Media LLC
Title: Absence seizures in lesion-related epilepsy
Description:
Abstract
Background
In the new International League Against Epilepsy (ILAE) classification of seizure types, generalized seizures such as absence seizures (ASs) may originate from a focal point and rapidly spread to the bilaterally distributed brain network.
Increasing evidence from animal and clinical studies has indicated that focal changes may occur prior to ASs; however, the relationship of ASs with epileptogenic lesions remains unclear.
Methods
We retrospectively collected and analyzed the clinical, imaging, and electrophysiological data of 16 patients who had ASs and structural lesions with seizure-free outcomes after lesion resection.
Results
In semiology analysis, nine patients displayed focal onset; only two patients showed simple ASs, and seizure types other than ASs were observed in the remaining patients.
On ictal electroencephalography (EEG), four patients showed bilateral synchronous symmetric 3 Hz generalized spike-wave discharges (GSWDs), and the remaining patients showed bilateral 1.
5–2.
5 Hz GSWDs.
Moreover, most patients (13/16, 81.
3%) exhibited focal features in addition to ASs, while interictal EEG was the same in 12 patients.
Furthermore, on stereoelectroencephalogram (SEEG), 2/5 patients showed focal discharges before bilateral burst GSWDs.
Additionally, all patients had structural lesions on imaging.
In four typical AS patients, the lesions were located in deep brain regions.
Notably, in 9 patients (9/16, 56%), the lesions were located in the posterior cortex.
All patients underwent lesion resection and had seizure-free outcomes during follow-up, and intelligence quotient (IQ) also improved by 10.
71 ± 3.
90 one year after surgery.
Conclusions
Patients with lesion-related epilepsy may present with ASs that have a focal onset and are associated with good surgical outcomes.
Related Results
Portrait of Epilepsy on the Canvas of Global Health
Portrait of Epilepsy on the Canvas of Global Health
Global, regional, and national burden of epilepsy, 1990-2021: a systematic analysis for the Global Burden of Disease Study 2021.
GBD Epilepsy Collabora...
Seizures in Rural Zambia
Seizures in Rural Zambia
Summary: Purpose: To describe the period prevalence of epilepsy and febrile seizures in a bush hospital and discuss the medical sequelae and social impact of seizures in this pop...
Epilepsy in children and anesthesia
Epilepsy in children and anesthesia
Epilepsy, also called seizure disorder, is the most common childhood brain disorder in the United States. The aetiology of epilepsy in children is multifactorial with congenital, m...
Prediction of Seizures in Patients with Temporal Lobe Epilepsy, more than 30 minutes before onset
Prediction of Seizures in Patients with Temporal Lobe Epilepsy, more than 30 minutes before onset
Dear Madam,
Around 52.5 million people worldwide suffer from the neurological illness known as epilepsy, which is frequently characterized by recurring seizures. (1, 2) As epilepsy...
Automatic Responsiveness Testing in Epilepsy with Wearable Technology: The ARTiE Watch
Automatic Responsiveness Testing in Epilepsy with Wearable Technology: The ARTiE Watch
AbstractObjectiveAn accurate evaluation of behavioral responsiveness during and after seizures in people with epilepsy is critical for accurate diagnosis and management. Current me...
Advancements in Epilepsy Treatment: Challenges, Innovations, and Social Impacts on Patients
Advancements in Epilepsy Treatment: Challenges, Innovations, and Social Impacts on Patients
Epilepsy-related seizures can range greatly, from focal seizures that can impact certain brain areas to widespread tonic-clonic seizures. Although the exact origin of epilepsy is s...
River Epilepsy—A Preventable Form of Epilepsy
River Epilepsy—A Preventable Form of Epilepsy
Effect of Onchocerciasis Elimination Measures on the Incidence of Epilepsy in Maridi, South Sudan: A 3-Year Longitudinal, Prospective, Population-Based Study.
...
Myoclonic‐Astatir Epilepsy: A Report of Three Intractable Cases.
Myoclonic‐Astatir Epilepsy: A Report of Three Intractable Cases.
Purpose: Myoclonic‐astatic epilepsy (MAE), as first described by Doose (1970), is a rare generalized epilepsy of early childhood characterized by myoclonic, astatic, and myoclonic‐...

