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Updated: Jan 19, 2026

Network Analysis of Foramen Ovale Electrode Recordings in Drug-resistant Temporal Lobe Epilepsy Patients
Published on: December 18, 2016
Drug Refractory Epilepsy - A Series of Lesions with Triple Pathology
Vivek Tandon1, Poodepedi Sarat Chandra1, Raghav Singla1
1Department of Neurosurgery, Cardioneurosciences Centre, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.
Abstract:
The associations between gangliogliomas, dysembryoplastic neuroepithelial tumors (DNETs), and cortical dysplasias remain debatable. We report five cases of drug refractory epilepsy with temporal lobe lesions. On resection, histopathological examination showed distinctive areas of gangliogliomas and DNETs with cortical dysplasia. The coexistence of the above three lesions as distinct entities in a single lesion is virtually unknown. This points to the presence of a possible etiological relationship among them. Finally, we also delve into a plausible hypothesis for such a pathogenesis.
Insights
Gangliogliomas, dysembryoplastic neuroepithelial tumors (DNETs), and cortical dysplasia may share an etiological link. This study presents rare cases of coexisting lesions, suggesting a common pathogenesis in drug-refractory epilepsy.
Area of Science:
- Neuro-oncology
- Epileptology
- Neuropathology
Background:
- The relationship between gangliogliomas, dysembryoplastic neuroepithelial tumors (DNETs), and cortical dysplasia is not well-established.
- These entities are common causes of drug-refractory epilepsy, particularly in the temporal lobe.
Observation:
- This study details five cases of patients with drug-refractory epilepsy and temporal lobe lesions.
- Histopathological examination of resected lesions revealed distinct areas of gangliogliomas, DNETs, and cortical dysplasia within the same specimen.
Findings:
- The simultaneous occurrence of gangliogliomas, DNETs, and cortical dysplasia as distinct components within a single lesion is exceptionally rare.
- This unique coexistence suggests a potential shared etiology or developmental pathway among these pathologies.
Implications:
- The findings challenge current classifications and highlight a possible etiological relationship between these tumor types and cortical malformations.
- Further research into the pathogenesis of these coexisting lesions may offer new insights into the development of epilepsy and guide therapeutic strategies.
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