First corpus callosotomy for medically refractory epilepsy in The Gambia: an international cooperation case report and historical review

BACKGROUND: Epilepsy affects over 50 million people worldwide, with the majority residing in low- and middle-income countries (LMICs) where access to specialized care is often constrained. Surgical intervention represents a crucial therapeutic modality for patients with medically refractory epilepsy, yet epilepsy surgery remains markedly underutilized in sub-Saharan Africa. CASE PRESENTATION: We report the case of a 10-year-old boy in The Gambia with medically refractory epilepsy characterized by daily drop attacks. Despite optimized and adequately trialed therapy with carbamazepine and sodium valproate, he continued to experience disabling seizures, leading to recurrent head trauma. Computed tomography (CT) and magnetic resonance imaging (MRI) did not reveal an identifiable structural lesion. Given the intractability of seizures and significant associated morbidity, he underwent a corpus callosotomy. The procedure was performed via a standard microsurgical approach and concurrently addressed the resection of traumatic calcified scalp hematomas. The patient's postoperative recovery was uneventful, and he was discharged on postoperative day 13 and remained seizure-free. At the six-month postoperative follow-up, the patient achieved complete freedom from drop attacks, with generalized tonic-clonic seizures (GTCS) occurring only during periods of antiseizure medication (ASM) interruption. CONCLUSIONS: This case highlights the feasibility and therapeutic potential of epilepsy surgery in the context of a surgical program within a resource-limited setting. Scaling up access to epilepsy surgery in comparable environments could contribute to mitigating the global epilepsy treatment gap.

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Publication Details

Journal
Acta Epileptologica
Published
2026-05-31
DOI
https://doi.org/10.1186/s42494-026-00258-2
Primary Topic
Epilepsy research and treatment
Type
article
Field-Weighted Citation Impact
0.00
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article

First corpus callosotomy for medically refractory epilepsy in The Gambia: an international cooperation case report and historical review

Pokua Sarpong, Nantenin Doumbia, Fatoumata Jallow, Gabrielle Luiselli et al.
Acta Epileptologica
Epilepsy research and treatment
article

First corpus callosotomy for medically refractory epilepsy in The Gambia: an international cooperation case report and historical review

Pokua Sarpong, Nantenin Doumbia, Fatoumata Jallow, Gabrielle Luiselli, Lamin Janneh, Maguette Mbaye, Sabina Kangakan, Ancha Ceesay, Makumba Cham, Mariam Joof, Saksham Gupta, Oley Bojang, Adama Njie, Yohana C. Sanchez, Musa Barry, Malick Jammeh, Mustapha Bittaye, Mhd A. Alkhateeb, Richard Oguocha, John N. Jabang, Mai Nyassi, Tida Jagne, Kebba S. Marenah, Yusupha Jobe, Zsombor T. Gal, Ebrima K. Manneh, Mary F. Gomez, Eduardo R. Cobas, John D. Rolston, Cherno S. Jallow
article en

Abstract

BACKGROUND: Epilepsy affects over 50 million people worldwide, with the majority residing in low- and middle-income countries (LMICs) where access to specialized care is often constrained. Surgical intervention represents a crucial therapeutic modality for patients with medically refractory epilepsy, yet epilepsy surgery remains markedly underutilized in sub-Saharan Africa. CASE PRESENTATION: We report the case of a 10-year-old boy in The Gambia with medically refractory epilepsy characterized by daily drop attacks. Despite optimized and adequately trialed therapy with carbamazepine and sodium valproate, he continued to experience disabling seizures, leading to recurrent head trauma. Computed tomography (CT) and magnetic resonance imaging (MRI) did not reveal an identifiable structural lesion. Given the intractability of seizures and significant associated morbidity, he underwent a corpus callosotomy. The procedure was performed via a standard microsurgical approach and concurrently addressed the resection of traumatic calcified scalp hematomas. The patient's postoperative recovery was uneventful, and he was discharged on postoperative day 13 and remained seizure-free. At the six-month postoperative follow-up, the patient achieved complete freedom from drop attacks, with generalized tonic-clonic seizures (GTCS) occurring only during periods of antiseizure medication (ASM) interruption. CONCLUSIONS: This case highlights the feasibility and therapeutic potential of epilepsy surgery in the context of a surgical program within a resource-limited setting. Scaling up access to epilepsy surgery in comparable environments could contribute to mitigating the global epilepsy treatment gap.

Acta EpileptologicaVol. 8(1)
Edward Francis Small Teaching Hospital (GM), Massachusetts General Hospital (US), Centre Hospitalier National Universitaire de Fann (SN)
Partnerships for the goals
Openalex Percentile: Top 6%
Epilepsy research and treatment
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