Vigabatrin efficacy in focal cortical dysplasia type II with refractory focal status epilepticus, suspected role of mTOR inhibition
Focal cortical dysplasia (FCD) type II is a group of malformation of cortical development (MCD) which is the result of abnormal proliferation in the brain. Nowadays, FCD II is classified as mTORopathies caused by mutations leading to abnormal hyperactivation of the mTOR pathway. It locates in the same subcategory as hemimegalencephaly (HME) and tuberous sclerosis complex (TSC). We describe a child with refractory focal status epilepticus and brain MRI features of FCD type II, who did not respond to the usual anti-seizure medications (ASMs) but showed a dramatic response after initiation of vigabatrin. Vigabatrin is an anti-seizure medication with a high response rate for the treatment of infantile spasms and refractory focal epilepsy in TSC. We concluded that vigabatrin could be a promising precision therapy for refractory epilepsy of FCD type II, which has the same pathologic and molecular abnormalities as TSC. • FCD II is classified as mTORopathies in the same group as tuberous sclerosis complex (TSC). • MTORopathies are caused by mutations leading to abnormal hyperactivation of the mTOR pathway. • Most FCD II are distinguishable in brain MRI based on specific features like cortical thickness changes and transmantle sign. • Vigabatrin showed decreased activation of the mTOR pathway in animal models. • Vigabatrin could be a promising precision therapy in refractory epilepsy due to FCD II.
Authors
- Reza Kaboodkhani (ORCID: https://orcid.org/0000-0002-2754-2884)
- Safoura Kowkabi (ORCID: https://orcid.org/0000-0001-6508-9913)
- Zahra Rezaei (ORCID: https://orcid.org/0000-0001-5912-6175)
- Parvin Ghaemmaghami
- Mohammad Kaboodkhani
Institutions
- Shiraz University of Medical Sciences (IR)
- Tehran University of Medical Sciences (IR)
Publication Details
- Journal
- Brain and Development Case Reports
- Published
- 2024-12-13
- DOI
- https://doi.org/10.1016/j.bdcasr.2024.100055
- Primary Topic
- Mitochondrial Function and Pathology
- Type
- article
- Field-Weighted Citation Impact
- 0.00