Objective: To determine clinical and EEG features that might help identify patients with epilepsy harboring small, intrinsically epileptogenic, surgically treatable, bottom-of-sulcus dysplasias (BOSDs).Methods: Retrospective review of clinical records, EEG, MRI, and histopathology in 32 patients with drug-resistant epilepsy and MRI-positive (72% 3.0 tesla), pathologically proven (type 2B cortical dysplasia) BOSDs operated at our centers during 2005-2013. Results: Localization of BOSDs was frontal in 19, insula in 5, parietal in 5, and temporal in 3, on the convexity or interhemispheric surfaces. BOSDs were missed on initial MRI at our centers in 22% of patients. Patients presented with focal seizures during infancy in 9, preschool years in 15, and school years in 8 (median age 5 years). Seizures were stereotyped, predominantly nocturnal, and typically nonconvulsive, with semiology referable to the fronto-central or perisylvian regions. Seizures occurred at high frequency during active periods, but often went into prolonged remission with carbamazepine or phenytoin. Intellect was normal or borderline, except in patients with seizure onset during infancy. Scalp EEG frequently revealed localized interictal epileptiform discharges and ictal rhythms. Patients underwent lesionectomy (median age 14 years) guided by electrocorticography and MRI, with prior intracranial EEG monitoring in only one patient. Twentyeight patients (88%) became seizure-free, and 20 discontinued antiepileptic medication (median follow-up 4.1 years).
Conclusions:In patients with cryptogenic focal epilepsy, this clinical presentation and course should prompt review of or repeat MRI, looking for a BOSD in the frontal, parietal, or insula cortex. If a BOSD is identified, the patient might be considered for single-stage lesionectomy.
Bottom-of-sulcus dysplasia (BOSD)1 is a localized variety of type 2 focal cortical dysplasia (FCD) in which the dysplastic features are maximal at the sulcal depth, tapering to a relatively normal gyral crown.2,3 Pathologically, BOSDs are characterized by neuronal dyslamination and dysmorphology, with or without balloon cells, at the bottom of the sulcus, with hypomyelination in the underlying white matter. 2,4,5 The characteristic MRI features of BOSD are cortical thickening, gray-white junction blurring, and subcortical T2 hyperintensity, often tapering to the ventricle as a "transmantle sign." [6][7][8][9] Straightening and elongation of the dysplastic sulcus, and depression or unusual sulcation of the overlying cerebral surface, may also be appreciated. 8,10,11 BOSDs are typically found in the frontal and parietal lobes.