New onset refractory status epilepticus (NORSE) is a heterogeneous condition that results in super RSE (SRSE) requiring multiple therapeutic doses of antiseizure medications, anesthetic coma, prolonged intensive care unit (ICU) stays, immunomodulation, dietary therapies, and epilepsy surgeries [1]. Medical management alone is generally insufficient for seizure freedom [1]. NORSE often remains etiologically elusive despite extensive workup for infectious, structural, metabolic, paraneoplastic, autoimmune, and genetic causes [1]. Respiratory complications during mechanical ventilation result in 50% of deaths [1, 2]. Surgery is considered when epilepsy is drug-resistant, defined as failure of therapeutic doses of two anticonvulsant medications with unique mechanisms [2, 3]. The ideal surgical candidate has a focal epileptogenic zone (EZ) amenable to resection or stereotactic thermal ablation [4]. Lateralizing the EZ in frontal lobe epilepsy is challenging due to secondary bilateral synchrony from commissural connections through the corpus callosum and low spatiotemporal resolution of the scalp electroencephalography (EEG) [4]. Stereo-EEG (sEEG) can lateralize and localize the EZ, though bilateral homologous ictal patterns are seen [4]. Corpus callosotomy (CC) lateralized an EZ in frontal lobe epilepsy in an adult patient with atonic seizures when bilateral ictal patterns on sEEG were encountered [5]. Both CC and magnetic resonance-guided laser interstitial thermal therapy (MRgLITT) CC are therapeutic for tonic and atonic seizures with fall injuries in pediatric patients and have lateralized interictal discharges as well [6, 7]. We report a pediatric patient with NORSE presenting with focal impaired awareness seizures clustering into SRSE requiring definitive surgical intervention for treatment of her seizures following therapeutic doses of anticonvulsant medications, anesthetic drips, immunomodulation, and an adequate trial of the ketogenic diet. The seizures were not all lateralized during phase 2 sEEG. Anterior MRgLITT CC was performed in a multistage surgical approach to successfully lateralize the EZ after a bilateral ictal pattern was seen on scalp EEG and phase 2 sEEG.

A 5-year-old, right-handed girl presented with new onset status epilepticus with frequent focal impaired awareness seizures without return to baseline. She did not have a fever or intercurrent illness. Her semiology was waking up with “nightmares”, drooling with the elevation of the right arm, hyperkinetic leg scissoring, and gaze deviation to the right. Her examination was nonfocal, and she had altered mental status due to frequent seizures and did not follow commands. Her seizures were captured with prolonged EEG which showed a non-lateralizing ictal pattern with fast activity seen predominantly in the bifrontal head regions (Figure 1). She had drug-resistant epilepsy, requiring intravenous (IV) loads of levetiracetam 60 mg/kg IV, fosphenytoin 20 mgPE/kg IV, valproate sodium 40 mg/kg IV, and lacosamide 10 mg/kg IV along with trials of oral maintenance oxcarbazepine, clobazam, topiramate, and cannabidiol. Immunomodulation with a pulse dose of 30 mg/kg per day IV methylprednisolone for 5 days, an infusion of 2 gm/kg IV immunoglobulin (IVIG), and a trial of anakinra 100 mg/day subcutaneously for 5 days were unsuccessful. The ketogenic diet did not significantly improve her seizures over 1 month. She had SRSE and required anesthetic coma with burst suppression for seizure reduction utilizing midazolam, ketamine, and pentobarbital drips without complete seizure freedom. Seizures recurred frequently at 1–5 per hour with weaning of the drips. She remained in the ICU intubated and sedated. Complete blood count, complete metabolic panel, lactate, pyruvate, ammonia, and metabolic testing with free and total carnitine, acylcarnitine profile, plasma amino acids, urine amino acids, and urine organic acids were unrevealing. Lumbar puncture was normal with cell count of 3/mm³ (reference 0–5), glucose of 61 mg/dL (reference 40–70), protein of 13 mg/dL (reference 15–45), and negative culture and stain. Other infectious workups included Epstein-Barr virus, West Nile virus, St. Louis Encephalitis virus, California Encephalitis virus, Eastern Encephalitis virus, and Western Encephalitis virus titers which were unremarkable. The autoimmune and paraneoplastic encephalitis panel sent to the Mayo Clinic was negative [8]. Mitochondrial genome testing was negative, and whole exome sequencing revealed a heterozygous variant of unknown significance in the HIVEP2 gene which was determined to be non-pathogenic and shared by her asymptomatic father.

A phase 1 workup for epilepsy surgery was performed while she was intubated and sedated in the ICU. Magnetic resonance imaging (MRI) of the brain without and with gadolinium contrast showed mild cerebral volume loss, and magnetic resonance spectroscopy was normal. Whole body positron emission tomography-computed tomography (PET/CT) was negative, and interictal PET/CT of the brain showed no hypometabolic focus, though this was suspected to be falsely negative due to frequent seizures. Ictal single photon emission CT (SPECT) revealed left hemispheric perfusion in the left occipital lobe, left parietal lobe, and left thalamus. Interictal SPECT was performed for subtracted ictal SPECT co-registered to MRI (SISCOM) which was also nondiagnostic though the Interictal SPECT was likely impacted due to frequent seizures. Following the discussion in the Comprehensive Epilepsy Program Conference at Riley Hospital for Children, she was hypothesized to have frontal lobe epilepsy, though her phase 1 workup was inconclusive for the laterality of her EZ. Due to her ictal SPECT having a wide region of hyperperfusion, sEEG was performed with a wide coverage of her bilateral frontal, temporal, and insular lobes.

A phase 2 workup in the ICU while intubated and sedated with sEEG revealed multifocal onset seizures with the left inferior frontal contacts, the left anterior insular contacts, and a bilateral ictal pattern involving the orbitofrontal contacts (Figure 2). The left inferior frontal contacts were hypothesized to be proximal to the eloquent language cortex given that she was right-handed so no ablation or resection could be performed in that region. Furthermore, cortical mapping of the left inferior frontal sEEG contacts could not be performed due to her being intubated and sedated. The left anterior insular contacts and rostrum, genu, and body of the CC were ablated utilizing MRgLITT (Figure 3). Reimplantation of sEEG revealed that the bilateral orbitofrontal ictal pattern lateralized to the left at onset following MRgLITT CC (Figure 4). Due to her seizures being focal impaired awareness seizures, MRgLITT CC did not appreciably reduce the number of seizures. MRgLITT of the left anterior insular contacts eliminated seizures from this region, confirmed by the electrocorticography measured by reimplantation of depth electrodes.

NORSE is a devastating, heterogeneous, drug-resistant epilepsy with status epilepticus refractory to conventional antiseizure medications, without structural or metabolic cause on imaging and laboratory studies, and with or without intercurrent illness or fever [1, 9]. Drug-resistant epilepsy is defined as the failure of two or more antiseizure medications for efficacy [9, 10]. Once a patient is determined to have drug-resistant epilepsy, treatments may continue with trials of additional antiseizure medications, though medical management is unlikely to result in seizure freedom even with newer-generation antiseizure medications [10]. The ketogenic diet and immunomodulation are often effective treatments in NORSE, though a broad workup should be performed to diagnose an underlying cause for guiding therapy [1, 9].

Identifying the EZ in patients with focal epilepsy is critical for definitive surgical intervention if medical, immunomodulatory, and dietary management fail [2–4]. If a lateralized EZ is not identified during phase 1 testing, patients may have staged a surgical intervention with a phase 2 evaluation and can be further studied after CC if bilateral interictal or ictal patterns are seen on sEEG [5–7, 10, 11].

The EZ is the smallest cortical region generating focal epileptic seizures [10]. Resection or ablation of the EZ leads to seizure freedom [10, 12]. An extensive network of connections afforded by the commissural fibers of the corpus callosum allows for rapid ictal spread which clinically manifests with diverse semiologies [5, 11, 13]. Bilateral homologous ictal patterns are often seen on non-invasive scalp EEG and with sEEG [5, 10, 11]. We report the case of a 5-year-old female found to have a bilateral homologous ictal pattern on sEEG which was successfully lateralized following MRgLITT CC.

Previous authors have described CC and MRgLITT CC as a palliative procedure to reduce atonic and tonic seizures, fall injuries, and epileptic encephalopathy [14–17]. Greiner et al. [14] 2012 reported a 9-year-old boy with drug-resistant epilepsy was treated with CC to prevent relapse into RSE. CC has previously lateralized interictal discharges which appeared bilateral on scalp EEG [7]. These bilateral discharges could be misinterpreted as generalized discharges, though if a lateralized EZ is suspected, discharges could be lateralized interictal discharges and determined to be focal following CC [7]. Truong et al. [5] 2014 described anterior CC successfully lateralizing the EZ in an 18-year-old female with atonic seizures and bilateral synchronous ictal activity in the supplemental motor area following sEEG implantation. Once the EZ is lateralized and localized, RSE can be treated with focal resection or ablation, and CC can be used in multistage epilepsy surgery for children with drug-resistant epilepsy [18, 19]. In a retrospective study of 10 patients with a focal EZ and presenting with RSE, all were treated surgically and without mortality [20].

The CC can be complete or focused to the anterior two-thirds and with an open technique following craniotomy or performed with minimally invasive MRgLITT [5, 6, 15]. Technique selection and extent of CC are based on patient age, baseline neurocognitive status, and surgeon preference [15]. Dallas et al. [15] reported that pediatric patients are better served by complete callosotomy owing to better rates of seizure control if patients have low neurocognitive status prior to surgery. A recent meta-analysis showed complete seizure freedom at a rate of 18.8% [21]. Parental satisfaction is seen in most cases secondary to functional improvements and seizure reduction [22].

While generally well tolerated, CC can result in disconnection syndromes which occur due to failure to transfer unilateral stimuli through the brain [23]. Other possible complications of CC include hemorrhage and infection, though these are rare. Disconnection syndromes following CC include supplementary motor area syndrome, hemispatial neglect, astereognosis, or alexia without agraphia, though these deficits are often transient and minimized by performing only a partial CC [23].

Epilepsy surgery should be considered in patients with focal drug-resistant epilepsy or NORSE with SRSE after the failure of medical management, defined as a trial of two antiseizure medications of appropriate mechanisms that do not result in seizure freedom and if no reversible cause of seizures is found [2, 3, 24]. We describe a case of NORSE with SRSE in a child with a challenging bilateral ictal pattern on scalp EEG and sEEG, with MRgLITT CC successfully lateralizing the EZ.