Bilateral Todd's paralysis in a patient with left fronto‐opercular epilepsy

Abstract

Postictal paresis (“Todd's paralysis”) is commonly observed as a unilateral, transient motor weakness, lasting minutes to hours, after focal or focal to bilateral tonic–clonic seizures, contralateral to the epileptogenic zone. Bilateral postictal paresis is exceedingly rare and could be misinterpreted, especially if the preceding convulsive phase was not witnessed. An 18‐year‐old right‐handed male patient with refractory focal epilepsy with seizure onset at age 3 years, was admitted for presurgical video‐EEG monitoring. His seizures were predominantly nocturnal, consisting of a laryngeal somatosensory aura, occasionally evolving to bilateral tonic or tonic–clonic seizures with occasional asymmetrical limb extension during the tonic phase (right arm extension). Postictally, consciousness recovery was fast, if ever lost. At that stage, we documented severe dysarthria and bilateral symmetrical arm paresis lasting several minutes. The ictal pattern and interictal epileptiform activity were projected on the fronto‐central midline. Brain MRI was highly suggestive of a bottom‐of‐sulcus dysplasia with underlying transmantle sign on the left premotor, fronto‐opercular region and an FDG‐PET‐CT showed a concordant left fronto‐operculo‐insular hypometabolism. A complete lesionectomy was performed, with the additional guidance of intraoperative electrocorticography, resulting in sustained seizure freedom. Anatomo‐pathology confirmed a type 2b focal cortical dysplasia. We speculate that, in our patient, a left fronto‐opercular ictal onset with an early spread to both primary motor cortices and relative sparing of consciousness networks allowed the emergence of a clinically detectable postictal bilateral paresis.