Hyperkinetic Manifestation in a Patient with Hippocampal Atrophy

Describes a case of a patient that presents with hippocampal atrophy leading to hyperkinetic crises of parietal-occipital origin. Citation: Almeida RD, Regino JSP, Costa TDA, Ortiz AEC, Resende LPD, et al. (2017) Hyperkinetic Manifestation in a Patient with Hippocampal Atrophy. J Neurol Neurol Disord 3(3): 303


Introduction
Temporal lobe epilepsy is the most common form of epilepsy with focal seizures in the adult population, approximately 60%.It is subdivided in mesial and neocortical or lateral.Underlying pathologies include tumors, vascular malformations, cortical dysplasia, trauma and hippocampal sclerosis [1].In literature, it is described that in mesial temporal lobe epilepsy with hippocampal sclerosis, during the crisis, occurs the presence of characteristic auras (upset malaise, fear, among others), followed by immobility, which is succeed by simple automatism, involuntary motor changes and consciousness compromise [1].Hyperkinetic crisis is uncommon, occurring in about 3% of the cases, with changes of facial expressions, vocalization, complex motor automatisms, dystonic posturing and cephalic version.Hyperkinetic crisis indicates strong association with the symptomatogenic frontal zone, mainly orbitofrontal or medial frontal [2].

Case Report
Patient F.R.S., male, 61 years old, who at the age of 21 presented a condition of dyscognitive seizures with vocal and complex automatisms like getting undressed and walking, besides tonic seizures, with the maximum duration of 2 minutes, daily frequency, about 5 episodes a day.He could not sense the phenomenon and denied postictal alteration, like somnolence or sphincteric release.In the previous pathological history reported only mild hypertension, but did not use any antihypertensive medication, denied trauma, previous surgeries, blood transfusions or fever seizures in childhood.He had previous drug treatment with valproic acid 1500mg/day, which did not change the number of episodes per day, so after a few months his doctor added carbamazepine 800mg/ day but, despite he did not have side effects and had good compliance with medication, there was no clinical improvement.So, he was sent to a Drug Resistant Epilepsy Center (DREC).By the time of the appointment at the DREC, he had been taking carbamazepine 800mg/day and phenobarbital 200mg/day, without improvement.He brought a head MRI that showed hippocampal asymmetry (Figure 1), so it was requested a video electroencephalogram.
By the time he was hospitalized, to do the video electroencephalogram, he had normal blood pressure, was mentally stable, his carbamazepine and phenobarbital levels were inside the therapeutic range.Analysis of the video electroencephalogram: seizure originates from parietal-occipital regions bilaterally with an alpha-like rhythmic activity followed in 2 seconds by hyperkinetic manifestation waked by vocalization, a body-turning to the right, a feared face, a tonic posturing of the left and lower upper limb.The EEG begins with a rhythmic alpha-like activity, in the posterior derivations P4-O2, P3-O1 bilaterally, spreads in 2 to 3 seconds to posterior temporal derivations.The EEG is them covered by artifacts.The seizure lasts about 63'' and ends with a return to the basal interictal activity.
As initial conduct we have chosen to reduce the use of phenobarbital and then place him on topiramate 100mg/day.It was put under increasing doses of topiramate up to 200mg/day and phenobarbital was waned off at a 25mg/day rate every 10 days.He progresses with sudden drops to the frequency of twice a week, besides the dyscognitive seizures.Patient's compliance was achieved and he turned out to be seizure-free in about 4 weeks.He is still been followed, in the Drug Resistant Epilepsy Center, monthly, and it has 4 months that he is seizure-free.
Currently, hypermotor seizure (HMS) is defined as bizarre, complex and high-amplitude movements, involving proximal segment and resulting in a violent and inappropriate movement.It occurs in 15 to 27% of frontal lobe epilepsies, particularly in the mesial area, or orbitofrontal, but it was also described in seizures originating in the dorsolateral region, in mesial region and neocortical of the temporal lobe, upper and anterior portions of the insular cortex and the parietal-temporal cortex (Figure 2A and 2B) [3,4].A mixed type of HMS1 and HMS2 was described in insular seizures, characterized mainly by repetitive pelvic, bimanual and bipedal movements, including pelvic thrusts and kicking.
HMS typically occurs at, or within 10 seconds after, the onset of the seizure.The average delay of HMS after the onset of the seizures helps distinguish the extrafrontal origin of HMS.The average delay between 4 and 30 seconds occurs in temporal epilepsy, 5 to 40 seconds in insular seizures and 10 to 35 seconds in posterior HMS [6].
Surgery in the posterior cortex is rarely performed, comparing to resections of the temporal and frontal lobes.The main reason is the difficulty in identifying the epileptogenic zone in the pre-operative assessment [6,7].
The International League against Epilepsy defined drug resistant epilepsy, as "a failure of equate trials of two tolerated, appropriately chosen and used anticonvulsant drug schedules (whether as monotherapies or in combination) to achieve sustained seizure freedom" [8].
First-generation or "old" AEDs such as carbamazepine, phenobarbital and phenytoin are enzyme inducers.Same examples of second-generation or "newer" AEDs are lamotrigine, gabapentin, topiramate.Carbamazepine, phenytoin, phenobarbital and primidone are broad-spectrum inducers because they stimulate the activity of many cytochrome P45 (CYP) enzymes as well as uridin-glucuronyl transferases (UGT) and epoxide hydrolase.
It is subdivided in 2 types: type HMS1, in which axial movements occur, that is movement around a vertical axis, while the semiology of type HMS2 occurs on a horizontal axis.HMS1 is associated to a epileptogenic zone in the ventromedial frontal cortex and HMS2 has been associated with a dorsal epileptogenic zone [4,5].The clinical differentiation consists of: type HMS1 has marked agitation and hypermotor behaviors with kicks, punches, swinging body and other motor signs, such as versive head movements, non-motor related signals, like facial expression of fear or anger, and dysautonomic symptoms.Subtype HMS2: a less intense agitation occurs with hypermotor behavior (trunk and pelvis rotation and other motor signals such as diatonic posture and versive movements of the head) [5].https://www.youtube.com/watch?v=Vkk0SUoK58cA report was made of a patient with hippocampal atrophy that presented type 2 hyperkinetic seizures (usually a frontal manifestation) with epileptogenic discharge in the parietal-occipital region.

Conclusion
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Figure 1 :
Figure 1: Magnetic resonance imaging, which shows hippocampal asymmetry that may correspond to left mesial temporal sclerosis Submit your manuscript at http://www.annexpublishers.com/paper-submission.php→ Easy online submission process → Rapid peer review process → Open access: articles available free online → Online article availability soon after acceptance for Publication → Better discount on subsequent article submission → More accessibility of the articles to the readers/researchers within the field