From ancient times the term vertigo and epilepsy have been linked conceptually and diagnostically. Bladin’s excellent historical review of “epileptic vertigo” documents that in second century A.D. Arataeus stated that if vertigo proved incurable, it might be the beginning of chronic epilepsy (Bladin, 1998) whilst vertigo was also reported to be considered “a little epilepsy” (Temkin, 1994).

However, the term vertigo had a much looser definition than the illusion of surrounding or self-motion understood in present times and was considered more a manifestation of a non-specific paroxysmal cerebral disturbance (Gizzy and Diamond, 2005). It was only when analysis of the sense of motion began in the late 19th century (Baloh, 2001) did the modern understanding of vertigo as a predominantly otogenic symptom arising from the vestibular system take hold.

Vertigo and epilepsy was first formally linked and consolidated into the term “epileptic vertigo” during the pioneering years of the scientific study of epilepsy in 18th and 19th century by French clinicians. Esquirol in 1838 first introduced the concept as a grade of epileptic severity that included “vertige epileptique,” “petit mal” and “grand mal” (cited in Temkin, 1994) and even with the introduction of absences to describe minor epileptic episodes, the term persisted.

Generalized seizures were considered to originate from the upper brainstem, but the condition of epileptic vertigo was thought to be localized to the hemispheres and to play a role in the mental symptoms of epilepsy. This poorly defined clinical entity developed negative connotations after research from the asylums of Paris associated aberrant behavioral episodes of the patients with brief incomplete epileptic attacks. Epileptic vertigo and thus epilepsy soon became popularly linked with the potential to suffer acute attacks of wayward potentially violent behavior (review in Bladin, 1998). The term remained in general use until the early 20th century and was accepted by many of the prolific authors of the time (Gizzy and Diamond, 2005), including Hughling Jackson:

“I believe that epileptic vertigo, epileptic petit-mal, and epileptic grand-mal are when regarded from an anatomical and physiological point of view simply differing degrees, that is to say they depend on different strengths of discharge...” (Hughlings Jackson, 1931).

However, the definition of the condition continued to lack of clarity leading to considerable disagreement (Bladin, 1998).

In 1861 Meniere’s localisation of vertigo to the inner ear drove the conceptual separation of vertigo from epilepsy (Baloh, 2001), though the shift did not occur immediately.

By the 1870’s Charcot, Jackson and Gowers had recanted their early concepts and strongly accepted that most vertigo emanated from the inner ear (Gordon, 1999).

In the Borderlands of Epilepsy 1907 (Gowers, 1907), Gowers remarks on the former imprecise descriptions of vertigo: “The sense in which it is popularly used is very wide and includes every peculiar vague brain sensation, especially brief obscuration of consciousness, imperfect perception of surroundings and the like.”

By the end of the 19th century, most authors had assigned vertigo to conditions other than epilepsy. If associated with epilepsy, vertigo was considered a symptom that may be felt at the onset of a seizure and even if it accompanied epilepsy, it conferred nothing of significance regarding classification or degree of severity (Bladin, 1998).

However, Gowers, being a master of medical observers, was probably the only great author in the late 19th century to still be able to consider it as a possible epileptic symptom and made great effort in making the distinction between the two entities.

“The attacks of minor epilepsy which are characterized by vertigo have to be distinguished from the other form of sudden giddiness” (Gowers, 1906).

The term epileptic vertigo did not disappear from the literature. It continues along with epileptic dizziness, epileptic nystagmus and epileptic tinnitus as conditions purely describing the predominant symptom associated with a seizure or epilepsy (Esquirol cited in Temkin, 1994).

As the field of epileptology advanced with the widespread acceptance of a cortical basis to seizure genesis, the 20th century saw more directed effort to understand the cortical substrate for the production of vertigo and vestibular disturbance associated with focal epileptic activity.

The electrical stimulation studies in humans and monkeys in the early part of the century gave the first insight to anatomical basis of the vestibular cortex whereas more recently advances have been made by the combination of intracranial stimulation studies in medically intractable epilepsy patients and modern electroencephalography (EEG) techniques, structural and functional imaging (reviewed in Lopez and Blanke, 2011).

During electrical cortical stimulation in awake patients undergoing brain surgery Foerster demonstrated that stimulation of the intraparietal sulcus elicited full body rotations in space (Foerster, 1936), whereas a few years later stimulation of the superior temporal gyrus in patients operated on for focal epilepsy was associated with the sensations of “swinging, spinning,” “sinking feeling” and “head jumping up and down” (Penfield and Kristiansen, 1951; Penfield and Jasper, 1954; Penfield, 1957)

More recently a new insight has been gained from a retrospective systematic study of intracranial electrical stimulation using depth electrodes in 44 refractory epilepsy patients (Kahane et al., 2003). It reported a wide distribution of anatomical sites from which vestibular sensations were electrically induced though confirmed that most sites were in the temporal and parietal areas. The authors suggested the presence of a human temporo-peri-Sylvian vestibular cortex (TPSVC), a possible equivalent to the monkey’s polysensory PIVC, but involving the insula less as stimulation of the insula infrequently evoked conscious vestibular sensations (Isnard et al., 2004). Stimulation of the parietal lobe more posteriorly, in area 39 near the angular gyrus has elicited non-specific vestibular sensations (Blanke et al., 2002). The angular gyrus has been previously proposed as the “epicenter of the vestibulo-psychic area” on the basis of lesional studies in epileptic patients (Smith, 1960). The data obtained from human stimulation studies are summarized in Figure 1.

The authors of the large retrospective intracerebral stimulation study were able to propose anatomical correlates to certain types of vestibular sensations (Kahane et al., 2003). Pitch plane illusions were mainly elicited from the parietal operculum and yaw plane illusions from the temporal cortex. Translational linear illusions were more frequently elicited by stimulation of the mesial structures, in particular the mesial parietal cortex. In a separate case report, stimulation of the right paramedian precuneus also reproduced the epileptic linear self-motion perception (Wiest et al., 2004). Another study using subdural grids, induced rotational and swaying bidirectional vestibular sensations by stimulating two adjacent sites at the anterior part of the intraparietal sulcus (Blanke et al., 2000).

This could suggest a three-dimensional coding of spatial information according to anatomical site, and the increasing complexity of bidirectional vestibular sensations could reflect higher level processing such as shown with the progressive increase in complexity the hierarchical organization of the visual and auditory systems.

Although this data contributes considerably to the understanding of the vestibular system a caveat to the stimulation on epileptic cortices is the possibility of cortical plasticity associated with recurrent seizures. This could explain the inter-individual variability in the studies.

As well as the cortical stimulation studies, data has been gained by the close study of the electroclinical characteristics of focal seizures associated with vestibular dysfunction. Early studies in the 20th century (Penfield and Kristiansen, 1951; Smith, 1960) localized focal epileptic discharges associated with vertigo to the superior temporal gyrus and the temporo-parietal cortex.

A particularly detailed clinical study of 120 patients revealed the commonest symptoms were the sense of rotational vertigo predominantly in the yaw and roll planes, linear translational illusions or a combination (Smith, 1960). More complex vestibular dysfunctions such as the sensation of floating, the anticipation of spinning and unsteadiness were also described supporting the theory of higher levels of organization (Figure 2).

More recently focal seizure activity associated with vestibular illusions of rotation involving of the temporo-parieto-occipital (TPO) junction has been demonstrated by stereotactic EEG (SEEG) recordings (Barba et al., 2007) and in a case using interictal SPECT and scalp EEG (Jaffe et al., 2006). Parietal seizures have been known to be often associated with vestibular sensations (Salanova et al., 1995), but in a recent SEEG study of the epileptogenic networks underlying parietal lobe seizures, vestibular sensations were associated with seizures arising from the superior parietal region (Bartolomei et al., 2011), in keeping with stimulation studies of intraparietal sulcus eliciting vestibular responses (Blanke et al., 2000). Parietal seizures could also elicit vestibular symptoms by interfering with areas associated with representation of the body in space (Blanke et al., 2000).

Vestibular symptoms are occasionally reported in other localisations, particularly in frontal lobe seizures (Lopez et al., 2010).

Focal seizures associated with vestibular sensations arising from these multiple distinct cortical areas is in keeping with current theories of a widespread vestibular multisensory cortical network (Lopez and Blanke, 2011).

Vestibular epilepsy is characterized by focal seizures with vestibular symptoms as either the sole or predominant feature. The vestibular symptoms can range from mild disequilibrium to frank vertigo in any plane of action (yaw, pitch, roll, linear), however, it is rare however to have purely vestibular symptoms. The most common accompanying symptoms are nausea or vomiting and tinnitus (Brandt, 2003; Hewett et al., 2011) but other well documented symptoms including ipsilateral and contralateral parasthesias, olfactory and gustatory hallucinations, depersonalisation, epigastric discomfort, anxiety and deja-vu which almost certainly reflect local seizure propagation (Kogeorgos et al., 1981).

Body or head and eye rotation with or without nystagmus is considered to be frequent in some descriptions, however this is not noted in the two published case series (Kogeorgos et al., 1981; Hewett et al., 2011).

A short period of altered consciousness has been considered a central characteristic of the epilepsy (Alpers, 1960). 50% of patients in series described by Kogeorgos et al. (1981) had brief “absences” with 23% having generalized tonic-clonic seizures (GTCS). 65% of patients had full loss of consciousness with a fall in the recent case series, though only 21% had GTCS (Hewett et al., 2011). In this series, a cardiogenic syncope (two had paroxysmal atrial fibrillation, and one with transient asystole during a focal seizure) or a vasovagal syncope (positive tilt table test) may have accounted for some of the loss of consciousness and fall. This association may just suggest epilepsy with concurrent cardiovascular disease, but in this young age group, it may suggest a link between the two conditions, particularly a predisposition for vasovagal hyperactivity.

The duration of seizures can be variable but is usually brief lasting a few seconds, though there are some patients reporting seizures lasting many minutes (Hewett et al., 2011). The symptoms are typically paroxysmal beginning suddenly and unless the seizure secondarily generalizes they usually discontinue abruptly. In cases of pure vestibular symptomatology these features can be particularly helpful in differentiating from other vertiginous diagnoses (see below; Alpers, 1960; Brandt, 2003).

A diagnosis will be heavily supported by positive EEG findings and lateral temporal epileptic foci are frequent (Alpers, 1960; Brandt, 2003).

In the series described by Kogeorgos et al. (1981) an abnormal interictal EEG was a major criterion for the diagnosis. 28/30 had a temporal or bitemporal abnormalities, in some associated with generalized seizure discharges. There was a left temporal emphasis in 50%, right in 25% and bitemporal in 20%. The other two had atypical generalized patterns.

In the series described by Hewett et al. (2011), the predominant features on interictal scalp EEG were abnormalities over the parietal or TPO areas (Figure 3). Many of these activities are close in their morphology and topography to lambda waves and are therefore difficult to distinguish from physiological activity. A right side predominance was also found in this series.

A family history of epilepsy was elicited in 20% (Kogeorgos et al., 1981) and 29% (Hewett et al., 2011) had some form of family history but none with first-degree relative. A genetic link is therefore possible in these cases and a family history of epilepsy is a helpful feature in differentiating from the other vestibular syndromes.

Vestibular seizures are considered to respond well to anti-epileptic medication (Brandt, 2003). In the oldest series, over half of the patients had complete remission with phenytoin or carbamazepine with a considerable reduction in the frequency and severity of attacks with the remainder who complied (Kogeorgos et al., 1981). All the patients that complied to treatment (12/14) in the other case series were seizure free at time of publication on either mono or dual therapy with more modern medication (Hewett et al., 2011).