Clinical review

Narcolepsy mistaken for epilepsy

Adam Zeman, consultant neurologist ^a, Neil Douglas, professor ^b, Rebecca Aylward, locum consultant neurologist ^c. 

^a Department of Clinical Neurosciences, Western General Hospital, Edinburgh EH2 2XU, ^b Sleep Laboratory, Royal Infirmary of Edinburgh, Edinburgh EH3 9YW, ^c Epilepsy Clinic, Falkirk Royal Infirmary, Falkirk FK1 5QE

Correspondence to: A Zeman az{at}skull.dcn.ed.ac.uk

Narcolepsy is a distinctive but underdiagnosed disorder of sleep and waking. Its cardinal manifestations are: (a) excessive daytime sleepiness, with a tendency to nap repeatedly through the day; (b) cataplexy, a loss of muscle tone triggered by emotion, causing immobility for seconds to minutes; (c) hypnagogic hallucinations, vivid visual or auditory phenomena, experienced at the onset of sleep; and (d) sleep paralysis, an inability to move on first awakening.¹

When a patient describes all these symptoms the diagnosis should be straightforward. Diagnostic difficulty arises when patients present with isolated symptoms, or if their story suggests some more familiar diagnosis. We report on three patients recently encountered in whom narcolepsy was initially mistaken for epilepsy. Indeed, Gelineau, the French physician who coined the term "narcolepsy" in 1880, was at pains to distinguish his novel disorder of sleep (narco from the Greek for "sleep" and "lepsy" for taken hold by) from epilepsy, with which he thought it might be confused. ^{2 3}

	Case reports

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Case 1A 26 year old woman was found in the bath "unable to move, speak, or get out." Her husband reported flickering of the eyelids and muscle twitching. Her speech was slurred as she recovered, over minutes. The referral letter noted a history of short periods of apparent daytime sleep, sometimes at inappropriate momentsfor example, during mealsand a tendency to "go weak and limp . . . if she is having a carry-on or laughing heartily." The diagnosis at referral was of complex partial seizures; sodium valproate had been prescribed. It emerged that she had clear recall of her period of immobility in the bath: it resembled her episodes of weakness on laughing. On direct questioning she described sleep paralysis and hypnagogic hallucinations. She tended to sleep poorly at night. The combination of daytime sleepiness, cataplexy, sleep paralysis, and hypnagogic hallucinations suggested narcolepsy. Her HLA type, determined by the microlymphocytotoxicity technique using commercially obtained antisera, was DR15², DQ6¹, consistent with narcolepsy. Overnight polysomnography gave normal results, but a multiple sleep latency test gave a mean sleep onset time of 4 minutes (normally more than 10), with rapid eye movement sleep in the first 15 minutes of two of her five recorded naps (normally none). These results confirmed the diagnosis. Sodium valproate was withdrawn. Clomipramine controlled her cataplexy; her daytime sleepiness has improved on treatment with stimulants.

Case 2A 23 year old builder complained of excessive sleepiness over two years causing difficulties at work. His general practitioner was concerned by the possibility of epilepsy. Assessment in a general medical clinic elicited a story of "tonic-clonic seizures which occur during sleep," based on a description from his girlfriend. He was a loud snorer. An electroencephalogram gave a normal recording, but he became drowsy repeatedly during the procedure. We subsequently obtained a history of disabling episodes of cataplexy: he had learnt to keep a straight face to avoid laughter and the resulting weakness. He also reported sleep paralysis and hypnagogic hallucinations. The true nature of the tonic-clonic seizures during sleep eventually became clear: these were episodes of cataplexy with distal muscle twitching, occurring towards the climax of sexual intercourse. His HLA type, determined by the microlymphocytotoxicity technique, was DR15², Drw53, DQ1,3, consistent with narcolepsy. Overnight polysomnography suggested mild obstructive sleep apnoea, but a multiple sleep latency test was indicative of narcolepsy, with a mean sleep latency of 15 seconds and sleep onset rapid eye movement in all four naps. Fluoxetine has controlled his cataplexy; stimulants for his daytime sleepiness and continuous positive airways pressure at night for his sleep apnoea have made a modest impact.

Case 3A 41 year old retired social worker was referred from an epilepsy clinic. Fifteen years before she had begun to experience episodes resembling "a waking dream:" something familiar would come into her mind, but she would be unable to recall its content afterwards. Six years before these episodes had become more sustained. She developed the sense that there "was a film running in my head," comprising intrusive mental contents, both images and thoughts. She also experienced occasional feelings of déjà vu. Temporal lobe epilepsy was suspected. Computed tomography of the brain and an electroencephalogram gave normal results; treatment with carbamazepine was ineffective. Two years before we saw her the "film running in the head" had resolved itself into individual pictures that entered her mind for a second or so at a time. She sometimes recognised these from recent dreams, and they tended to have a strong emotional content. They appeared three or four times a day; she had similar experiences on dropping off to sleep, when she felt that "a dream comes straight into my mind." Seven episodes of "waking hallucination" occurred during a 24 hour electroencephalogram recording: during several of these the record showed light sleep with superimposed rapid eye movements. Rapid eye movement also occurred at the onset of overnight sleep. On direct questioning she admitted to daytime sleepiness, with naps at least once a day, but not to cataplexy or sleep paralysis. We believed that her "waking hallucinations" represented a variety of hypnagogic hallucinations, and that these, in combination with daytime sleepiness and sleep onset rapid eye movement, were suggestive of narcolepsy (perhaps not conclusive, however, as some authors require the presence of cataplexy for a definite diagnosis⁴). Her HLA type, determined by polymerase chain reaction amplification with sequence specific primers, was DRB1*15, DRB5*51, DQB1*6, consistent with narcolepsy. A multiple sleep latency test showed a mean sleep latency of 11 minutes, a minimum latency of seven minutes, and two episodes of sleep onset rapid eye movement.

	Discussion

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Narcolepsy has a prevalence of around 1:2000. ^{5 6} It can present at any age, most often in the second and third decades of life.⁴ A history of excessive daytime sleepiness and cataplexy make the diagnosis extremely likely, but the disorder can present with any combination of excessive daytime sleepiness, cataplexy, hypnagogic hallucinations, and sleep paralysis. HLA typing reveals the DQB1 0602 subtype in 90% of people with narcoplepsy compared with 12-38% of controls, but the possession of this allele is neither necessary nor sufficient for the disorder.⁷ Overnight polysomnography (box) helps to rule out other causes of excessive sleep disorder, such as obstructive sleep apnoea. The multiple sleep latency test (box) generally shows a reduced mean sleep latency and, usually, the occurrence of episodes of sleep onset rapid eye movement.⁴

The phenomenon of narcolepsy can be understood in terms of a dysregulation of rapid eye movement sleep, which is normally associated with dreaming and motor inhibition to prevent the dreams from being acted out.⁸ The inappropriate activation of these mechanisms underlies hypnagogic hallucinations, cataplexy, and sleep paralysis. Effective treatment is available.⁴ Tricyclic antidepressants and selective serotonin reuptake inhibitors reduce the frequency of attacks of cataplexy, and stimulants including dexamphetamine, methylphenidate, and modafinil reduce the frequency and intensity of sleep attacks.

In cases 1 and 2, diagnostic difficulty stemmed from the misinterpretation of episodes of cataplexy and daytime sleep. Partial recovery of muscle tone, with resulting twitching movements, is common during episodes of cataplexy⁴: this was mistaken for the jerking of a seizure in both cases. Clues to the true nature of these episodes were supplied by both patients having all the symptoms of narcolepsy, their recall for events occurring during their attacks of weakness, and the precipitation of the nocturnal attacks by sexual excitement in case 2. In case 3, the description of elusive reminiscences and déjà vu gave rise to a reasonable suspicion of temporal lobe seizures. However, the patient's own impression that these experiences represented "waking dreams" was born out by investigation.

These cases illustrate the scope for mistaking narcolepsy for epilepsy. The investigation, management, and prognosis of these two conditions are so different that this error should be avoided. Considering the possibility of narcolepsy and inquiring about its four principal symptoms will usually achieve this goal.

	Acknowledgments

We thank Dr Roger Cull for discussion of the electroencephalograms and Dr Audrey Todd for advice on the HLA typing.

Contributors: AZ assessed cases 1 and 2 and came up with the idea for the paper; he will act as guarantor for the paper. ND assessed all three patients in the Sleep Laboratory. RA established the diagnosis in case 3. The paper was written jointly by the three authors.

	Footnotes

Competing interests: AZ and ND received travel expenses and a speaker's fee from Cephalon.

	References

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(Accepted 3 October 2000)