DIAGNOSIS: KLEINE-LEVIN SYNDROME
The patient received a diagnosis of Kleine-Levin syndrome (sometimes spelled Klein Levin), a rare condition that can affect adolescents and young adults. It is more common in males than in females, but it can affect females as well. It is characterized by bouts of excessive sleepiness that last for weeks or months. His previous episode when he was 13 may have been a viral illness but could have been an earlier bout of this condition.
Young people with Kleine-Levin syndrome can have episodes characterized by sleeping for up to 20 hours per day. Fevers, muscle aches, and hyperphagia can accompany the episodes. Other behaviors that can occur during the episodes include moodiness, confusion, hallucinations, and uninhibited sexual behavior.1
Episodes of Kleine-Levin syndrome may last for several weeks or months. The condition resolves on its own without treatment. Episodes may recur several times throughout adolescence, and teenagers may have completely normal behavior and sleep patterns in between bouts of the illness. It is not associated with between-episode psychiatric problems, psychosis, behavioral problems, personality disorders, or drug use.
Kleine-Levin syndrome is a clinical diagnosis because there is no diagnostic test to identify or confirm the condition. It has been postulated to be triggered by a viral illness or hormonal dysfunction. Because of the symptoms, it may be mistaken for temporal lobe epilepsy, although electroencephalography can help distinguish the two conditions. The EEG tends to be normal. The polysomnogram shows decreased sleep efficiency with frequent waking from stage 2 sleep, normal sleep architecture, and an absence of shortened sleep latency or early REM sleep.2 These findings may occur with some other causes of adolescent and young adult hypersomnia, such as sleep deprivation or narcolepsy.
Standard imaging tests are normal, but functional MRI (fMRI) may show hypoperfusion and altered glucose metabolism in the tempoparietal and thalamic regions. Decreased connectivity between frontal eye fields and areas of the pons involved in REM sleep has been observed on fMRI, but the clinical significance of this finding is not clear.3
Lithium, valproic acid, and corticosteroids have been tried with some symptomatic improvement, but most patients do not respond to treatment.
Kleine-Levin syndrome has a reasonably good prognosis, with individual episodes spontaneously resolving, and a decrease in or complete discontinuation of further episodes during adulthood. Nevertheless, the illness has a substantial impact on quality of life, possibly affecting school work, social life, and participation in normal teenage activities. Support for families, including educating parents and the patient about potential complications such as hallucinations and emotional instability, can help in coping.
• A prolonged illness that seems like a viral infection should be evaluated
• Temporal lobe epilepsy should be considered when unexplained neuropsychological conditions arise
• Known abnormalities on brain fMRI may not be apparent on a standard brain MRI scan
1. Afolabi-Brown O, Mason TBA 2nd. Kleine-Levin syndrome. Paediatr Respir Rev. 2018;25:9-13. doi: 10.1016/j.prrv.2016.12.004.
2. Luo YW, Yu H, Yuan LH, Zhu GX. A polysomnography study of Kleine-Levin syndrome in a single center. Chin Med J (Engl). 2016;129:1565-1568. doi: 10.4103/0366-6999.184476.
3. Engström M, Latini F, Landtblom AM. Neuroimaging in the Kleine-Levin syndrome. Curr Neurol Neurosci Rep. 2018;18:58. doi: 10.1007/s11910-018-0866-y.