Yoshioka Daisuke, Yamanashi Takehiko, Iwata Masaaki
Division of Neuropsychiatry, Faculty of Medicine Tottori University Yonago Japan.
PCN Rep. 2025 Aug 29;4(3):e70199. doi: 10.1002/pcn5.70199. eCollection 2025 Sep.
Kleine-Levin syndrome (KLS) is a rare sleep disorder marked by recurrent episodes of severe hypersomnolence with accompanying cognitive, behavioral, or mood disturbances. Infections are frequently reported before symptom onset and have been proposed as potential triggers, although a definitive causal relationship has not been established. Although relapses of KLS after COVID-19 infection have been described, only one possible case of new-onset KLS associated with COVID-19 has been reported, in which a definitive diagnosis was not established.
We describe a 17-year-old male who developed KLS following a confirmed COVID-19 infection. After his clinical recovery, he began experiencing hypersomnolent episodes every few months, each lasting approximately 2 weeks and accompanied by decreased motivation and appetite. As the illness progressed, he developed persistent nausea lasting several weeks before each hypersomnolent episode, suggesting the emergence of a prodromal phase. Treatment with lithium and adjunctive modafinil showed limited efficacy in preventing recurrence or reducing episode severity. Each complete cycle comprising prodromal, hypersomnolent, and recovery phases lasted over a month and significantly disrupted his academic and social functioning.
This case represents the first diagnostically confirmed report of new-onset KLS following COVID-19 infection and suggests a possible autoimmune mechanism triggered by SARS-CoV-2. These findings emphasize the importance of comprehensive clinical assessment beyond objective test results and underscore the urgent need for effective treatment strategies tailored to the heterogeneous and disabling nature of KLS.
克莱恩-莱文综合征(KLS)是一种罕见的睡眠障碍,其特征为反复出现严重的嗜睡发作,并伴有认知、行为或情绪障碍。尽管尚未确定明确的因果关系,但在症状发作前经常有感染的报告,并被认为是潜在的触发因素。虽然已有关于COVID-19感染后KLS复发的描述,但仅报告了一例可能与COVID-19相关的新发KLS病例,且未确诊。
我们描述了一名17岁男性,在确诊COVID-19感染后患上了KLS。临床康复后,他开始每隔几个月就出现嗜睡发作,每次持续约2周,伴有动力和食欲下降。随着病情进展,他在每次嗜睡发作前出现持续数周的持续性恶心,提示前驱期的出现。锂盐和辅助使用莫达非尼治疗在预防复发或减轻发作严重程度方面疗效有限。每个完整周期包括前驱期、嗜睡期和恢复期,持续超过一个月,严重扰乱了他的学业和社交功能。
本病例是首例经诊断证实的COVID-19感染后新发KLS报告,提示可能存在由SARS-CoV-2触发的自身免疫机制。这些发现强调了超越客观测试结果进行全面临床评估的重要性,并突出了迫切需要针对KLS的异质性和致残性制定有效的治疗策略。