Corticosteroid-responsive narcolepsy type II after COVID-19: A relevant differential diagnosis of post-COVID syndrome (a case report).

IF 3.4 3区 医学 Q2 CLINICAL NEUROLOGY Journal of Sleep Research Pub Date : 2024-12-02 DOI:10.1111/jsr.14406
Erika C S Künstler, Solveig Menrad, Isabelle Utech, Kathrin Finke, Sven Rupprecht
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Abstract

Excessive daytime sleepiness is a possible symptom of post-COVID syndrome and is also the cardinal symptom of narcolepsy, a rare life-long sleep disorder with a possible autoimmune background. Recent reports indicate that COVID-19 infection may trigger narcolepsy. However, it remains unclear how best to identify and treat such cases. A 25-year-old male developed daytime sleepiness after COVID-19 infection. A diagnosis of narcolepsy type II was made based on pathologically shortened sleep latencies in polysomnography and multiple sleep latency tests (MSLT) together with several sleep-onset REM-sleep periods (SOREMs). Pupillography and neuropsychological testing revealed reduced alertness levels. Hypocretin levels in the cerebrospinal fluid were borderline. Based on the postulated autoimmune background of narcolepsy, we performed an intravenous high-dose corticosteroid pulse therapy with methylprednisolone. Narcoleptic symptoms immediately and consistently remitted after the corticosteroid pulse. Follow-up after 4 months revealed normalisation of sleep latencies, no further SOREMs in the MSLT, and increased alertness in pupillography and neurocognitive testing. No further wakefulness promoting drug therapy was required. Narcolepsy should be considered in the differential diagnosis of post-COVID syndrome with leading symptoms of daytime sleepiness. Furthermore, immunosuppressive therapy may offer a treatment option in managing an otherwise lifelong disorder in select cases.

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COVID-19后II型糖皮质激素反应性发作性睡病:COVID-19后综合征的相关鉴别诊断(1例报告)
白天过度嗜睡是covid后综合征的可能症状,也是发作性睡病的主要症状,发作性睡病是一种罕见的终身睡眠障碍,可能有自身免疫性背景。最近的报告表明,COVID-19感染可能引发嗜睡症。然而,目前尚不清楚如何最好地识别和治疗此类病例。一名25岁的男性在感染COVID-19后出现白天嗜睡。根据多导睡眠图和多次睡眠潜伏期试验(MSLT)的病理性睡眠潜伏期缩短以及几个睡眠发作的快速眼动睡眠期(SOREMs),诊断为II型发作性睡病。瞳孔地理学和神经心理学测试显示警觉性水平降低。脑脊液下丘脑泌素水平处于临界状态。基于假定的发作性睡病自身免疫性背景,我们进行了甲泼尼龙静脉注射大剂量皮质类固醇脉冲治疗。发作性睡症症状在皮质类固醇脉冲治疗后立即持续缓解。4个月后的随访显示睡眠潜伏期正常化,MSLT中没有进一步的sorem,并且瞳孔定位和神经认知测试的警觉性增加。不需要进一步的清醒促进药物治疗。以白天嗜睡为主要症状的新冠肺炎后综合征的鉴别诊断应考虑发作性睡。此外,免疫抑制疗法可能在某些情况下提供一种治疗选择,以管理其他终身疾病。
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来源期刊
Journal of Sleep Research
Journal of Sleep Research 医学-临床神经学
CiteScore
9.00
自引率
6.80%
发文量
234
审稿时长
6-12 weeks
期刊介绍: The Journal of Sleep Research is dedicated to basic and clinical sleep research. The Journal publishes original research papers and invited reviews in all areas of sleep research (including biological rhythms). The Journal aims to promote the exchange of ideas between basic and clinical sleep researchers coming from a wide range of backgrounds and disciplines. The Journal will achieve this by publishing papers which use multidisciplinary and novel approaches to answer important questions about sleep, as well as its disorders and the treatment thereof.
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