Compta Yaroslau, Iranzo Alex, Santamaría Joan, Casamitjana Roser, Graus Francesc
Neurology Service, Hospital Clinic, Institut D'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Sleep. 2007 Jun;30(6):767-9. doi: 10.1093/sleep/30.6.767.
A 69-year-old man with anti-Ma2 paraneoplastic encephalitis presented with subacute onset of severe hypersomnia, memory loss, parkinsonism, and gaze palsy. A brain magnetic resonance imaging study showed bilateral damage in the dorsolateral midbrain, amygdala, and paramedian thalami. Videopolysomnography disclosed rapid eye movement (REM) sleep behavior disorder, and a Multiple Sleep Latency Test showed a mean sleep latency of 7 minutes and 4 sleep-onset REM periods. The level of hypocretin-1 in the cerebrospinal fluid was low (49 pg/mL). This observation illustrates that REM sleep behavior disorder and narcoleptic features are 2 REM-sleep abnormalities that (1) may share the same autoimmune-mediated origin affecting the brainstem, limbic, and diencephalic structures and (2) may occur in the setting of the paraneoplastic anti-Ma2-associated encephalitis.
一名患有抗Ma2副肿瘤性脑炎的69岁男性,出现严重嗜睡、记忆丧失、帕金森综合征和凝视麻痹的亚急性发作。脑部磁共振成像研究显示双侧背外侧中脑、杏仁核和丘脑旁正中核受损。视频多导睡眠图显示快速眼动(REM)睡眠行为障碍,多次睡眠潜伏期测试显示平均睡眠潜伏期为7分钟,有4个睡眠起始REM期。脑脊液中食欲素-1水平较低(49 pg/mL)。这一观察结果表明,REM睡眠行为障碍和发作性睡病特征是两种REM睡眠异常,(1)可能具有相同的自身免疫介导起源,影响脑干、边缘系统和间脑结构;(2)可能发生在副肿瘤性抗Ma2相关脑炎的背景下。