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1型晚发性发作性睡病中的猝倒状态伴快速眼动睡眠过多

Status Cataplecticus with Rapid Eye Movement Sleep Excess in Late-onset Narcolepsy Type 1.

作者信息

Ando Takashi, Wakai Masakazu, Kanbayashi Takashi, Katsuno Masahisa

机构信息

Department of Neurology, Nagoya University Graduate School of Medicine, Japan.

Department of Sleep Medicine, Chutoen General Medical Center, Japan.

出版信息

Intern Med. 2022 Oct 1;61(19):2951-2955. doi: 10.2169/internalmedicine.8465-21. Epub 2022 Mar 12.

DOI:10.2169/internalmedicine.8465-21
PMID:35283376
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9593136/
Abstract

A 57-year-old man presented with difficulty speaking and walking along with increased daytime somnolence. His symptoms fluctuated throughout the day but never completely disappeared. A neurological examination revealed mild dysarthria, limb weakness, and staggering gait. Polysomnography showed rapid eye movement (REM) sleep excess (55.0%). Multiple sleep latency tests revealed a mean sleep latency of zero minutes with sleep-onset REM periods in all naps. The Orexin-A concentration in the cerebrospinal fluid was low (50.8 pg/mL). Human leukocyte antigen testing demonstrated DQB1*0602 positivity. His neurological symptoms were relieved by clomipramine. Thus, he was diagnosed with late-onset narcolepsy type 1 with status cataplecticus.

摘要

一名57岁男性出现言语和行走困难,同时白天嗜睡加重。他的症状在一天中波动,但从未完全消失。神经系统检查发现轻度构音障碍、肢体无力和蹒跚步态。多导睡眠图显示快速眼动(REM)睡眠过多(55.0%)。多次睡眠潜伏期测试显示平均睡眠潜伏期为零分钟,所有小睡均出现睡眠起始REM期。脑脊液中食欲素-A浓度较低(50.8 pg/mL)。人类白细胞抗原检测显示DQB1*0602阳性。他的神经症状通过氯米帕明得到缓解。因此,他被诊断为伴有猝倒状态的晚发型1型发作性睡病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e758/9593136/52056383b0b7/1349-7235-61-2951-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e758/9593136/7d55f72011b9/1349-7235-61-2951-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e758/9593136/52056383b0b7/1349-7235-61-2951-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e758/9593136/7d55f72011b9/1349-7235-61-2951-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e758/9593136/52056383b0b7/1349-7235-61-2951-g002.jpg

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