伴有小纤维神经病变和复发性晕厥的超活动型ehers - danlos综合征脱位风暴所致的失眠。

IF 1.8 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
European Journal of Translational Myology Pub Date : 2025-06-27 Epub Date: 2025-04-16 DOI:10.4081/ejtm.2025.12946
Josef Finsterer
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引用次数: 0

摘要

目的:报道1例伴有SFN的多动性埃勒-丹洛斯综合征(EDS)患者睡眠时频繁脱位导致睡眠剥夺。病例报告:患者是一名19岁的女性,患有过度活动的EDS,表现为频繁的大关节脱位和小纤维神经病变(SFN),表现为复发性晕厥。这种脱位是自发发生的,或者是由频繁的自愿或非自愿的运动引起的,即使在夜间,睡眠也会受到干扰。最长睡眠时间在4到5个小时之间。床上用品、止痛剂、肌肉松弛剂和物理疗法只能略微改善脱位引起的疼痛和不适。结论:本病例表明,过度移动的EDS可表现为失眠,这是由于夜间频繁脱位引起的疼痛和不适。活动性EDS患者应进行多导睡眠图检查,以确定睡眠障碍的原因,及时对失眠进行最合适的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Insomnia due to a dislocation storm in hypermobile Ehlers-Danlos syndrome with small fibre neuropathy and recurrent syncope.

Objective: To report on a patient with hypermobile Ehlers-Danlos syndrome (EDS) with SFN in whom frequent dislocations during sleep led to sleep deprivation.

Case report: The patient is a 19-year-old female with hypermobile EDS manifested by frequent dislocations of large joints and small fiber neuropathy (SFN) presenting as recurrent syncope. The dislocations occurred spontaneously or triggered by voluntary or involuntary movements with such frequency, even during the night, that sleep was disturbed. The maximum sleep duration was between 4 and 5 hours. Bedding, analgesics, muscle relaxants and physiotherapy only marginally improved the pain and discomfort caused by the dislocations.

Conclusions: This case demonstrates that hypermobile EDS can manifest phenotypically with insomnia due to pain and discomfort from frequent dislocations during the night. Patients with hypermobile EDS should undergo polysomnography to determine the cause of the sleep disturbance and initiate the most appropriate treatment for insomnia in a timely manner.

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来源期刊
European Journal of Translational Myology
European Journal of Translational Myology MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.30
自引率
27.30%
发文量
74
审稿时长
10 weeks
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