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复发性前庭性偏头痛眩晕发作与双侧严重前庭病的发生相关:病例系列

Recurrent Vestibular Migraine Vertigo Attacks Associated With the Development of Profound Bilateral Vestibulopathy: A Case Series.

作者信息

Wester Jacob L, Ishiyama Akira, Ishiyama Gail

机构信息

*Department of Head and Neck Surgery †Department of Neurology, University of California Los Angeles, Los Angeles, California.

出版信息

Otol Neurotol. 2017 Sep;38(8):1145-1148. doi: 10.1097/MAO.0000000000001486.

Abstract

BACKGROUND

Bilateral vestibulopathy (BVP) is a debilitating condition characterized by gait ataxia, oscillopsia, and imbalance.

OBJECTIVE

Case series of patients with migraine-linked vertigo spells and profound BVP. PATIENT 1:: A 69-year-old man presented with a history of recurrent severe vertigo spells lasting up to 3 days in duration associated with prostrating migraine headaches starting at age 60. His symptoms were misdiagnosed as an anxiety syndrome. At age 68, electronystagmography (ENG) revealed bilaterally absent caloric responses and complete BVP. His hearing was normal. PATIENT 2:: A 51-year-old man presented with a history of "earthquake-like" vertigo, sharp head pain, and phonophobia. These episodes occurred a handful of times over a 7-year period. Previous ENG testing at age 43 was normal. However, his ENG at age 48 revealed complete BVP. He was started on acetazolamide and noted improved balance, although subsequent ENG was unchanged. PATIENT 3:: A 49-year-old woman presented with a history of recurrent migraines with visual aura associated with vertigo lasting 1 hour. ENG at age 50 revealed complete BVP. Subjectively, she noted improved balance with acetazolamide and subsequent ENG demonstrated mild improvement. PATIENT 4:: A 43-year-old man presented with a 5-year history of optical migraines and recurrent vertigo spells, lasting 30 seconds, which was misdiagnosed as positional vertigo. He additionally had a 10-year history of oscillopsia. ENG at age 61 revealed complete BVP.

CONCLUSION

In these cases, vestibular migraine was linked to recurrent vertigo spells that eventually led to complete bilateral vestibulopathy.

摘要

背景

双侧前庭病变(BVP)是一种使人衰弱的病症,其特征为步态共济失调、视振荡和平衡失调。

目的

偏头痛相关性眩晕发作和严重双侧前庭病变患者的病例系列。

患者1:一名69岁男性,有复发性严重眩晕发作史,持续长达3天,伴有60岁起病的剧烈偏头痛性头痛。他的症状被误诊为焦虑综合征。68岁时,眼震电图(ENG)显示双侧冷热反应消失及完全性双侧前庭病变。他的听力正常。

患者2:一名51岁男性,有“地震样”眩晕、头部锐痛和畏声病史。这些发作在7年期间发生过几次。43岁时先前的眼震电图检查正常。然而,他48岁时的眼震电图显示完全性双侧前庭病变。他开始服用乙酰唑胺,平衡有所改善,尽管随后的眼震电图检查结果未变。

患者3:一名49岁女性,有复发性偏头痛伴视觉先兆,伴有持续1小时的眩晕病史。50岁时的眼震电图显示完全性双侧前庭病变。主观上,她注意到服用乙酰唑胺后平衡有所改善,随后的眼震电图显示有轻度改善。

患者4:一名43岁男性,有5年的视性偏头痛和复发性眩晕发作史,持续30秒,曾被误诊为位置性眩晕。他还有10年的视振荡病史。61岁时的眼震电图显示完全性双侧前庭病变。

结论

在这些病例中,前庭性偏头痛与复发性眩晕发作相关,最终导致完全性双侧前庭病变。

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