Strupp Michael, Lopez-Escamez Jose A, Kim Ji-Soo, Straumann Dominik, Jen Joanna C, Carey John, Bisdorff Alexandre, Brandt Thomas
Department of Neurology and German Center for Vertigo and Balance Disorders, University Hospital Munich, University of Munich, Germany.
Otology and Neurotology Group CTS495, Department of Genomic Medicine - Centre for Genomics and Oncology Research - Pfizer/Universidad de Granada/Junta de Andalucía (GENyO), PTS, Granada and Department of Otolaryngology, University Hospital Granada, Spain.
J Vestib Res. 2016;26(5-6):409-415. doi: 10.3233/VES-160589.
This paper describes the diagnostic criteria for vestibular paroxysmia (VP) as defined by the Classification Committee of the Bárány Society. The diagnosis of VP is mainly based on the patient history and requires: A) at least ten attacks of spontaneous spinning or non-spinning vertigo; B) duration less than 1 minute; C) stereotyped phenomenology in a particular patient; D) response to a treatment with carbamazepine/oxcarbazepine; and F) not better accounted for by another diagnosis. Probable VP is defined as follows: A) at least five attacks of spinning or non-spinning vertigo; B) duration less than 5 minutes; C) spontaneous occurrence or provoked by certain head-movements; D) stereotyped phenomenology in a particular patient; E) not better accounted for by another diagnosis.Ephaptic discharges in the proximal part of the 8th cranial nerve, which is covered by oligodendrocytes, are the assumed mechanism. Important differential diagnoses are Menière's disease, vestibular migraine, benign paroxysmal positional vertigo, epileptic vestibular aura, paroxysmal brainstem attacks (in multiple sclerosis or after brainstem stroke), superior canal dehiscence syndrome, perilymph fistula, transient ischemic attacks and panic attacks. Current areas of uncertainty in the diagnosis of VP are: a) MRI findings of vascular compression which are not diagnostic of the disease or predictive for the affected side because they are also observed in about 30% of healthy asymptomatic subjects; and b) response to treatment with carbamazepine/oxcarbazepine supports the diagnosis but there are so far no randomized controlled trials for treatment of VP.
本文描述了由巴兰尼协会分类委员会定义的前庭阵发性眩晕(VP)的诊断标准。VP的诊断主要基于患者病史,且需要满足:A)至少十次自发性旋转或非旋转性眩晕发作;B)持续时间少于1分钟;C)特定患者的刻板现象学表现;D)对卡马西平/奥卡西平治疗有反应;以及F)不能用其他诊断更好地解释。疑似VP的定义如下:A)至少五次旋转或非旋转性眩晕发作;B)持续时间少于5分钟;C)自发出现或由特定头部运动诱发;D)特定患者的刻板现象学表现;E)不能用其他诊断更好地解释。推测其机制是第8颅神经近端的触突性放电,该部位由少突胶质细胞覆盖。重要的鉴别诊断包括梅尼埃病、前庭性偏头痛、良性阵发性位置性眩晕、癫痫性前庭先兆、阵发性脑干发作(在多发性硬化症或脑干中风后)、上半规管裂综合征、外淋巴瘘、短暂性脑缺血发作和惊恐发作。目前VP诊断中存在不确定性的方面有:a)血管压迫的MRI表现不能诊断该病或预测患侧,因为在约30%的健康无症状受试者中也可观察到;b)对卡马西平/奥卡西平治疗的反应支持诊断,但迄今为止尚无治疗VP的随机对照试验。