Gürkov R, Pyykö I, Zou J, Kentala E
Department of Otorhinolaryngology Head and Neck Surgery, University of Munich, Marchioninistr. 15, 81377, Munich, Germany.
German Centre for Vertigo and Balance Disorder, University of Munich, Marchioninistr. 15, 81377, Munich, Germany.
J Neurol. 2016 Apr;263 Suppl 1:S71-81. doi: 10.1007/s00415-015-7930-1. Epub 2016 Apr 15.
Menière's disease is a chronic condition with a prevalence of 200-500 per 100,000 and characterized by episodic attacks of vertigo, fluctuating hearing loss, tinnitus, aural pressure and a progressive loss of audiovestibular functions. Over 150 years ago, Prosper Menière was the first to recognize the inner ear as the site of lesion for this clinical syndrome. Over 75 years ago, endolymphatic hydrops was discovered as the pathologic correlate of Menière's disease. However, this pathologic finding could be ascertained only in post-mortem histologic studies. Due to this diagnostic dilemma and the variable manifestation of the various audiovestibular symptoms, diagnostic classification systems based on clinical findings have been repeatedly modified and have not been uniformly used in scientific publications on Menière's disease. Furthermore, the higher level measures of impact on quality of life such as vitality and social participation have been neglected hitherto. Recent developments of high-resolution MR imaging of the inner ear have now enabled us to visualize in vivo endolymphatic hydrops in patients with suspected Menière's disease. In this review, we summarize the existing knowledge from temporal bone histologic studies and from the emerging evidence on imaging-based evaluation of patients with suspected Menière's disease. These indicate that endolymphatic hydrops is responsible not only for the full-blown clinical triad of simultaneous attacks of auditory and vestibular dysfunction, but also for other clinical presentations such as "vestibular" and "cochlear Menière's disease". As a consequence, we propose a new terminology which is based on symptomatic and imaging characteristics of these clinical entities to clarify and simplify their diagnostic classification.
梅尼埃病是一种慢性病,每10万人中患病率为200 - 500例,其特征为发作性眩晕、波动性听力损失、耳鸣、耳内闷胀感以及听觉和前庭功能的进行性丧失。150多年前,普罗斯珀·梅尼埃首次认识到内耳是这种临床综合征的病变部位。75多年前,内淋巴积水被发现是梅尼埃病的病理相关因素。然而,这一病理发现只能在尸检组织学研究中确定。由于这种诊断困境以及各种听觉和前庭症状的表现各异,基于临床发现的诊断分类系统已被反复修改,且在关于梅尼埃病的科学出版物中未得到统一使用。此外,迄今为止,对生活质量影响较大的更高层次指标,如活力和社会参与度,一直被忽视。内耳高分辨率磁共振成像的最新进展现在使我们能够在体内观察疑似梅尼埃病患者的内淋巴积水情况。在本综述中,我们总结了颞骨组织学研究的现有知识以及基于影像学对疑似梅尼埃病患者评估的新证据。这些表明,内淋巴积水不仅是听觉和前庭功能同时发作的典型临床三联征的病因,也是其他临床表现,如“前庭性”和“耳蜗性梅尼埃病”的病因。因此,我们基于这些临床实体的症状和影像学特征提出了一种新的术语,以澄清和简化其诊断分类。