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双侧前庭功能丧失。

Bilateral loss of vestibular function.

作者信息

Rinne T, Bronstein A M, Rudge P, Gresty M A, Luxon L M

机构信息

MRC Human Movement and Balance Unit, National Hospital for Neurology and Neurosurgery, London, United Kingdom.

出版信息

Acta Otolaryngol Suppl. 1995;520 Pt 2:247-50. doi: 10.3109/00016489509125239.

Abstract

The clinical findings in 53 patients with bilateral vestibular failure (BVF) seen in a neurological hospital are reported. Bilateral acoustic neuromas were excluded. Seven patients (13%) had progressive cerebellar degeneration; these patients had no hearing complaints but showed gait ataxia, abnormal eye movements and cerebellar atrophy on neuro-imaging. Referral in these patients was primarily for eye movement assessment, and BVF was usually unsuspected. Neuropathies were present in 5 patients (9%), usually with normal central (brainstem-cerebellar) ocular motor function and variable patterns of hearing loss. The single largest group was idiopathic BVF (11 patients, 21%), patients presenting with vertiginous episodes, progressive unsteadiness or brief paroxysms of oscillopsia; auditory function, eye movements, neurological examination and imaging were usually normal. Nine patients (17%) suffered ototoxicity, mostly due to gentamicin; hearing was normal or mildly impaired. In 6 patients (11%) BVF was post-meningitic, with concomitant auditory loss. Autoimmune disease was found in 5 patients (9%); other organs were involved by the disease, and hearing was impaired but eye movements were spared. Miscellaneous neurological, otological or neoplastic diseases accounted for the remaining 10 patients. This study suggests that i) in patients with cerebellar degenerations, BVF may be underdiagnosed as the unsteadiness may be attributed only to the cerebellar disorder, ii) some patients with idiopathic BVF present with only minor visual or vestibular symptoms, and iii) detailed immunological screenings should be undertaken more often, in view of the significant proportion of patients with autoimmune and idiopathic BVF.

摘要

本文报告了一家神经科医院收治的53例双侧前庭功能丧失(BVF)患者的临床症状。排除了双侧听神经瘤患者。7例(13%)患者出现进行性小脑变性;这些患者没有听力问题,但表现出步态共济失调、异常眼动,神经影像学检查显示小脑萎缩。这些患者主要因眼动评估前来就诊,通常未被怀疑患有BVF。5例(9%)患者存在神经病变,通常中枢(脑干 - 小脑)眼动功能正常,听力损失情况各异。最大的一组是特发性BVF(11例,21%),这些患者表现为眩晕发作、进行性步态不稳或短暂发作性视振荡;听觉功能、眼动、神经系统检查及影像学检查通常正常。9例(17%)患者发生耳毒性,主要由庆大霉素引起;听力正常或轻度受损。6例(11%)患者的BVF发生在脑膜炎后,伴有听力损失。5例(9%)患者患有自身免疫性疾病;疾病累及其他器官,听力受损但眼动功能未受影响。其余10例患者病因是其他各类神经、耳科或肿瘤性疾病。本研究表明,i)在小脑变性患者中,BVF可能未被充分诊断,因为步态不稳可能仅归因于小脑疾病,ii)一些特发性BVF患者仅表现出轻微的视觉或前庭症状,iii)鉴于自身免疫性和特发性BVF患者占相当比例,应更频繁地进行详细的免疫学筛查。

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