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前庭神经鞘瘤患者的前庭功能与生活质量:肿瘤大小是否重要?

Vestibular function and quality of life in vestibular schwannoma: does size matter?

机构信息

Department of Neurology, Ludwig-Maximilians University Munich, Germany.

出版信息

Front Neurol. 2011 Aug 30;2:55. doi: 10.3389/fneur.2011.00055. eCollection 2011.

Abstract

OBJECTIVES

Patients with vestibular schwannoma (VS) frequently suffer from disabling vestibular symptoms. This prospective follow-up study evaluates vestibular and auditory function and impairment of quality of life due to vertigo, dizziness, and imbalance in patients with unilateral VS of different sizes before/after microsurgical or radiosurgical treatment.

METHODS

Thirty-eight patients with unilateral VS were included. Twenty-two received microsurgery, 16 CyberKnife radiosurgery. Two follow-ups took place after a median of 50 and 186.5 days. Patients received a standardized neuro-ophthalmological examination, electronystagmography with bithermal caloric testing, and pure-tone audiometry. Quality of life was evaluated with the Dizziness Handicap Inventory (DHI). Patient data was grouped and analyzed according to the size of the VS (group 1: <20 mm vs group 2: ≥20 mm).

RESULTS

In group 1, the median loss of vestibular function was +10.5% as calculated by Jongkees Formula (range -43 to +52; group 2: median +36%, range -56 to +90). The median change of DHI scores was -9 in group 1 (range -68 to 30) and +2 in group 2 (-54;+20). Median loss of hearing was 4 dB (-42; 93) in group 1 and 12 dB in group 2 (5; 42).

CONCLUSION

Loss of vestibular function in VS clearly correlates with tumor size. However, loss of vestibular function was not strictly associated with a long-term deterioration of quality of life. This may be due to central compensation of vestibular deficits in long-standing large tumors. Loss of hearing before treatment was significantly influenced by the age of the patient but not by tumor size. At follow-up 1 and 2, hearing was significantly influenced by the size of the VS and the manner of treatment.

摘要

目的

前庭神经鞘瘤(VS)患者常遭受致残性前庭症状。本前瞻性随访研究评估了单侧 VS 大小不同的患者在显微手术或放射外科治疗前后的前庭和听觉功能以及因眩晕、头晕和失衡导致的生活质量受损。

方法

共纳入 38 例单侧 VS 患者。22 例接受了显微手术,16 例接受了 CyberKnife 放射外科手术。两次随访分别在中位随访时间为 50 和 186.5 天后进行。患者接受了标准化的神经眼科检查、双耳冷热试验和纯音测听。使用眩晕障碍量表(DHI)评估生活质量。根据 VS 的大小将患者数据分组并进行分析(组 1:<20mm 与组 2:≥20mm)。

结果

在组 1 中,根据 Jongkees 公式计算,前庭功能丧失的中位数为+10.5%(范围-43 至+52;组 2:中位数+36%,范围-56 至+90)。DHI 评分中位数变化在组 1 中为-9(范围-68 至 30),在组 2 中为+2(范围-54 至+20)。组 1 听力损失中位数为 4dB(范围-42 至 93),组 2 听力损失中位数为 12dB(范围 5 至 42)。

结论

VS 中的前庭功能丧失与肿瘤大小明显相关。然而,前庭功能丧失与长期生活质量恶化并无严格关联。这可能是由于长期大肿瘤导致的前庭功能缺陷的中枢代偿。治疗前听力损失明显受患者年龄影响,但不受肿瘤大小影响。在随访 1 和 2 时,听力明显受 VS 大小和治疗方式的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a6f/3171060/fbe72427f8ea/fneur-02-00055-g001.jpg

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