Cochleovestibular nerve involvement in sarcoidosis: a case series and a literature review.

IF 7.3 4区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Tristan Dietrich, Arthur Renaud, Gwenvael Danic, Géraldine Mineur, Guillaume Michel, Christian Lavigne, Christian Agard
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Abstract

Background: Sarcoidosis is a systemic inflammatory disease of unknown etiology. Cochleovestibular nerve involvement (CVNI) may occur as a rare manifestation of neurosarcoidosis. Comprehensive data on CVNI in neurosarcoidosis are scarce and outdated. This study aimed to provide an updated characterization of this condition.

Method: We analyzed medical records from Nantes University Hospital (2010-2023) and conducted a systematic literature review, identifying cases of neurosarcoidosis with CVNI. Data included demographics, clinical features, diagnostic findings (MRI, CSF), treatments, and outcomes.

Results: Among 39 patients (51% women, median age 40), CVNI appeared during the first flare of sarcoidosis in 90%, with hearing loss in 92%, often bilateral (78%) but rarely symmetrical (28%). Diagnostic imaging revealed internal auditory canal enhancement in 57% of cases and meningeal enhancement in 27%. CSF analysis demonstrated pleocytosis in 80% and elevated protein levels in 75%. No case had both normal MRI and CSF. Corticosteroids were used in 97%, with conventional immunosuppressants and anti-TNF-α agents in 46% and 19%, respectively. CVNI-specific improvement occurred in 59%, but only 17% achieved complete recovery. Addition of anti-TNF-α agents or conventional immunosuppressants did not improve outcomes beyond corticosteroid monotherapy.

Conclusion: CVNI in sarcoidosis is rare and diagnostically challenging. MRI and CSF analysis are key for diagnosis. Early corticosteroid treatment is essential, while additional immunosuppressive therapies offer limited short-term benefit. Prospective studies are needed to guide management.

结节病累及耳蜗前庭神经:一个病例系列和文献回顾。
背景:结节病是一种病因不明的全身性炎症性疾病。耳蜗前庭神经受累(CVNI)可能是神经结节病的罕见表现。神经结节病的CVNI的综合资料是稀缺和过时的。本研究旨在提供这种情况的最新特征。方法:我们分析南特大学医院2010-2023年的医疗记录,并进行系统的文献复习,确定神经结节病合并CVNI的病例。数据包括人口统计学、临床特征、诊断结果(MRI、CSF)、治疗和结果。结果:在39例患者中(51%为女性,中位年龄40岁),90%的患者在结节病首次发作时出现CVNI, 92%的患者伴有听力损失,通常是双侧(78%),但很少对称(28%)。诊断影像显示57%的病例有内耳道增强,27%的病例有脑膜增强。脑脊液分析显示80%的患者有细胞增多症,75%的患者蛋白水平升高。没有一例MRI和CSF同时正常。97%的患者使用皮质类固醇,46%和19%的患者使用常规免疫抑制剂和抗tnf -α药物。59%的患者出现cvni特异性改善,但只有17%的患者完全恢复。与皮质类固醇单药治疗相比,加入抗tnf -α药物或常规免疫抑制剂并没有改善预后。结论:CVNI在结节病中罕见且具有诊断挑战性。MRI和脑脊液分析是诊断的关键。早期皮质类固醇治疗是必要的,而额外的免疫抑制治疗提供有限的短期效益。需要前瞻性研究来指导管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.90
自引率
5.30%
发文量
263
审稿时长
4-8 weeks
期刊介绍: QJM, a renowned and reputable general medical journal, has been a prominent source of knowledge in the field of internal medicine. With a steadfast commitment to advancing medical science and practice, it features a selection of rigorously reviewed articles. Released on a monthly basis, QJM encompasses a wide range of article types. These include original papers that contribute innovative research, editorials that offer expert opinions, and reviews that provide comprehensive analyses of specific topics. The journal also presents commentary papers aimed at initiating discussions on controversial subjects and allocates a dedicated section for reader correspondence. In summary, QJM's reputable standing stems from its enduring presence in the medical community, consistent publication schedule, and diverse range of content designed to inform and engage readers.
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