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浅表性铁沉积症中的双侧前庭病

Bilateral Vestibulopathy in Superficial Siderosis.

作者信息

Lee Sang-Yeon, Lee Dong-Han, Bae Yun Jung, Song Jae-Jin, Kim Ji Soo, Koo Ja-Won

机构信息

Department of Otorhinolaryngology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, South Korea.

Department of Radiology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, South Korea.

出版信息

Front Neurol. 2018 Jun 6;9:422. doi: 10.3389/fneur.2018.00422. eCollection 2018.

Abstract

Superficial siderosis (SS) is a rare condition in which hemosiderin, an iron storage complex, is deposited in neural tissues because of recurrent subarachnoid bleeding. Hemosiderin deposition in the vestibulocochlear nerve (CN VIII), brain, spinal cord and peripheral nerve can cause sensorineural hearing loss (SNHL) and postural imbalance, but much remains unknown about the vestibular manifestations of SS. To report the clinical course, cochleovestibular status, and patterns of vestibulopathy during follow-up of a relatively large case series, and to discuss the possible pathophysiological mechanism of vestibular deterioration. Six patients diagnosed with SS by magnetic resonance imaging (MRI) were enrolled. Their medical records and radiological findings were retrospectively reviewed, particularly in terms of progression of the vestibulocochlear manifestations and the radiological characteristics. All six patients had SNHL. Five of them exhibited progressive hearing loss over years, which was asymmetric in four. On their most recent evaluations, patients showed cerebellar ataxia with combined central and peripheral vestibulopathy on both sides ( = 4), a bilateral peripheral vestibulopathy ( = 1) or isolated central vestibulopathy ( = 1). Notably, the former four patients showed an evolution of isolated central vestibulopathy into combined central and peripheral vestibulopathy. Hypo-intense lesions on T2 weighted MRIs were evident around the cerebellum in all patients, but such lesions were observed around the brainstem in five and the CN VIII in four. The cochlea-vestibular dysfunction generally progressed asymmetrically, but no left-right asymmetry was evident on MRI. SS typically presents as bilaterally asymmetric, progressive cochleovestibular dysfunction with cerebellar ataxia. The pattern of vestibular dysfunction is usually combined central and peripheral vestibulopathy on both sides. Thus, precise identification of audiovestibular dysfunction and central signs is essential in SS, and patients with SS should undergo regular, comprehensive neurotological evaluation to optimize their treatments and prognosis.

摘要

浅表性铁沉积症(SS)是一种罕见病症,由于反复蛛网膜下腔出血,铁储存复合物含铁血黄素沉积于神经组织。含铁血黄素在前庭蜗神经(第八对脑神经)、脑、脊髓和周围神经的沉积可导致感音神经性听力损失(SNHL)和姿势失衡,但关于SS的前庭表现仍有许多未知之处。报告一个相对较大病例系列随访期间的临床病程、耳蜗前庭状态和前庭病变模式,并探讨前庭功能恶化可能的病理生理机制。纳入6例经磁共振成像(MRI)诊断为SS的患者。对他们的病历和影像学检查结果进行回顾性分析,尤其关注前庭蜗表现的进展情况和影像学特征。所有6例患者均有SNHL。其中5例多年来听力呈进行性下降,4例为不对称性下降。在最近一次评估中,患者表现为双侧合并中枢性和外周性前庭病变的小脑共济失调(4例)、双侧外周性前庭病变(1例)或孤立性中枢性前庭病变(1例)。值得注意的是,前4例患者表现为从孤立性中枢性前庭病变演变为合并中枢性和外周性前庭病变。所有患者在T2加权MRI上小脑周围均可见低信号病变,但5例在脑干周围、4例在前庭蜗神经周围也观察到此类病变。耳蜗前庭功能障碍通常呈不对称性进展,但MRI上未发现明显的左右不对称。SS通常表现为双侧不对称、进行性耳蜗前庭功能障碍并伴有小脑共济失调。前庭功能障碍模式通常为双侧合并中枢性和外周性前庭病变。因此,准确识别SS患者的听前庭功能障碍和中枢性体征至关重要,SS患者应定期接受全面的神经耳科学评估,以优化治疗和预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d6a/5997823/0bba54e1d086/fneur-09-00422-g0001.jpg

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