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一例 Susac 综合征的颞骨表现。

Temporal bone findings in a case of Susac's syndrome.

机构信息

Johns Hopkins Hospital, Baltimore, Maryland, USA.

出版信息

Otol Neurotol. 2011 Oct;32(8):1198-204. doi: 10.1097/MAO.0b013e31822e9665.

Abstract

OBJECTIVE

To describe the histopathologic findings in the temporal bones of a patient with Susac's syndrome (SS).

BACKGROUND

The key clinical features of SS consist of symptoms of encephalopathy, visual defects due to occlusion of branches of the retinal artery, and sensorineural hearing loss. The otopathology in SS has not been described.

MATERIALS AND METHODS

A 51-year-old woman was hospitalized with severe headache, rapidly progressive encephalopathy, and bilateral low-frequency sensorineural hearing loss. Magnetic resonance imaging showed lesions of the corpus callosum. Fluorescein angiography of the eyes showed focal areas of irregular retinal artery caliber and leakage from small vessels. SS was diagnosed. She died of a pulmonary embolus 1 month after onset of symptoms. Both temporal bones were prepared in celloidin and examined using light microscopy.

RESULTS

Findings were nearly identical in both temporal bones. The apical halves of both cochleae showed widespread atrophy of structures of the cochlear duct (inner and outer hair cells, tectorial membranes, striae vasculares, spiral ligaments, and spiral limbi). The apical parts of both cochleae also showed apparent occlusion of capillaries within the stria vascularis and related areas of the cochlear duct. Cochlear neurons were present in normal numbers. There was no endolymphatic hydrops. The vestibular sense organs were normal for age.

CONCLUSION

This first reported otopathologic case of SS with hearing loss showed atrophy and degeneration involving the apical halves of the cochlear duct without inflammation or infection. The findings were consistent with capillary occlusion as being responsible for the atrophy.

摘要

目的

描述 Susac 综合征(SS)患者颞骨的组织病理学发现。

背景

SS 的主要临床特征包括脑病症状、视网膜动脉分支阻塞引起的视力缺陷和感音神经性听力损失。SS 的耳病理学尚未描述。

材料和方法

一名 51 岁女性因严重头痛、进行性脑病和双侧低频感音神经性听力损失住院。磁共振成像显示胼胝体病变。眼底荧光血管造影显示小血管的视网膜动脉口径不规则和渗漏。诊断为 SS。她在症状发作后 1 个月死于肺栓塞。对双侧颞骨进行细胞培养并使用光学显微镜检查。

结果

双侧颞骨的发现几乎相同。两个耳蜗的顶端半部显示耳蜗管结构广泛萎缩(内、外毛细胞、盖膜、血管纹、螺旋韧带和螺旋缘)。两个耳蜗的顶端部分也显示出血管纹内毛细血管和耳蜗管相关区域的明显闭塞。耳蜗神经元数量正常。无内淋巴积水。前庭感觉器官与年龄相符。

结论

首例报道的伴有听力损失的 SS 耳病理学病例显示无炎症或感染的耳蜗管顶端半部萎缩和变性。这些发现与毛细血管闭塞导致萎缩一致。

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