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Vestibular system changes in sudden deafness with and without vertigo: A human temporal bone study

机译:伴或不伴眩晕的突发性耳聋的前庭系统变化:一项人类颞骨研究

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OBJECTIVE: To investigate the vestibular system changes in sudden deafness with vertigo (SDwV) and sudden deafness without vertigo (SDwoV) and the cause of persistent canal paresis (CP) in SDwV patients. STUDY DESIGN: Retrospective study. MATERIALS AND METHODS: Four temporal bones from the affected ear in 4 patients with unilateral sudden deafness (SD), 2 SDwV and 2 SDwoV, were selected. Four contralateral temporal bones with normal-hearing ears were defined as the control. Morphologic findings of the labyrinth, the number of Scarpa's ganglion cells, and the density of vestibular hair cells were investigated in all temporal bones. Clinical data and the results of vestibular tests of 11 patients with unilateral SD, as a separate group, also were investigated. RESULTS: Atrophic change of the organ of Corti, tectorial membrane, and stria vascularis in cochlea, and deposits and atrophic otoconial membrane in vestibular sense organs were seen on affected ears more than control ears. The density of Type I hair cells seemed to decrease on the saccular macula and the posterior semicircular canal crista on affected ears, and there was no remarkable difference between SDwV and SDwoV. In 1 patient with SDwoV who died 10 months after the onset of SD, there were large amount of deposits on the cupula, the atrophied otoconial membrane was peeling off from the saccular macula, and the saccular membrane collapsed to the saccular macula in the affected ear. In the clinical data, all SDwV who were examined within 2 years from the onset had CP, and all SDwV had profound hearing loss. CONCLUSION: There is no remarkable difference between SDwV and SDwoV in the number of Scarpa's ganglion cells and the density of vestibular hair cells. The damage of the extracellular superstructure is seen in SD with or without vertigo. The damage of extracellular superstructure is potentially one of the causes of persistent CP in patients with SD.
机译:目的:探讨前庭系统在患有眩晕的突发性耳聋(SDwV)和没有眩晕的突发性耳聋(SDwoV)中的变化以及SDwV患者持续性管道轻瘫(CP)的原因。研究设计:回顾性研究。材料与方法:选择4例单侧突发性耳聋(SD),2例SDwV和2例SDwoV患者患病耳朵的四个颞骨。正常耳朵的四个对侧颞骨被定义为对照组。在所有颞骨中研究迷宫的形态学发现,Scarpa神经节细胞的数量以及前庭毛细胞的密度。作为独立组,对11例单侧SD患者的临床数据和前庭检查结果进行了调查。结果:耳蜗的Corti,盖膜和血管纹的器官发生萎缩性变化,在前庭感觉器官中出现的沉积物和萎缩的耳顶膜比对耳更易见。 I型毛细胞的密度似乎在患耳的囊状黄斑和后半规管cr上减少,并且SDwV和SDwoV之间没有显着差异。在SD发病10个月后死亡的1名SDwoV患者中,在穹cup上有大量沉积物,萎缩的耳膜从囊状黄斑上剥落,并且囊状膜塌陷至患耳的囊状黄斑。在临床数据中,在发病后2年内检查的所有SDwV均患有CP,并且所有SDwV均患有严重的听力损失。结论:SDwV和SDwoV在Scarpa神经节细胞数量和前庭毛细胞密度上没有显着差异。在有或没有眩晕的SD中可见细胞外超结构的损伤。细胞外超结构的损伤可能是SD患者持续性CP的原因之一。

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