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三名重度听力损失患者颞骨中螺旋神经节和耳蜗神经的组织病理学特征。

Histopathological features of the spiral ganglion and cochlear nerve in temporal bones from three patients with profound hearing loss.

作者信息

Pollak A, Felix H

出版信息

Acta Otolaryngol Suppl. 1985;423:59-66. doi: 10.3109/00016488509122913.

Abstract

In the following study the condition of the spiral ganglion and the cochlear nerve of ears from patients suffering from profound hearing loss is described. The number of spiral ganglion cells has been related to the clinical diagnosis. The number of spiral ganglion cells in the two temporal bones of a patient with Neomycin ototoxicity was almost normal. A reduction of less than one-third of spiral ganglion cells has been observed in the temporal bones of a child who died after a bacterial labyrinthitis. The temporal bone with a Mondini dysplasia revealed a pronounced reduction of ganglion cells of more than two-thirds. The cochlear nerve trunk in the internal auditory canal appeared normal in all three cases. The present findings are discussed in respect to the degenerative behaviour of the cochlear neural elements in human being compared to animals.

摘要

在以下研究中,描述了患有严重听力损失患者耳朵的螺旋神经节和耳蜗神经的状况。螺旋神经节细胞的数量已与临床诊断相关联。一名患有新霉素耳毒性患者的两块颞骨中的螺旋神经节细胞数量几乎正常。在一名因细菌性迷路炎死亡的儿童的颞骨中,观察到螺旋神经节细胞减少不到三分之一。患有Mondini发育异常的颞骨显示神经节细胞明显减少超过三分之二。在所有三例中,内耳道中的耳蜗神经干看起来正常。就人类与动物相比耳蜗神经元的退化行为而言,对目前的研究结果进行了讨论。

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