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Sudden sensorineural hearing loss: literature survey on recent studies.

机译:突然的感音神经性听力损失:有关最近研究的文献调查。

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摘要

Sudden sensorineural hearing loss (SSHL) is a symptom of cochlear injury. It is characterized by sudden onset, and, within a few hours, it reaches its maximum peak. It may be accompanied by vertigo and tinnitus. Many hypotheses have been advanced to explain its etiology: viral inflammation, vascular diseases, allergic reaction, rupture of intralabyrinthine membranes, and autoimmune diseases. The decrease in hearing may be unilateral or bilateral. To assess the histopathology of the labyrinth in cases of SSHL and to provide a better understanding of the etiopathogenesis, many studies have been carried out. Atrophy of the organ of Corti, loss of cochlear neurons, labyrinthine fibrosis, formation of new bone, and degeneration of the spiral ligament, vascular stria, hairy cells, dendrites, and apical spiral ganglion cells have been reported in temporal bone studies. In this article, new studies on the histopathologic and therapeutic bases of SSHL are reviewed.
机译:突然的感音神经性听力丧失(SSHL)是耳蜗损伤的症状。它的特征是突然发作,并在几个小时内达到最大峰值。可能伴有眩晕和耳鸣。已经提出了许多假说来解释其病因:病毒炎症,血管疾病,过敏反应,迷路内膜破裂和自身免疫性疾病。听力下降可能是单方面的或双边的。为了评估SSHL病例中迷路的组织病理学并提供对病因的更好理解,已经进行了许多研究。在颞骨研究中已报告了Corti器官的萎缩,耳蜗神经元的丧失,迷宫纤维化,新骨的形成以及螺旋韧带,血管纹,毛细胞,树突和根尖螺旋神经节细胞的变性。在本文中,综述了有关SSHL的组织病理学和治疗基础的新研究。

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