Koç Ahmet, Sanisoğlu Orhan
Department of Otorhinolaryngology, Head and Neck Surgery, Haseki Training and Research Hospital, Istanbul, Turkey.
J Otolaryngol. 2003 Oct;32(5):308-13.
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.
突发性感音神经性听力损失(SSHL)是耳蜗损伤的一种症状。其特点是突然发病,并在数小时内达到峰值。可能伴有眩晕和耳鸣。为了解释其病因,人们提出了许多假说:病毒感染、血管疾病、过敏反应、迷路内膜破裂和自身免疫性疾病。听力下降可能是单侧或双侧的。为了评估SSHL病例中迷路的组织病理学并更好地理解其发病机制,已经开展了许多研究。颞骨研究报告了柯蒂氏器萎缩、耳蜗神经元丧失、迷路纤维化、新骨形成以及螺旋韧带、血管纹、毛细胞、树突和蜗顶螺旋神经节细胞的退变。本文综述了关于SSHL组织病理学和治疗基础的新研究。