Yoon T H, Paparella M M, Schachern P A, Alleva M
University of Minnesota Otitis Media Research Center, Department of Otolaryngology, Minneapolis, Minnesota.
Laryngoscope. 1990 Jul;100(7):707-15. doi: 10.1288/00005537-199007000-00006.
Eleven temporal bones from eight patients who had clinical histories of sudden hearing loss (SHL) were studied to assess the possible etiopathogenesis. The origin of SHL in seven ears from five patients was obscure, but appeared to be due to multiple causes. Common histopathologic changes in the cochlea, although complex, included atrophy of the organ of Corti and loss of cochlear neurons. Loss of cochlear neurons was the main finding in ears of viral infection. Labyrinthine fibrosis and formation of new bone were seen in two ears associated with vascular insult and in two ears of autoimmune disease. Different histopathologic findings causing SHL were observed even in cases with the same etiology. A case of SHL showing endolymphatic hydrops as the main histopathologic finding is described.
对8例有突发性听力损失(SHL)临床病史患者的11块颞骨进行了研究,以评估可能的病因发病机制。5例患者7耳的SHL病因不明,但似乎是多种原因所致。耳蜗常见的组织病理学变化虽然复杂,但包括柯蒂氏器萎缩和耳蜗神经元丧失。耳蜗神经元丧失是病毒感染耳的主要发现。在与血管损伤相关的2耳以及自身免疫性疾病的2耳中可见迷路纤维化和新骨形成。即使在病因相同的病例中,也观察到了导致SHL的不同组织病理学发现。本文描述了1例以膜迷路积水为主要组织病理学发现的SHL病例。