Yaku Y, Komatsuzaki A
Department of Otolaryngology, Head and Neck Surgery, Tochigi Cancer Center, Japan.
Am J Otolaryngol. 1989 Sep-Oct;10(5):336-41. doi: 10.1016/0196-0709(89)90109-9.
Vestibular sensory organs were examined ultrastructurally in two cases of delayed endolymphatic hydrops. The patients, two women, 27 and 16 years of age, suffered profound sensory hearing loss in childhood and experienced severe, recurrent vertigo. Specimens were obtained by a translabyrinthial vestibular nerve transection. We studied the utricular macula and the lateral and posterior cristae in one case, and the utricular macula, the anterior and posterior cristae, and the vestibular ganglion in the other. The otoconia and the otoconial membrane, the sensory epithelia, and the vestibular ganglion appeared fairly normal. Although the entire vestibular end organs were not studied in these cases, it was surprising that the ultrastructural findings did not conclusively identify vestibular end organ pathology as the cause of the vertigo attacks.
对两例迟发性内淋巴积水患者的前庭感觉器官进行了超微结构检查。患者为两名女性,年龄分别为27岁和16岁,童年时患有严重的感音神经性听力损失,并经历严重的复发性眩晕。标本通过经迷路前庭神经切断术获取。我们在一例中研究了椭圆囊斑以及外侧和后嵴,在另一例中研究了椭圆囊斑、前嵴和后嵴以及前庭神经节。耳石和耳石膜、感觉上皮以及前庭神经节看起来基本正常。尽管在这些病例中没有对整个前庭终器进行研究,但令人惊讶的是,超微结构检查结果并未明确确定前庭终器病变是眩晕发作的原因。