Hawkins J E, Linthicum F H, Johnsson L G
Ann Otol Rhinol Laryngol Suppl. 1978 Mar-Apr;87(2 Pt 3 Suppl 48):1-40. doi: 10.1177/00034894780872s201.
In 24 temporal bones from patients with otosclerosis prepared by the method of microdissection and surface preparations, otosclerotic foci could be clearly seen during removal of the otic capsule. The state of activity of each focus was estimated on the basis of its consistency and vascularity. Small anterior foci constituted the most common form of involvement of the otic capsule. All were judged to be inactive, and none of them appeared to have caused obvious sensorineural degeneration. No cases of "pure cochlear otosclerosis" were seen. Sensorineural degeneration was associated with large anterior foci which reached the upper basal turn. One specimen displayed a circumscribed sensorineural degeneration in the upper basal turn, with an almost exact correspondence between the location and extent of the cochlear lesion and the site of invasion by the otosclerotic process in the bone and endosteum bordering on scala media and scala tympani. It is postulated that a toxic factor had diffused from the focus and acted directly on the organ of Corti. When multiple foci were present they were usually poorly defined. The otosclerotic process involved the round window, with new lamellar bone formation in the scala tympant of the lower half of the basal turn. The most extensive sensorineural degeneration in the entire material was seen in this group. One specimen also had severe cochlear hydrops. In three specimens large shunts were observed to connect the otosclerotic foci with the cochlear vasculature, which was severely dilated. Where otosclerosis involved the endosteum of the scala tympani, loss of vessels was observed. One specimum with extensive active capsular otosclerosis had severe sensorineural degeneration of the vestibular system. Vestibular pathology in fenestrated ears is also described. In a specimen from a patient with no caloric reaction, numerous hair cells were present in the macular organs.
在通过显微解剖和表面处理方法制备的24块来自耳硬化症患者的颞骨中,在去除听骨囊的过程中可以清楚地看到耳硬化病灶。根据每个病灶的质地和血管分布来评估其活动状态。小的前部病灶是听骨囊受累最常见的形式。所有这些病灶都被判定为不活跃,且似乎都未引起明显的感音神经性退变。未见到“纯耳蜗性耳硬化”病例。感音神经性退变与延伸至上基底转的大的前部病灶有关。一个标本在上基底转显示出局限性感音神经性退变,耳蜗病变的位置和范围与骨和内膜中靠近中阶和鼓阶的耳硬化过程侵袭部位几乎完全对应。据推测,一种毒性因子从病灶扩散并直接作用于柯蒂器。当存在多个病灶时,它们通常边界不清。耳硬化过程累及圆窗,在基底转下半部的鼓阶有新的板层骨形成。在整个材料中,该组出现了最广泛的感音神经性退变。一个标本还伴有严重的耳蜗积水。在三个标本中观察到有大的分流连接耳硬化病灶与严重扩张的耳蜗血管系统。当耳硬化累及鼓阶内膜时,可见血管缺失。一个有广泛活动性囊状耳硬化的标本有严重的前庭系统感音神经性退变。还描述了开窗耳的前庭病理学情况。在一个无冷热反应患者的标本中,黄斑器官中有大量毛细胞。