Nelson E G, Hinojosa R
Section of Otolaryngology-Head and Neck Surgery, University of Chicago Medical Center, 5841 S. Maryland Avenue, MC 1035, Chicago, IL 60637, USA.
Otol Neurotol. 2001 Nov;22(6):790-5. doi: 10.1097/00129492-200111000-00013.
The purpose of this study was to evaluate the temporal bone findings in individuals with cochlear nerve aplasia.
Retrospective case review.
Two individuals with unilateral profound deafness caused by aplasia of the cochlear nerve were identified. The temporal bones were processed, and the cochlear elements were quantified.
Histopathologic study of the temporal bones from these individuals demonstrate that a fully formed cochlea and normal-appearing organ of Corti can occur in the absence of the spiral ganglion and cochlear nerve. Cochlear nerve aplasia can occur in both a narrow or a normal-sized internal auditory canal.
These findings suggest that the development of the cochlea and organ of Corti are not dependent on the presence of the cochlear nerve and spiral ganglion. The entity of cochlear nerve aplasia in the presence of a normally formed cochlea must be considered when evaluating individuals as candidates for cochlear implantation.
本研究旨在评估耳蜗神经发育不全个体的颞骨表现。
回顾性病例分析。
确定了两名因耳蜗神经发育不全导致单侧重度耳聋的个体。对颞骨进行处理,并对耳蜗结构进行量化。
对这些个体颞骨的组织病理学研究表明,在没有螺旋神经节和耳蜗神经的情况下,可出现完全形成的耳蜗和外观正常的柯蒂器。耳蜗神经发育不全可发生于狭窄或正常大小的内耳道。
这些发现表明,耳蜗和柯蒂器的发育不依赖于耳蜗神经和螺旋神经节的存在。在评估个体是否适合人工耳蜗植入时,必须考虑在耳蜗正常形成的情况下出现耳蜗神经发育不全的情况。