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Cochlear nerve size evaluation in children with sensorineural hearing loss by high-resolution magnetic resonance imaging
被引:37
作者:
Russo, Eyal E.
Manolidis, Spiros
机构:
[1] Columbia Univ, Dept Otolaryngol, New York, NY 10032 USA
[2] Texas Childrens Hosp, Dept Otolaryngol, Houston, TX 77030 USA
关键词:
D O I:
10.1016/j.amjoto.2005.09.007
中图分类号:
R76 [耳鼻咽喉科学];
学科分类号:
100213 ;
摘要:
Purpose: To determine differences in size of cochlear nerves among subjects with deafness due to connexin 26 (Cx26) mutations, subjects with deafness of unknown origin, and normal hearing subjects by sagittal high-resolution magnetic resonance (HRMR) imaging of the temporal bone. Materials and methods: Cross-sectional and surface areas and volumetric measurements of the cochlear nerve and modiolus were made oil HRMR images of the internal auditory canal (IAC) and inner ear in the 3 groups of children (groups 1, 2, and 3). Three-way comparisons of in vivo cochlear nerve measurements oil HRMR imaging were made among 17 children with sensorineural hearing loss (SNHL) and no obvious etiology for the hearing loss (group 1), 7 children with profound SNHL due to a Cx26 mutation (group 2), and 10 normal hearing children (group 3). Results: Children with profound SNHL of unknown cause and children with profound SNHL due to a connexin Mutation displayed hypoplastic cochlear nerves as compared with normal controls. HRMR imaging of the temporal bone was accurately delineated potential problems with cochlear nerves in 2 of 17 instances where high-resolution computed tomography did not do so. Conclusions: Accurate and specific measurements of the cochlear nerve and related structures is possible oil HRMR Imaging of the temporal bone. The size of the cochlear nerve is mildly hypoplastic in children with profound SNHL of unknown causes or children with a deafness-causing Cx26 Mutation. HRMR imaging is superior to high-resolution computed tomography in the investigation of profound SNHL in children. (C) 2006 Published by Elsevier Inc.
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页码:166 / 172
页数:7
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