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Duplicated internal auditory canal with inner ear malformation: Case report and literature review.

Authors :
Takanashi Y
Kawase T
Tatewaki Y
Suzuki J
Yahata I
Nomura Y
Oda K
Miyazaki H
Katori Y
Source :
Auris, nasus, larynx [Auris Nasus Larynx] 2018 Apr; Vol. 45 (2), pp. 351-357. Date of Electronic Publication: 2017 Apr 23.
Publication Year :
2018

Abstract

Internal auditory canal anomalies are rare. Narrow internal auditory canal is believed to occur as a result of aplasia or hypoplasia of the vestibulocochlear nerve. Narrow duplication of the internal auditory canal is considered to be very rare. Narrow duplication of the internal auditory canal with inner ear malformation has been reported in only 3 cases. We present 2 cases of narrow duplication of the internal auditory canal with inner ear malformation. The first case had inner ear malformation on only one side and the second case had inner ear malformation on both sides. The embryogenesis may be different between internal auditory canal and inner ear.<br /> (Copyright © 2017 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1879-1476
Volume :
45
Issue :
2
Database :
MEDLINE
Journal :
Auris, nasus, larynx
Publication Type :
Academic Journal
Accession number :
28446373
Full Text :
https://doi.org/10.1016/j.anl.2017.03.019