Literature DB >> 28446373

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

Yoshitaka Takanashi1, Tetsuaki Kawase2, Yasuko Tatewaki3, Jun Suzuki4, Izumi Yahata4, Yuuri Nomura4, Kazuha Oda4, Hiromitsu Miyazaki4, Yukio Katori4.   

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.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  3D-CT; Duplicated IAC; Inner ear malformation

Mesh:

Year:  2017        PMID: 28446373     DOI: 10.1016/j.anl.2017.03.019

Source DB:  PubMed          Journal:  Auris Nasus Larynx        ISSN: 0385-8146            Impact factor:   1.863


  1 in total

1.  De novo sensorineural hearing loss sequelae of narrow, duplicated internal auditory canal: Case series and literature review.

Authors:  Abdulaziz Saud AlEnazi; Abdulaziz Alshaiji; Meaad Alenezi; Abdulaziz Al-Sharydah; Sari Alsuhibani; Ali Alhaidey; Adnan Samarah; Munahi AlQahtani
Journal:  Int J Surg Case Rep       Date:  2022-04-20
  1 in total

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