Evaluation of Growth and Development of the External Auditory Canal Using 624 Temporal Bone Computed Tomography Scans

Kazuki Matsuura1, Hidekane Yoshimura1, Yoshinori Tsukahara2

  • 1Department of Otorhinolaryngology - Head and Neck Surgery.

Abstract

Insights

Pediatric external auditory canal (EAC) anatomy significantly changes in the first year of life. For cochlear gene therapy in infants under one, a transmastoid approach is recommended over transcanal due to narrow EAC dimensions.

Area of Science:

  • Otolaryngology
  • Pediatric Surgery
  • Medical Imaging

Background:

  • Cochlear gene therapy for autosomal recessive deafness 9 utilizes transcanal and transmastoid approaches.
  • Transcanal endoscopic approaches may be limited in young children due to small external auditory canal (EAC) size.
  • Evaluating pediatric EAC anatomy is crucial for surgical planning.

Purpose of the Study:

  • To assess pediatric external auditory canal (EAC) anatomy using temporal bone computed tomography (CT).
  • To determine the feasibility of transcanal endoscopic approaches in pediatric patients.
  • To inform surgical approach selection for cochlear gene therapy in children.

Main Methods:

  • Retrospective analysis of 624 temporal bone CT scans from children aged 0-18 years.
  • Detailed measurements of EAC dimensions, including lengths, angles, and diameters.
  • Standardized assessment method applied to all CT scans.

Main Results:

  • Significant increases in EAC length and diameter observed between 0 and 1 year of age.
  • Annual increases in key measurements: 2.21 mm (inferior wall length), 8.59 mm (bony wall length), 33.0 degrees (angle), and 1.43 mm (narrowest diameter).
  • Tympanic membrane diameter remained constant throughout childhood.

Conclusions:

  • Transcanal endoscopic ear surgery feasibility is dependent on EAC narrowest point diameter and bony length.
  • A transmastoid microscopic approach is recommended for patients under 1 year of age.
  • Findings guide surgical approach selection for pediatric cochlear gene therapy.

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