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Published on: December 15, 2023
Pediatric Congenital External Auditory Canal Cholesteatoma Extending Beyond the External Auditory Canal: A Case
Kohei Yamahara1, Takayuki Okano2, Kana Sano1
1Department of Otolaryngology-Head and Neck Surgery, School of Medicine, Fujita Health University, Toyoake, JPN.
Insights
This study details a rare pediatric congenital external auditory canal cholesteatoma (EACC) case extending into the mastoid. We propose features to differentiate congenital from acquired EACC, aiding diagnosis and treatment.
Area of Science:
- Otolaryngology
- Pediatric Surgery
- Medical Imaging
Background:
- Congenital external auditory canal cholesteatoma (EACC) is rare, with increasing pediatric reports.
- Distinguishing congenital from acquired EACC is challenging, especially in advanced stages.
Abstract:
This article describes an extremely rare case of pediatric congenital external auditory canal cholesteatoma (EACC) that extended beyond the external auditory canal. A five-year-old girl presented with progressive swelling in the posterior wall of the left external auditory canal. Computed tomography of the temporal bone revealed a well-defined round mass that compressed and eroded the posterior canal wall without invasion of the mastoid tegmen, sigmoid sinus, or tympanic membrane. Surgical exploration via a retroauricular approach confirmed the presence of a cholesteatoma extending from the external auditory canal to the mastoid cavity; furthermore, complete excision was achieved. There has been a recent increase in the number of reported EACC pediatric cases, especially in East Asia. However, few studies have clearly distinguished congenital and acquired forms, which could be largely attributed to challenges in differential diagnosis, particularly when lesions extend beyond the canal. Based on our findings, we propose radiological and clinical features that may facilitate differentiation between congenital and acquired EACC, even in advanced-stage cases. This article highlights the importance of accurate classification for elucidation of the pathogenesis of EACC and optimization of surgical decision-making in pediatric patients with EACC.

