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Updated: Jul 18, 2026
08:47
Endoscopic Cholesteatoma Surgery
Published on: January 19, 2022
Congenital cholesteatoma: theories, facts, and 53 patients
Marc Bennett1, Frank Warren, Gary C Jackson
1The Otology Group, Otolaryngology Head and Neck Surgery, Vanderbilt University, 300 20th Avenue North, Suite 502, Nashville, TN 37203, USA. marc.bennett@vanderbilt.edu
Otolaryngologic Clinics of North America
|November 14, 2006
Abstract:
Congenital cholesteatoma has a different pathophysiology than acquired cholesteatoma in that these patients rarely have eustachian tube dysfunction. This likely accounts for their reasonable preoperative hearing and their lack of complications or recurrences postoperatively. The most important factor is early detection. Treatment remains surgical removal.
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