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Keratosis obturans is characterized by abnormal accumulation of desquamated keratin within the deep meatus leading to progressive expansion and remodeling of the bony external auditory canal without erosion, distinguishing it from erosive pathology like cholesteatoma.
The condition is bilateral in 50% of cases and strongly associated with bronchiectasis and chronic paranasal sinus disease in up to 80% of pediatric patients but only 20% of adult patients, suggesting underlying airway pathology may be contributory.
The dense keratin plug causes conductive hearing loss and acute severe pain due to occlusion of the canal, requiring treatment by EAC toilet rather than major surgery.
High recurrence rate necessitates multiple excisions of keratin plugs, making imaging follow-up important to assess for recurrent accumulation and canal expansion.
Unlike cholesteatoma, keratosis obturans does not erode bone and typically does not require surgical intervention, making accurate diagnosis essential to avoid unnecessary ear canal surgery.
Describe keratosis obturans as a well-defined soft tissue mass densely filling and expanding the bony external auditory canal without erosion, with preserved tympanic membrane, and specify presence or absence of bilateral involvement and associated paranasal sinus or lung findings to guide clinical management toward conservative EAC toilet rather than surgery.