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External auditory canal cholesteatoma is rare (incidence 1.2 per 1,000 otological patients) compared to middle ear cholesteatoma (9.2 per 100,000 inhabitants annually).
Primary cholesteatoma (idiopathic/spontaneous) is rare; secondary forms follow otologic surgery, inflammation, trauma, or radiation to the external canal.
The distinction from keratosis obturans is clinically important because it determines treatment strategy: keratosis obturans may respond to conservative management, while cholesteatoma requires surgical removal of bone and epithelial debris.
Stage of disease at presentation significantly impacts prognosis and treatment approach, ranging from endoscopic management of small lesions under local anesthesia to formal surgical excision with bone removal and potential grafting for larger or advanced-stage lesions.
Report the precise location and extent of the soft tissue density lesion within the external auditory canal, clearly describe any focal osteonecrosis or bone sequestration, classify the stage (I–IV) based on extension into tympanic membrane/middle ear/mastoid/beyond temporal bone), and note the degree of canal wall erosion to guide surgical planning.