A pathologic, chronic inflammatory process characterized by the accumulation of keratinizing squamous epithelium, resulting in the accumulation of debris in the middle ear and/or mastoid. It may be congenital but is more commonly acquired. If left untreated, it may increase in size and destroy adjacent structures, resulting in hearing loss, facial paralysis, and less commonly, intracranial complications. Treatment is surgical removal. Patients who have had cholesteatoma removal surgery require lifelong monitoring of their ears for recurrence.
See also cholesteatoma of middle ear and cholesteatoma of external ear.
Cholesteatoma
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Synopsis
Codes
ICD10CM:
H71.93 – Unspecified cholesteatoma, bilateral
SNOMEDCT:
363668000 – Cholesteatoma
H71.93 – Unspecified cholesteatoma, bilateral
SNOMEDCT:
363668000 – Cholesteatoma
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Last Updated:01/12/2022
Cholesteatoma