++
Despite their name, cholesteatomas are not composed of cholesterol, nor are they a form of a malignancy. Cholesteatomas are collections of desquamating stratified squamous epithelium found in the middle ear or mastoid air cells. Congenital cholesteatomas occur most frequently in children and young adults. Acquired cholesteatomas originate from perforation or retraction of the TM allowing migration of epithelium into the middle ear.
++
Injury may occur to middle ear ossicles through the production of collagenases and may erode into the temporal bone, inner ear structures, mastoid sinus, or posterior fossa dura. Treatment delays can lead to permanent conductive hearing loss or infectious complications.
++
Many cholesteatomas have an insidious progression without associated pain or symptoms. Computed tomography (CT) scans may reveal bony destruction.
+++
Management and Disposition
++
Refer to otorhinolaryngology (ENT) upon initial diagnosis. No emergent medical or surgical management is required unless they become symptomatic.
++
Persistent pain associated with headache, facial motor weakness, nystagmus, or vertigo suggests inner ear or intracranial involvement.
Polyps found on the TM may indicate the presence of a cholesteatoma and require further evaluation to exclude its presence.
++++++