What is Cholesteatoma?
Cholesteatoma is a type of noncancerous but potentially serious growth that develops in the middle ear, typically as a result of repeated ear infections or improper healing of a perforated eardrum. This abnormal skin growth can expand and erode nearby bones, leading to complications if left untreated.
Side effects of Cholesteatoma:
Cholesteatoma can cause various symptoms, including:
How is Cholesteatoma diagnosed?
Diagnosing Cholesteatoma typically involves a combination of medical history review, physical examination, and specialized tests, such as:
1. Otoscopic examination: A healthcare provider will use an otoscope to inspect the ear canal and eardrum for signs of cholesteatoma.
2. Imaging studies: CT (computed tomography) scans or MRI (magnetic resonance imaging) may be ordered to visualize the extent of the cholesteatoma and its effects on surrounding structures.
3. Hearing tests: Audiometric evaluations may be conducted to assess hearing loss associated with Cholesteatoma.
Potential treatments of Cholesteatoma:
Treatment for cholesteatoma typically involves surgery to remove the abnormal growth and prevent complications. Common surgical approaches include:
1. Tympanoplasty: This procedure repairs a perforated eardrum and removes the cholesteatoma while preserving hearing whenever possible.
2. Mastoidectomy: In cases where cholesteatoma has spread into the mastoid bone behind the ear, a mastoidectomy may be necessary to remove affected tissue and prevent recurrence.
3. Ossiculoplasty: If cholesteatoma has damaged the small bones of the middle ear (ossicles), reconstructive surgery may be performed to restore hearing.
4. Canal wall-up or canal wall-down procedures: These surgical techniques involve either preserving or removing part of the ear canal wall, depending on the extent of cholesteatoma and the desired outcome.
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