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Cholesteatoma therapy involves the surgical removal of an abnormal skin cell collection in the middle ear. The goal is complete elimination of the lesion and preservation of hearing.
Cholesteatoma therapy involves the surgical removal of an abnormal skin cell collection in the middle ear. The goal is complete elimination of the lesion and preservation of hearing.
A cholesteatoma is a benign but locally destructive accumulation of squamous epithelium (keratinized skin cells) within the middle ear or petrous bone. Despite its name, it is not a true tumor but rather an abnormal growth of skin tissue in a location where it does not normally occur. If left untreated, a cholesteatoma can erode surrounding bone, the ossicular chain, and even structures of the inner ear or skull base.
Cholesteatomas are classified as either primary (congenital) or secondary (acquired):
Typical signs and symptoms of a cholesteatoma include:
Diagnosis is established through otoscopic examination of the ear canal and eardrum, supplemented by imaging studies such as CT (computed tomography) or MRI (magnetic resonance imaging) of the temporal bone to assess the extent of disease and detect potential complications.
Surgical removal is the only effective treatment for a cholesteatoma. Conservative or medication-based approaches cannot stop its growth and are used only to control infection prior to the operation.
The choice of surgical technique depends on the size, location, and extent of the cholesteatoma:
For extensive lesions, a staged (two-stage) surgical approach is often chosen: the cholesteatoma is removed in the first operation, while reconstruction of the ossicular chain (ossiculoplasty) is performed in a second procedure approximately 6 to 12 months later. This allows the surgeon to check for residual or recurrent disease before committing to final reconstruction.
Regular follow-up examinations with an ENT specialist are essential after surgery, as cholesteatomas have a recurrence rate of up to 30%. In addition to clinical checks, non-echo-planar diffusion-weighted MRI is increasingly used to detect residual or recurrent cholesteatoma non-invasively, avoiding the need for immediate revision surgery.
Untreated cholesteatomas can lead to serious complications, including:
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