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Congenital cholesteatoma treatment, tinnitus cure ayurvedic treatment - For Begninners

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Cholesteatomas actively erode bone because they contain enzymes which are activated by moisture. A (CAT) CT scan is obtained by the ear surgeon to determine how much the cholesteatoma has spread in the ear. Once infection is cleared up and the ear is dry, a decision regarding surgery to remove the cholesteatoma can be made.
Unless the person with cholesteatoma is extremely ill with other medical conditions, microsurgery and removal of the cholesteatoma is recommended.
A cholesteatoma usually occurs because of poor eustachian tube function as well as infection in the middle ear. An examination by an otolaryngologist—head and neck surgeon can confirm the presence of a cholesteatoma. A large or complicated cholesteatoma usually requires surgical treatment to protect the patient from serious complications. Cholesteatoma is a serious but treatable ear condition, which can be diagnosed only by medical examination. A cholesteatoma starts life as a dimple due to localised retraction of a portion of the tympanic membrane in the attic or postero superior quadrant of the pars tensa. Over time, untreated cholesteatoma can lead to bone erosion and spread of the ear infection to localized areas such as the inner ear and brain causing deafness, facial muscle paralysis, brain abscess, meningitis, and even death can occur. Cholesteatomas It usually takes the form of a cyst or pouch that containing scales of accumulated skin arranged in onion – like layers.

Ear cholesteatomas can be dangerous because of their ability to erode bone.They occur in an area crowded with important structures. Follow-up office visits after surgical treatment are necessary and important, because cholesteatoma sometimes recurs.
Initial treatment may consist of a careful cleaning of the ear, antibiotics, and ear drops. As the cholesteatoma pouch or sac enlarges, it can cause a feeling of fullness or pressure in the ear, along with hearing loss.
The term cholesteatoma is not an accurate description as it is not a tumour and always does not contain cholesterol chrystals. There is only a thin plate of bone separating a cholesteatoma from the brain and meninges and lie close to the small bones (ossicles) of the middle ear, the organ of hearing and balance in the internal ear, facial nerve. Cholesteatomas often develop as cysts or pouches that shed layers of old skin, which build up inside the middle ear. These tests are performed to determine the hearing level in the ear and the extent of destruction the cholesteatoma has caused. A second surgery is sometimes necessary both to ensure that the cholesteatoma is gone as well as to attempt reconstruction of the damaged middle ear bones in an effort to improve hearing.
In rare cases of serious infection, prolonged hospitalization for antibiotic treatment may be necessary. As the cholesteatoma pouch or sac enlarges, it can cause a full feeling or pressure in the ear, along with hearing loss.

Individuals' particular facts and circumstances will determine the treatment which is most appropriate. Over time, the cholesteatoma can increase in size and destroy the surrounding delicate bones of the middle ear leading to hearing loss that surgery can often improve.
As more and more epethilium accumulates within the bag, the cholesteatoma forms an expanding erosive bag.
Derlaki and Clemis defined congenital cholesteatoma or Primary choleasteatoma as an embryonic rest of epithelial tissue in an ear without tympanic membrane perforation, in a patient without history of ear infection. Dizziness due to involvement of the balance organ and facial muscle weakness on the same side as the cholesteatoma can occur. The primary purpose of surgery is to remove the cholesteatoma and infection and achieve an infection-free, self-cleansing dry ear. Permanent hearing loss, dizziness, and facial muscle paralysis are rare, but can result from continued cholesteatoma growth.
A rare congenital form of cholesteatoma (one present at birth) can occur in the middle ear and elsewhere, such as in the nearby skull bones. This operation will attempt to restore hearing and, at the same time, allow the surgeon to inspect the middle ear space and mastoid for residual cholesteatoma.

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Comments to “Congenital cholesteatoma treatment”

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    Drugs taken in high doses) can cause tinnitus file transformation.