Cholesteatoma True

Cholesteatoma True: Understanding and Treatment

Cholesteatoma true (also known as congenital cholesteatoma or primary cholesteatoma) is a serious condition that can affect hearing and ear health. This pathological condition is characterized by the formation of unusual growth of epithelial tissue inside the middle ear. True cholesteatoma can destroy surrounding structures and cause serious complications, including hearing loss and infection.

True cholesteatoma usually develops as a result of a birth defect when certain structures of the middle ear do not form properly during fetal development. This can lead to the formation of a “pocket” or cyst, inside which epithelial tissue begins to actively multiply. As cholesteatoma grows, it can destroy the bones of the middle ear and spread to adjacent areas such as the inner ear or cranial cavity.

One of the first symptoms of true cholesteatoma may be recurring or chronic inflammation of the ear, accompanied by pus draining from the ear and unusual odors. Gradually, patients may notice decreased hearing, noise, or severe pain in the ear. If true cholesteatoma is left untreated, it can lead to destruction of the auditory ossicles, inner ear infections, headaches, dizziness, and even serious complications such as meningitis or brain abscess.

To diagnose true cholesteatoma, doctors usually do a comprehensive test, including audiometry to evaluate hearing and computed tomography (CT) or magnetic resonance imaging (MRI) to visualize the structures of the ear and determine the extent of the cholesteatoma.

Treatment for true cholesteatoma usually involves surgery. The purpose of the operation is to remove cholesteatoma, restore damaged ear structures and prevent recurrence. There are several surgical treatment options, including mastoidectomy, tympanoplasty, and tympanomastoidectomy. The choice of a specific procedure depends on the extent of the lesion and the individual characteristics of the patient.

After surgery, patients usually require regular medical supervision and rehabilitation measures to restore hearing and ear function. Physical therapy, audiological monitoring, and hearing aids may be recommended to help patients adjust after surgery.

True cholesteatoma is a serious disease requiring medical intervention. Early diagnosis and treatment play an important role in preventing complications and preserving the patient's hearing. If you suspect that you have true cholesteatoma or are experiencing the symptoms described above, it is important to consult an otolaryngologist for diagnosis and to determine the optimal treatment plan.

It should be noted that this article provides general information about true cholesteatoma and is not a substitute for consultation with a qualified healthcare professional. The specific approach to diagnosis and treatment may vary depending on the individual patient.

Cholestatoma is a chronic human disease, which consists of the appearance of a tumor in the area of ​​the ducts inside the head. If we talk about true cholesteatoma of the head, then this disease develops as a result of the presence of a foreign body or other obstacle to the blood flow in the body. The disease is typical for children, as well as rare cases in adults. In the practice of doctors, there are cases of the development of true cholesteatomas due to other pathologies of the body. The main provoking factors are angiomas of the spinal cord and brain. Against the background of the active course of the disease, deep complications can develop in the form of septic disease and even sepsis. Since several pathologies can provoke manifestations of a true disease at once