Hello, can neurological kinoma be cured?

Neurofibromas can be performed with minimally invasive surgery, because the trauma of the operation is relatively small, and the risk factor is relatively low, so there is no need to worry too much about the risk of surgery. After surgical removal of neurofibromas, it is generally not **, and it is necessary to clean and care the incision site after surgery to avoid infection, which is easy to leave obvious scars after infection.

The disease you are talking about is a neurofibroma, an intracranial tumor, and the effect is not very ideal.

My neurofibroma grew on the left side of my face, my ears were drooping, and the bones on the left side of my face were deformed. When people grow up, this tumor is also growing, and it seems that it does not grow again when they reach adulthood. This disease is a great physical and psychological affliction.

In life, there are many beautiful things, because our abnormal body seems to really can't be a normal person.

This tumor may keep growing, and it will grow after cutting, and a girl's pregnancy may be inherited to her own child, my God, it's really miserable.

Incurable cancer, immortal cancer, see the popular science said that selumetinib has achieved phased results, I hope that this drug can be launched as soon as possible, for the majority of patients, reduce the pain, as soon as possible!

If you have actually diagnosed this disease, I believe that the doctor who gave you ** should be here after all, there are very few very complete specialties.

There is no special method for neurofibromas, neuromas in the ophthalmic nerve and auditory nerve and spinal canal can be operated on**, neurofibromas in other parts can be treated with chemotherapy and radiotherapy, in general, patients can live for a long time, epilepsy caused by neurofibromas, you can take anti-epileptic drugs, but if there are other diseases, such as hypertension or tumor lesions, etc., it will greatly reduce the life expectancy.

Neurofibromas are mainly caused by compression of central or peripheral nerve tumors, followed by gliosis, vascular hyperplasia, and skeletal deformities, and occur in about 50% of patients. Intracranial tumors, neuraxial tumors, and peripheral nerve tumors are common. Acoustic neuroma is the most common intracranial nerve tumor, and a small number of people may be affected to cause mental retardation, learning difficulties, developmental disabilities, and seizures.

Neurofibromas in the spinal canal may cause syringomyelia and spinal deformities, causing paralysis of the body and loss of superficial and deep sensations. Peripheral nerve tumors usually develop at the cauda equina at the end of the spinal nerve, and appear as bead-shaped tumors.

With the development of the disease, the symptoms and signs are varied, which can be manifested by the disease or can be regarded as a complication, easy to fracture or dislocate, when the tumor invades the central system, there may be epileptiform seizures, intracranial neurofibromas may rupture and cause intracranial hemorrhage, and huge tumors on the limbs can often rupture, leading to infection and suppuration, and even amputation. In short, having neurofibromas is very painful, and there is no good way to do it, because it is a genetic defect.

Because neurofibroma is also a kind of tumor, surgery can be performed in places where surgery can be done, and radiotherapy can be carried out in other places where surgery can not be performed to prevent benign tumor malignancy.

Neurofibromatosis is a group of diseases caused by genetic mutations, and the existing medical technology has not been able to treat them at the genetic level, and the current goal is to delay the progression of the disease as much as possible through various means and improve the quality of life of patients to the greatest extent.

Drugs**. Pain medications, such as acetaminophen and ibuprofen, are used to relieve pain caused by tumors.

Antiepileptic drugs, such as phenytoin and carbamazepine, are aimed at controlling symptoms in people with epilepsy.

Surgery**. Tumor resection: resection may be done for tumors that are large and cause severe symptoms**. For example, a craniotomy is performed to remove part or all of the tumor.

Other** methods.

Minimally invasive**:** small tumors such as laser and cryotherapy can be removed by minimally invasive surgery** such as laser and cryotherapy.

Disease development and prognosis.

If not, the associated compressive symptoms caused by the tumor may seriously affect the patient's quality of life and even lead to death.

There is currently no effective cure for the disease. Surgical resection is preferred for tumors with large growth in important parts to control local symptoms, and there is currently no effective control method for systemic symptoms. The natural history of the disease is long, and patients with neurofibromatosis type 1 generally do not affect the patient's lifespan, and some patients have malignant tumors or growth in important sites, and complications affect quality of life and longevity.

Neurofibromatosis type 2 has a poor prognosis, with residual hearing loss or complete loss after bilateral acoustic neuroma resection, and some patients may have facial paralysis, which can seriously affect life**. The survival rate of patients with multiple intracranial tumors is further reduced.

Neurofibromas are generally not completely curable. Neurofibromatosis, also known as neurofibromatosis, is an autosomal dominant disorder that is caused by abnormalities in genes and chromosomes. So far, there is no particularly effective way to do this genetic disease, and neurofibromas can appear in multiple locations.

The current best methods for neurofibromas are mainly surgery. If it is a multiple neurofibroma, then the surgical incision cannot be clean, so it cannot be **. And after surgical excision, it can reappear in other parts, so it is very difficult.

If the fibroids are very small at present, then you can not do it for the time being, you can continue to observe, and have regular reexaminations. If there are some large neurofibromas that cause symptoms that affect the nerves and compress them, they can be surgically removed. Except for surgery, there are no other effective methods, such as drugs and other conservative methods.

Neurofibromatosis cannot be complete**. Intracranial and neuraxial tumors such as acoustic neuroma and optic neuroma can be operated**, some patients can be treated with radiotherapy, and epileptic patients can be treated with antiepileptic drugs**. Pregnancy can accelerate the growth of acoustic neuroma.

Ketotifen inhibits the release of histamine from mast cells,**30 to 40 months, and some patients with itching and local tenderness symptoms can be relieved.

Quite a terrible disease, difficult to cure, the landlord should have understood, abnormal growth of body tissue, it is difficult to cure in China, and foreign scientists have developed drugs that can only be inhibited.

Hello, as long as you can find the right way**persistence** is very promising**.

Its unique cancer cell inhibitory components can increase the sensitivity of radiotherapy and chemotherapy, directly inhibit tumor cells, inhibit the generation of tumor neovascularization, and promote the transformation of cancer cells into normal cells, that is to say, make cancer cells "change from evil to right", thereby preventing the growth of tumors, and playing a role in sensitization and efficiency. In addition, it can also quickly improve the body's immune function, enhance the body's resistance, and reduce the toxicity caused by radiotherapy and chemotherapy.