Neurofibromatosis is usually difficult to cure completely.
Neurofibromatosis is an autosomal dominant disorder, mainly caused by gene mutations and the presence of a family history of neurofibromatosis. Treatment is difficult and is mainly focused on improving or relieving symptoms.
Usually, neurofibromatosis type 1 can have milky coffee spots on the skin, multiple neurofibromas, freckles in the armpits and groin, intracranial tumors and other lesions, while neurofibromatosis type 2 has bilateral acoustic neuromas, tinnitus and hearing loss as the main manifestations. Treatment is based on surgical treatment and targeted therapy, but it is often difficult to cure completely due to recurrence of the disease.
When found with neurofibromatosis, it is recommended to go to the neurosurgery department of regular hospitals in time, and actively treat under the guidance of doctors to avoid delaying the condition.