Neurofibrosarcoma symptoms?

summary

Neurofibroma is very common in life, but many people don't know much about it. It's an infectious disease. Generally, if parents suffer from the disease, their children will have a 50% chance of developing the disease. Therefore, sterilization is generally considered for patients with the disease. Patients need to pay attention to their own conditions in daily life, Once it is found that the site of the disease is enlarged, it may be deterioration, which needs special attention. The disease is generally not completely cured, using surgical treatment, some patients may need radiotherapy, patients may have symptoms of epilepsy, this time we need to use antiepileptic drugs for treatment.

Neurofibrosarcoma symptoms?

Symptom 1: patients have more symptoms, and the symptoms in different parts are not the same. Basically, all patients with this disease will have some milk coffee spots on their skin when they are just born, and the sizes are different. When they are in childhood, they will have spots on their body and face, and the number and size are uncertain.

Symptom 2: half of the patients will have symptoms above the nervous system, mainly because the tumor compresses the central nervous system. Some intracranial tumors may lead to mental retardation or impression memory, and some patients will have symptoms of epilepsy.

Symptom 3: in addition, there will be some symptoms in the eye, some fibromas in the upper eyelid, and gray white tumors in the fundus. At the same time, some tumors may be the loss of vision, and some patients may have congenital abnormalities of bone development, which is mainly caused by tumor compression.

matters needing attention

The genetic proportion of the disease is relatively high, so for future generations need to have a certain psychological preparation, at the same time do a good job of self-examination, patients also need to actively cooperate with the treatment, according to the doctor's arrangement for activities.