My child was diagnosed with neurofibroma

This is a benign tumor, but there is still a chance of local **, local resection, local observation and treatment can be done.

A single neurofibroma can be removed if it is not a major problem.

Surgery can be used to remove the excision, and regular re-examinations can be done.

Parents should be vigilant and consider neurofibromatosis.

Neurofibromatosis accounts for neonatal disease and is characterized by multiple tumors of the nervous system, café-au-lait spots, and other organ tumors.

Parents should also pay attention to the presence of neurofibromas when they see ** café au lait spots. This type of tumor is as small as a needle, as large as a grape, soft in texture, pedicle or sessile, or brown or red or consistent with the color of **, the number varies, and it is commonly found on the trunk, limbs or scalp.

About half of the affected children have neurological symptoms, which vary depending on where the tumor grows. In younger children, there are often single intracranial tumors, such as acoustic neuroma, optic neuroma, etc.; Older children may have neuraxial tumors.

Parents may also see that the child has seizures, mental retardation, and speech and motor delays. Other organs are also affected.

Parents should think of this disease as soon as they find that there are more café au lait spots, and immediately take the sick child to the doctor for a detailed physical examination and neurological examination.

The disease is mainly symptomatic**, but it can also be operated or radiated**.

Hello, neurofibroma features are as follows:

1. **Café au lait spots appear.

2. Most of the tumors are located in the limbs and armpits, but also in the clavicle, neck and other parts.

3. The tumor located on the limb is fusiformal, and the distal limb innervated by the nerve trunk often has symptoms such as numbness, pain, and hyperesthesia.

4. Compression of the tumor can also cause numbness.

If you have any of the above symptoms, you must actively go to the hospital for examination. If confirmed, it must be positive**. Preamble tumor--Kang-fu can be used'- Scattered, can improve the quality of life of patients, cure.

The rate is high, and'Vice''It has little effect and is an ideal drug for the treatment of neurofibroids.

Neurofibromas are non-hereditary diseases. It's like a cold, he doesn't have to catch a cold, you also catch a cold. Don't worry too much, this is generally a benign tumor, as long as it is not in the critical area, it is better to go to a regular hospital for removal as soon as possible.

As the disease progresses, symptoms and signs appear in a variety of ways, ranging from the disease to complications.

1. Fracture or dislocation: When the tumor invades the skeletal system, it can cause fractures, dislocations, spinal deformities, scoliosis, congenital tibial pseudojoint and congenital clavicle pseudojoint. When a tumor compresses the common peroneal nerve, it can cause foot drop.

2. Epilepsy: When the tumor invades the central system, there may be epileptiform seizures, and attention should be paid to prevent trauma.

3. Neurofibromas can sometimes break down and bleed on their own, or they can cause massive bleeding inside the tumor, and in severe cases, they can cause shock.

4. Huge tumors on limbs can often rupture, leading to infection and suppuration, and even amputation.

5. Lung damage: a small number of patients can develop diffuse interstitial pneumonia.

6. Malignant tumors: **Neurofibromas can occasionally develop into neurofibrosarcoma and malignant schwannoma. Patients with WILM tumors, striated muscle tumors and chronic myeloid leukemia have also been reported.

Immunity will continue to decline, resistance will continue to decline, and the functions in the body will continue to decline, if the situation is very serious, it will affect the safety of life, and it will also make the child's body continue to appear abnormal, and it will also make the child's body lack a lot of trace elements. Therefore, when the child has this situation, it must be timely and do not bring unnecessary trouble to the child.

**The color will change, and there will be some coffee-colored spots on the face, the number will increase, and it will be stunted, there will be some abnormalities in the eyes, and there will be abnormalities in the nervous system, which will lead to membranous tubeoma.

In the later stage, it will appear unresponsive, the color of ** will change, vision will decrease, eye abnormalities, sluggish movements and other symptoms, so we must pay attention.