What should I do if my child has neurofibromatosis?

Preface: When children are generally very young, their body resistance is relatively weak, and there are many organs that are absent, so their bodies often cause some diseases, and we can often see polio or pediatric neurofibromatosis in the vicinity. This type of illness is common and painful for children because they are not just prevented.

In particular, pediatric neurofibromas are least noticeable when the child is particularly young, such as infancy, but begin to increase after puberty.

Neurological syndromePediatric neurofibroma is a neurotic syndrome for children, it is mainly a disease caused by abnormalities in the development of the outer cortex and organs of the tissues, and usually the physical symptoms are caused by the abnormalities of the nerves and eyes. The disease usually causes other complications as well. However, according to the current level of medical research, it is not possible to clearly know the ** of these diseases, and the earliest research of doctors on this disease is that it may have some mutations when the child is embryonic in the mother's womb.

SymptomsWhen pediatric neurofibromatosis appears, we can clearly observe that the patient's ** has changed, especially some children have coffee milk spots. This symptom is an important symptom of pediatric fibromatosis. Some children are found at birth, but some do not grow until after puberty.

This milk-like form varies in size and shape on the child's body surface, and is usually a light brown coffee-like color.

In addition to the symptoms, there are usually abnormalities in the eyes and nerves, and some children's eyes can clearly see that part of their iris is not pigmented, usually a raised brown spot. At the same time, the nervous system of these pediatric fibroids is a benign tumor in the neurofibroma tissue, and the nerves in every part of the body will be implicated by this tumor. If you suffer from pediatric neurofibromas, it is mainly symptomatic**, and poor surgical results are the easiest**, so it is not suitable for surgery**.

Once such a situation occurs, it is necessary to go to a professional hospital for **, and it can also be alleviated by surgery, after the operation, you must pay attention to rest, and you must insist on taking medicine, and then you also need to control your diet, and you must pay attention to sleep.

If the child has such a disease, then it means that you should pay attention to rest, and you should protect your body, and secondly, you should go to the regular check-up to keep warm. It may generally be hereditary. And the way** is mainly symptomatic**.

The child should be taken to the hospital immediately for **, and it should be strictly ** and deployed according to the doctor's protocol, so that the child's condition can be improved.

Be sure to go to the hospital immediately**, and at the same time follow the doctor's arrangement, it is best to solve the problem through surgery.

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.

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**.