Is tuberous sclerosis nodosa best left untreated? Can tuberous sclerosis be treated?

Tuberous sclerosis has many manifestations, one of which is damage to the nervous system, leading to seizures. If this is the case, it can be combined with some seizure suppression medications**. However, most of the patients are children, and they should not only pursue the best effect, but should take the drug according to the characteristics of the child's own development.

Take it on time according to the doctor's instructions, and do not increase or decrease the medication according to the development of the disease. If the drug has little effect at an advanced stage, surgery** should be taken as soon as possible, such as surgery such as local cerebral cortextomy.

Another manifestation of tuberous sclerosis is the destruction of the patient's **, sebaceous adenoma will grow in the triangular area of the mouth and nose, affecting the appearance of the person, if you want to restore the appearance, you can take medical aesthetic measures to reduce the impact of sebaceous adenoma as much as possible. In addition, in daily life, we should pay attention to personal hygiene, change clothes frequently, and keep them dry and clean. Actively carry out physical exercise, increase the speed of metabolism, remove some toxins from the body, and at the same time ensure that your inner well-being, do not have too much psychological pressure, and a positive and optimistic attitude is more conducive to the recovery of the disease.

Sclerosis nodosis is a common chromosomal genetic abnormality, it is recommended that you should go to a regular hospital to receive **, under the guidance of a doctor, do not use drugs indiscriminately**, and have a reasonable diet.

Suffering from this disease, it will affect multiple organs, and there is still a lack of effective means ** disease, and it is not possible to accurately ** the course and severity of the disease, but after close monitoring and appropriate **, the patient's life span can not be affected.

It is recommended to take Chinese medicine for conditioning.

Tuberous sclerosis complex is a series of diseases caused by mutations in two genes, accounting for more than 50% of the disease. Have a hereditary, familial history of the disease. It is not necessary that two genes are mutated at the same time, as long as one gene mutation occurs, it will cause protein mutations in the body, causing the protein complex to lose its function, thereby causing overactivation of the M2 enzyme and leading to the production of diseases.

Tuberous sclerosis can generally be detected in the fetus, but because many parents do not know much about this disease, they do not do it in time, and it will cause some damage to the body after a long time. In our next article, we will introduce you to the six harms of tuberous sclerosis.

1. The first thing to damage is **. It is usually found around the age of four and appears first in the triangular region of the mouth and nose, with a butterfly-shaped symmetrical distribution and a pale red or reddish-brown color. However, as we age, our condition changes.

There are also some that will be found in the lumbosacral area over the age of ten, which will appear in the lumbosacral area, in the shape of shark skin spots, and the affected part will be higher than normal**, and the local ** will also have thickening and rough, and the color is gray-brown or slightly brown.

2. Half of the patients will have retinal glioma, which is called a lens tumor. On examination, multiple ovoid or mulberry-like calcified nodules may be found, or yellowish-white ring-shaped lesions around the periphery of the retina.

3. It can cause epilepsy, and seizures will begin in infancy. If seizures persist, it can trigger epileptic personality disorder.

4. Mental retardation, which will have mental symptoms such as emotional instability, naïve behavior, impulsivity and disordered thinking.

5. Heart disease changes, there will be cardiac rhabdomyomas, which are the largest in the neonatal period, but they will become smaller with age, and some will even disappear.

6. Osteosclerosis, this disease is generally found first in the fingers and phalanges. It can be detected by X-rays.

Tuberous sclerosis can be cured slowly. But there must be patience, it will be a long time.

Tuberous sclerosis is the best core tip: Tuberous sclerosis is a disease caused by chromosomal changes. At present, there is no way to do it, but there are some ways we can alleviate the patient's symptoms.

Tuberous sclerosis generally can't be **, most of the sclerosis nodules have chromosomal inheritance, is a kind of neurological syndrome, mainly exoculture** disease is mainly ectodermal organ development abnormality, and then involves the eyes, brain, heart, liver, lungs, peripheral nerves, kidney, bone and other organ systems, there is no very effective clinical method can be **, it is recommended that the patient is symptomatic**, if **surface pain can be applied ointment to relieve pain, if accompanied by hyperplasia can be surgically removed.

At present, tuberous sclerosis complex is more difficult, but symptomatic can improve the success rate of the disease, and in the process of tuberous sclerosis, it is necessary to maintain a calm mind and actively cooperate with the doctor.

Hello, it is more difficult to cure, and symptomatic ** can improve the quality of life of patients. Maintain a calm mind and actively cooperate**; Exercise appropriately and intensify your workout.

Tuberous sclerosis.

Tuberous sclerosis.

Synonyms: Bourneville disease.

Department: Department of Neurology.

Chen Minshan. Medical Codex Expert Group.

Chief physician of Sun Yat-sen University Cancer Prevention and Treatment Center.

Chief Physician of the Department of Liver Surgery, Sun Yat-sen University Cancer Hospital.

The content of this word is original by the Health Medical Codex, and it has been reviewed and proofread three times.

Overview**Symptom Seeker**.

Prognosis daily. **Mainly includes specificity** and synthesis**, specificity** is essential to control the progression of TSCs, mainly refers to specific targeted** drugs MTOR inhibitors.

Comprehensive ** refers to the need for a comprehensive assessment for patients with a clear diagnosis, to understand the involvement and severity of various organs, to monitor the development of the disease, and to select appropriate ** measures according to the development of the disease.

A common type of epilepsy in children with TSC. In addition to mTOR inhibitors, other antiepileptic drugs can be used, and if the response is not effective, a combination of other drugs and surgery can be considered.

Cardiac rhabdomyomas: effective with MTOR inhibitors** and requires close observation. Surgery should be considered when the tumor is large and causes significant symptoms**.

Subependymal giant cell astrocytoma: In addition to MTOR inhibitors**, some patients require surgery**.

Neurofibromas: Topical MTOR inhibitors can be used or may benefit from oral MTOR inhibitors. Other related ** are mainly considered from a cosmetic point of view.

Lymphangiomyomatosis of the lungs.

MTOR inhibitors are effective in delaying the decline in lung function and improving quality of life. Pneumothorax is predisposed to occur in concomitant lymphangiomyomatopathy.

Chylothorax. and other complications, which need to be given accordingly**.

Renal angiomyolipoma.

MTOR inhibitors**, embolization, and some surgeries are also available**. In addition, interventional embolization may be used in the presence of ruptured and hemorrhagic angiomyolipomas**.

Gingival fibroma: requires regular check-ups, good oral hygiene, and localization if necessary.

Skeletal involvement: usually no special treatment is required.

Subependymal giant cell astrocytoma.

Surgery may be considered when obstructive hydrocephalus is caused or when there is a significant mass effect**.

Tuberous sclerosis complex can involve multiple systems, and the specific hazards are as follows: 1. Brain lesions: there is subependymal giant cell astrocytoma, hydrocephalus, which is life-threatening in severe cases; 2. Seizures:

90% of patients with tuberous sclerosis have seizures, and 50% of them have intellectual disability, and epilepsy is difficult to control;

3. Ocular lesions: easy to cause retinal hamartoma, affecting vision, should be checked regularly; 4. Cardiac rhabdomyomas: small ones usually have no effect, but the larger ones or more numerous, which can easily cause abnormal myocardial contractile function, lead to arrhythmia, and even sudden death.

Tuberous sclerosis complex is an autosomal dominant disease that affects multiple systems, and there is no good way to do it so far. A specific and comprehensive approach can be taken, and rapamycin can be used as prescribed.

If seizures are induced, antiepileptic drugs such as carbamazepine should be used. Patients with subependymal giant cell astrocytoma, pulmonary lymphangiomyomatomatosis, renal angiomyolipoma and other conditions should be symptomatic**. Surgery may also be performed if necessary**.

Patients should be given more protein, vitamins and other foods rich in food. It is necessary to eat a healthy diet, participate in some outdoor sports appropriately, and also provide psychological care to patients to encourage them to build confidence in overcoming the disease.