What is the treatment for Behçet's disease?

Behcet's disease is relatively unfamiliar to many people. It is a vascular disease that usually occurs in young men and women. In the early stages of Behcet's disease, oral ulcers or skin pimples will appear. If not treated in time, it may endanger the disease. Behcet's disease should be treated early.

Effective treatment for Behcet's disease

Behcet's disease is particularly prone to relapse and can cause serious harm to the body and oral cavity. Oral ulcers caused by Behcet's disease are multiple, often involving the soft palate and oropharynx, and are extremely painful.

It starts as a "small nodule" and quickly develops into an ulcer the size of a rice grain or soybean, which is round or irregular in shape. The bottom of the ulcer may be covered with a light yellow substance and a red halo may be seen around it. At the same time, 80% of Behcet's disease patients have genital ulcers.

In addition to oral ulcers, Behcet's disease can also affect various systems throughout the body, such as the eyes, nervous system, heart, blood vessels, gastrointestinal tract, kidneys, skin, etc.

① Clearing blood clots on the inner wall of blood vessels and increasing the permeability of inflamed blood vessels can quickly block or reduce the infiltration of pathogenic fibrin and lymphocytes, allowing the ulcer surface to heal quickly.

② Clear out virus-causing toxins in the body, regulate endocrine, enhance the body's immunity and improve the antiviral ability of the mucosal keratin layer, making it less likely to relapse after recovery.

③The “naturalness” of the prescription, the “targetedness” of the treatment, and the “reliability” of the efficacy are not just in vain. It eliminates the addiction and dependence of previous antibiotics and anti-inflammatory drugs.

The cause of the disease is not fully understood at present, and may be related to genetics (such as HLA-B51 gene), infection (some patients may be related to tuberculosis infection), and living environment. It is currently believed that the pathogenesis of the disease is that the patient's immune system dysfunction occurs due to the influence of various causes, including abnormal cellular immunity and humoral immunity, hyperfunction of neutrophils, endothelial cell damage and thrombosis, and the immune system's response to its own organs and tissues, leading to inflammation and destruction of organ tissues.