РАННЯЯ ДИАГНОСТИКА СИСТЕМНОЙ СКЛЕРОДЕРМИИ

Аннотация

Systemic scleroderma (TSD) is an autoimmune disease based on the activity of fibrosis processes in the skin and internal organs, as well as general microangiopathy. In the initial bandages, the disease is manifested by uzini edema of the chest in the fingers and skin changes in the course of the rhinitis syndrome, but the patient may not have any manifestations of deterioration of the general condition or signs of damage to internal organs (dysphagia, iaphasic stenosis, etc.), so the patient can get an early referral to a doctor in In this regard, systemic scleroderma is diagnosed with a delayed diagnosis, after the appearance of irreversible pathological changes in the organs and finding the treatment ineffective in the body. According to Canadian researchers, a diagnosis of systemic sclerodermia in 408 bsmor was made after 6.0 years of uttering and 2.7 years of uttering of primary "skin manifestations" had appeared [21J. In Russia, systemic scleroderma is diagnosed when the disease is 2,0-2,7 years old from the syndrome of the Rhine, and in diffuse and limited forms of the disease 4,8-6,5 years old when the diagnosis is found burn, which is associated with a variety of degree of damage to internal organs, as well as with the speed of At the same time, the results of a large study show that the incidence of bsmor with this disease is 68 out of 1000 patients per year [36]. So the diagnosis of weight loss and systemic sclerodermia in uz vaccine is a complex, but very sparing task for the doctor.