CLINICAL CASE SYSTEMIC SCLERODERMA A MIDDLE-AGED WOMAN

Abstract

Systemic scleroderma is a rare chronic disease characterized by the development of diffuse fibrosis, pathological changes in the skin, blood vessels, joints and internal organs. The article presents a clinical case of a patient with systemic scleroderma with such obvious manifestations of skin and vascular lesions as sclerodactyly, masking of the face, "purse-string mouth", Raynaud's syndrome, as well as lesions of the joints, muscles, immunological disorders, the development of steroid osteoporosis with multiple fractures