Hemoderma Nonspecific

Nonspecific hemoderma (syn. leukemides) is a group of blood diseases that are characterized by the presence of a large number of leukocytes in the blood. These diseases can be caused by various reasons such as infections, autoimmune diseases, chemicals and other factors.

Nonspecific hemoderma can manifest as a variety of symptoms, including fever, fatigue, joint and muscle pain, and changes in blood tests. Treatment depends on the cause of the disease and may include antibiotics, anti-inflammatory drugs and other treatments.

It is important to note that nonspecific hemoderma is a serious disease that can lead to serious complications such as sepsis and infections. Therefore, if you notice any symptoms of this disease, you should consult a doctor for diagnosis and treatment.

Nonspecific hemoderma is a blood disease of a malignant nature.

In nonspecific hemoderma, tumor cells do not have connections with specific organs or tissues, but are distributed throughout the body and divide equally actively. In children, hemoderma appears after 2 years, in adults the first signs are from puberty to 35-40 years. Hemoderma is diagnosed when a tumor of the bone tissue of the periosteum or the bone itself penetrates into the blood. Having penetrated the blood, the tumor begins to separate, so it can spread through the bloodstream throughout the body. Diseases occur rarely, but mortality in some cases reaches 80%.