Amyloidosis **common** is a form of amyloidosis, which is characterized by the presence of a large number of pathological protein deposits in various organs and tissues. Advanced amyloidosis can appear at any age and can have a variety of symptoms. Most patients with amyloidosis have a normal life expectancy, but some forms can cause disability and even death. Treatment for advanced amyloidosis may include immunosuppressive drugs, bone marrow transplantation, surgical removal of affected organs, and genetic testing. It is also important to prevent the development of symptoms of amyloid cardiomyopathy when using ACE inhibitors and angiotensin II receptor antagonists. One-time or long-term detection of signs of widespread amyolidosis is an indication for conducting a pathological examination of the tissue to detect amyloid.