ON THIS PAGE: You will find some basic information about this disease and the parts of the body it may affect. This is the first page of Cancer.Net’s Guide to Kaposi Sarcoma. Use the menu to see other pages. Think of that menu as a roadmap for this complete guide.
About Kaposi sarcoma
Cancer begins when healthy cells change and grow out of control, forming a mass called a tumor. A tumor can be cancerous or benign. A cancerous tumor is malignant, meaning it can grow and spread to other parts of the body. A benign tumor means the tumor can grow but will not spread.
Kaposi sarcoma is a type of soft-tissue sarcoma. Soft-tissue sarcomas are a group of cancers that begin in the tissues that support and connect the body.
Kaposi sarcoma generally develops in tissue located below the skin's surface or in the lining of the mouth, nose, or anus. Areas where tissues have abnormal changes are known as Kaposi sarcoma lesions. These lesions usually appear on the skin as raised blotches or nodules. They may be purple, red, blue, brown, or black. When viewed under a microscope, Kaposi sarcoma cells resemble blood vessels.
There are several types of Kaposi sarcoma:
Classic Kaposi sarcoma. Classic Kaposi sarcoma was first described in the late 1800s. It traditionally occurs in older men of Jewish or Mediterranean descent. Lesions most often appear on the lower body, particularly on the legs, ankles, or soles of the feet. Classic Kaposi sarcoma is more common in men than in women, and lesions may develop slowly over a period of 10 to 15 years.
Epidemic Kaposi sarcoma. Kaposi sarcoma in people with HIV/AIDS is often called epidemic Kaposi sarcoma. Acquired immune deficiency syndrome (AIDS) is a disease of the immune system caused by infection with the human immunodeficiency virus (HIV). It is now the most common type of Kaposi sarcoma. Epidemic Kaposi sarcoma causes lesions to form in many different areas on the body. It may affect the lymph nodes and organs, such as the liver, spleen, lungs, and the digestive tract. Learn more about HIV/AIDS-related cancer.
Acquired Kaposi sarcoma. Acquired Kaposi sarcoma develops in people whose immune systems are depressed, typically due to taking drugs to suppress their immune system in the setting of an organ transplant or an autoimmune disease. Because this treatment lowers the function of the immune system, secondary diseases or infections can occur. Kaposi sarcoma is 150 to 200 times more likely to develop in people who have received an organ transplant than in people in the general population. Most of the time, acquired Kaposi sarcoma only affects the skin, but the disease can spread to the mucous membranes or other organs.
Endemic Kaposi sarcoma. Endemic or African Kaposi sarcoma usually develops in people living in equatorial Africa. Most often, endemic Kaposi sarcoma is the same as classic Kaposi sarcoma, but people generally develop the disease at a younger age. A particularly aggressive form of endemic Kaposi sarcoma can develop in children who have not yet reached puberty. It usually involves the lymph nodes and other organs. Endemic Kaposi sarcoma usually causes skin lesions without any other symptoms, and these lesions do not spread to other parts of the body.
Looking for More of an Introduction?
If you would like more of an introduction, explore these related items. Please note that these links will take you to another section on Cancer.Net:
Cancer.Net Blog: Read an ASCO expert’s opinion about what newly diagnosed patients should know about sarcoma.
Cancer.Net Patient Education Video: View a short video led by an ASCO expert in sarcoma that provides basic information and areas of research.
The next section in this guide is Statistics. It helps explain the number of people who are diagnosed with Kaposi sarcoma and general survival rates. Use the menu to choose a different section to read in this guide.