Kaposi sarcoma (KS) is a cancerous tumor of the connective tissue.
KS is the result of infection with a herpesvirus known as Kaposi sarcoma-associated herpesvirus (KSHV), or human herpesvirus 8 (HHV8). It is in the same family as the Epstein-Barr virus, which causes mononucleosis.
KSHV is transmitted mainly through saliva. It can also be spread through sexual contact, blood transfusion, or transplants. After it enters the body, the virus can infect different kinds of cells, especially cells that line blood vessels and lymphatic vessels. Like all herpesviruses, KSHV remains in your body for the rest of your life. If your immune system becomes weakened in the future, this virus may have the chance to reactivate, causing symptoms.
There are four types of KS based on the groups of people who are infected:
- Classic KS: Mainly affects older men of Eastern European, Middle Eastern, and Mediterranean descent. The disease usually develops slowly.
- Epidemic (AIDS-related) KS: Occurs most often in people who have HIV infection and have developed AIDS.
- Endemic (African) KS: Mainly affects people of all ages in Africa.
- Immunosuppression-associated, or transplantation-associated, KS: Occurs in people who have had an organ transplant and are medicines that suppress their immune system.
The tumors (lesions) most often appear as bluish-red or purple bumps on the skin. They are reddish-purple because they are rich in blood vessels.
How KS is treated depends on:
- How much the immune system is suppressed (immunosuppression)
- Number and location of the tumors
- Antiviral therapy against HIV, since there is no specific therapy for HHV-8
- Combination chemotherapy
- Freezing the lesions
- Radiation therapy
Lesions may return after treatment.
Treating KS does not improve the chances of survival from HIV/AIDS itself. The outlook depends on the person's immune status and how much of the HIV virus is in their blood (viral load). If the HIV is controlled with medicine the lesions will often shrink away on their own.
Complications can include:
- Cough (possibly bloody) and shortness of breath if the disease is in the lungs
- Leg swelling that may be painful or cause infections if the disease is in the lymph nodes of the legs
The tumors can return even after treatment. KS can be deadly for a person with AIDS.
An aggressive form of endemic KS can spread quickly to the bones. Another form found in African children does not affect the skin. Instead, it spreads through the lymph nodes and vital organs, and can quickly become deadly.
Safer sexual practices can prevent HIV infection. This prevents HIV/AIDS and its complications, including KS.
KS almost never occurs in people with HIV/AIDS whose disease is well controlled.
Kaposi's sarcoma; HIV - Kaposi; AIDS - Kaposi
Habif TP. Vascular tumors and malformations. In: Habif TP, ed. Clinical Dermatology: A Color Guide to Diagnosis and Therapy. 6th ed. Philadelphia, PA: Elsevier; 2016:chap 23.
Kaye KM. Kaposi's sarcoma-associated herpesvirus (human herpesvirus 8). In: Bennett JE, Dolin R, Blaser MJ, eds. Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases, Updated Edition. 8th ed. Philadelphia, PA: Elsevier Saunders; 2015:chap 143.
National Cancer Institute website. Kaposi sarcoma treatment (PDQ) - health professional version. www.cancer.gov/types/soft-tissue-sarcoma/hp/kaposi-treatment-pdq. Updated July 27, 2018. Accessed December 18, 2018.
Review Date 12/1/2018
Updated by: Jatin M. Vyas, MD, PhD, Assistant Professor in Medicine, Harvard Medical School; Assistant in Medicine, Division of Infectious Disease, Department of Medicine, Massachusetts General Hospital, Boston, MA. Also reviewed by David Zieve, MD, MHA, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.