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Angiosarcoma is a rare and aggressive type of cancer that affects the blood vessels and the lining of blood vessels (endothelium) in the body. It can occur in various parts of the body, including the skin, the scalp, the breast, the liver, and the heart.
Angiosarcoma is more commonly seen in older people and in people who have been exposed to certain chemicals, such as dioxin or vinyl chloride. Other risk factors for angiosarcoma include a history of radiation exposure, lymphedema (swelling caused by a buildup of lymph fluid), and a history of other types of cancer.
Symptoms of angiosarcoma can include a rapidly growing mass or swelling, pain, bleeding, and skin discoloration.
Treatment for angiosarcoma depends on the location and stage of cancer, as well as the overall health of the patient. Treatment options can include surgery, radiation therapy, chemotherapy, and targeted therapy.
If you are experiencing symptoms that suggest angiosarcoma or have a history of risk factors for this condition, it's important to see a doctor for a diagnosis. Your doctor may perform tests such as a biopsy, a CT scan, or an MRI to diagnose angiosarcoma and determine the best course of treatment.
It's not clear what causes most angiosarcomas, though doctors have identified factors that may increase your risk of the disease.
Doctors know that something happens that causes a cell in the lining of a blood vessel or lymph vessel to develop an error (mutation) in its genetic code. The mutation tells the cell to grow quickly, making more abnormal cells. The abnormal cells continue living when other cells would die.
The result is a buildup of abnormal cells that grows from the affected blood vessel or lymph vessel. With time, cells may break off and spread (metastasize) to other areas of the body.
Which angiosarcoma treatment is best for you depends on your cancer's location, its size and whether it has spread to other areas of your body.
Treatment options may include: