Childhood vascular tumors form from cells that make blood vessels or lymph vessels.

Vascular tumors can form from abnormal blood vessel or lymph vessel cells anywhere in the body. They may be benign (not cancer) or malignant (cancer). There are many types of vascular tumors. The most common type of childhood vascular tumor is infantile hemangioma, which is a benign tumor that usually goes away on its own.

Because malignant vascular tumors are rare in children, there is not a lot of information about what treatment works best.

Tests are used to detect (find) and diagnose childhood vascular tumors.

The following tests and procedures may be used:

• Physical exam and history: An exam of the body to check general signs of health, including checking for signs of disease, such as lumps, lesions, or anything else that seems unusual. A history of the patient’s health habits and past illnesses and treatments will also be taken.
• Ultrasound exam: A procedure in which high-energy sound waves (ultrasound) are bounced off internal tissues or organs and make echoes. The echoes form a picture of body tissues called a sonogram. The picture can be printed to be looked at later.

  

  Abdominal ultrasound. An ultrasound transducer connected to a computer is pressed against the skin of the abdomen. The transducer bounces sound waves off internal organs and tissues to make echoes that form a sonogram (computer picture).

• CT scan (CAT scan): A procedure that makes a series of detailed pictures of areas inside the body, taken from different angles. The pictures are made by a computer linked to an x-ray machine. A dye may be injected into a vein or swallowed to help the organs or tissues show up more clearly. This procedure is also called computed tomography, computerized tomography, or computerized axial tomography.

  

  Computed tomography (CT) scan of the abdomen. The child lies on a table that slides through the CT scanner, which takes x-ray pictures of the inside of the abdomen.

• MRI (magnetic resonance imaging): A procedure that uses a magnet, radio waves, and a computer to make a series of detailed pictures of areas inside the body. This procedure is also called nuclear magnetic resonance imaging (NMRI).

  

  Magnetic resonance imaging (MRI) of the abdomen. The child lies on a table that slides into the MRI scanner, which takes pictures of the inside of the body. The pad on the child’s abdomen helps make the pictures clearer.

• Biopsy: The removal of cells or tissues so they can be viewed under a microscope by a pathologist to check for signs of cancer. A biopsy is not always needed to diagnose a vascular tumor.

Childhood vascular tumors may be classified into four groups.

There are different types of treatment for childhood vascular tumors.

Different types of treatment are available for children with vascular tumors. Some treatments are standard (the currently used treatment), and some are being tested in clinical trials. A treatment clinical trial is a research study meant to help improve current treatments or obtain information on new treatments. When clinical trials show that a new treatment is better than the standard treatment, the new treatment may become the standard treatment.

Because vascular tumors in children are rare, taking part in a clinical trial should be considered. Some clinical trials are open only to patients who have not started treatment.

Children with childhood vascular tumors should have their treatment planned by a team of health care providers who are experts in treating cancer in children.

Treatment will be overseen by a pediatric oncologist, a doctor who specializes in treating children with cancer. The pediatric oncologist works with other pediatric health care providers who are experts in treating children with cancer and who specialize in certain areas of medicine. These may include the following specialists:

• Pediatric vascular anomaly specialist (expert in treating children with vascular tumors).
• Pediatric surgeon.
• Orthopedic surgeon.
• Radiation oncologist.
• Pediatric nurse specialist.
• Rehabilitation specialist.
• Psychologist.
• Social worker.

Some treatments cause side effects months or years after treatment has ended.

Some treatments, such as chemotherapy and radiation therapy, cause side effects that continue or appear months or years after treatment has ended. These are called late effects. Late effects of treatment may include:

• Physical problems.
• Changes in mood, feelings, thinking, learning, or memory.
• Second cancers (new types of cancer).

Some late effects may be treated or controlled. It is important to talk with your child's doctors about the possible late effects caused by some treatments. (See the PDQ summary on Late Effects of Treatment for Childhood Cancer for more information).

Eleven types of standard treatment are used:

New types of treatment are being tested in clinical trials.

Information about clinical trials is available from the NCI website.

Patients may want to think about taking part in a clinical trial.

For some patients, taking part in a clinical trial may be the best treatment choice. Clinical trials are part of the research process. Clinical trials are done to find out if new treatments are safe and effective or better than the standard treatment.

Many of today's standard treatments are based on earlier clinical trials. Patients who take part in a clinical trial may receive the standard treatment or be among the first to receive a new treatment.

Patients who take part in clinical trials also help improve the way disease will be treated in the future. Even when clinical trials do not lead to effective new treatments, they often answer important questions and help move research forward.

Patients can enter clinical trials before, during, or after starting their cancer treatment.

Some clinical trials only include patients who have not yet received treatment. Other trials test treatments for patients whose tumors have not gotten better. There are also clinical trials that test new ways to stop tumors from recurring (coming back) or reduce the side effects of treatment.

Clinical trials are taking place in many parts of the country. Information about clinical trials supported by NCI can be found on NCI’s clinical trials search webpage. Clinical trials supported by other organizations can be found on the ClinicalTrials.gov website.

Follow-up tests may be needed.

Some of the tests that were done to diagnose the vascular tumor may be repeated. Some tests will be repeated in order to see how well the treatment is working. Decisions about whether to continue, change, or stop treatment may be based on the results of these tests.

Some of the tests will continue to be done from time to time after treatment has ended. The results of these tests can show if your child's condition has changed or if the tumor has recurred (come back). These tests are sometimes called follow-up tests or check-ups.

Infantile Hemangioma

Infantile hemangiomas are the most common type of benign vascular tumor in children. Infantile hemangiomas form when immature cells that are meant to form blood vessels form a tumor instead. An infantile hemangioma may also be called a "strawberry mark."

These tumors are not usually seen at birth but appear when the infant is 3 to 6 weeks old. Most hemangiomas get bigger for about 5 months and then stop growing. The hemangiomas slowly fade away over the next several years, but a red mark or loose or wrinkled skin may remain. It is rare for an infantile hemangioma to come back.

Infantile hemangiomas may be on the skin, in the tissue below the skin, and/or in an organ. They are usually on the head and neck but can be anywhere on or in the body. Hemangiomas may appear as a single lesion, one or more lesions spread over a larger area of the body, or multiple lesions in more than one part of the body. Lesions that are spread over a larger area of the body or multiple lesions are more likely to cause problems.

Risk Factors

Anything that increases your risk of getting a disease is called a risk factor. Having a risk factor does not mean that you will get the disease; not having risk factors doesn’t mean that you will not get the disease. Talk with your child's doctor if you think your child may be at risk.

Infantile hemangiomas are more common in the following:

• Girls.
• Whites.
• Premature babies.
• Twins, triplets, or other multiple births.
• Babies of mothers who are older at time of the pregnancy or who have problems with the placenta during pregnancy.

Other risk factors for infantile hemangiomas include the following:

• Having a family history of infantile hemangioma, usually in a mother, father, sister, or brother.
• Having certain syndromes.

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  PHACE syndrome: A syndrome in which the hemangioma spreads across a large area of the body (usually the head or face). Other health problems that affect the large blood vessels, heart, eyes, and/or brain may also occur.

  -

  LUMBAR/PELVIS/SACRAL syndrome: A syndrome in which the hemangioma spreads across a large area of the lower back. Other health problems that affect the urinary system, genitals, rectum, anus, brain, spinal cord, and nerve function may also occur.

Having more than one hemangioma or an airway or periorbital hemangioma increases the risk of having other health problems.

• Multiple hemangiomas: Having more than five hemangiomas on the skin is a sign that there may be hemangiomas in an organ. The liver is affected most often. Heart, muscle, and thyroid gland problems can also occur.
• Airway hemangiomas: Hemangiomas in the airway usually occur along with a large, beard-shaped area of hemangioma on the face (from the ears, around the mouth, lower chin, and front of neck). It is important that airway hemangiomas are treated before the child has trouble breathing.
• Periorbital hemangiomas: Hemangiomas around the eye may cause vision problems or blindness. It is important that children with a periorbital hemangioma are examined by an ophthalmologist.

Signs and Symptoms

Infantile hemangiomas may cause any of the following signs and symptoms. Check with your child’s doctor if your child has any of the following:

• Skin lesions: An area of spidery veins or lightened or discolored skin may appear before the hemangioma does. Hemangiomas occur as firm, warm, bright red to crimson lesions on the skin or may look like a bruise. Lesions that form ulcers are also painful. Later, as the hemangiomas go away, they begin fading in the center before flattening and losing color.
• Lesions below the skin: Lesions that grow under the skin in the fat may appear blue or purple. If the lesions are deep enough under the skin surface, they may not be seen.
• Lesions in an organ: There may be no signs that hemangiomas have formed on an organ.

Although most infantile hemangiomas are nothing to worry about, if your child develops any lumps or red or blue marks on the skin check with your child's doctor. He or she can refer the child to a specialist if needed.

Diagnostic Tests

A physical exam and history are usually all that are needed to diagnose infantile hemangiomas. If there is something about the tumor that looks unusual, a biopsy may be done. If the hemangioma is deeper inside the body with no change to the skin, or the lesions are spread across a large area of the body, an ultrasound may be done. See the General Information section for a description of these tests and procedures.

If the hemangiomas are part of a syndrome, more tests may be done, such as an echocardiogram, MRI, magnetic resonance angiogram, and eye exam.

Treatment

Most hemangiomas fade and shrink without treatment. If the hemangioma is large or causing other health problems, treatment may include the following:

• Propranolol or other beta-blocker therapy.
• Steroid therapy, before beta-blocker therapy is begun or when beta-blockers cannot be used.
• Pulsed dye laser surgery, for hemangiomas that have ulcers or have not completely gone away.
• Surgery (excision) for hemangiomas that have ulcers, cause vision problems, or have not completely gone away. Surgery may also be used for lesions on the face that do not respond to other treatment.
• Topical beta-blocker therapy for hemangiomas that are in one area of the skin.
• Combined therapy, such as propranolol and steroid therapy or propranolol and topical beta-blocker therapy.
• A clinical trial of beta-blocker therapy (nadolol and propranolol).
• A clinical trial of topical beta-blocker therapy (timolol).

Congenital Hemangioma

Congenital hemangioma is a benign vascular tumor that begins forming before birth and is fully formed when the baby is born. They're usually on the skin but can be in another organ. A congenital hemangioma may occur as a rash of purple spots and the skin around the spot may be lighter.

There are three types of congenital hemangiomas:

• Rapidly Involuting Congenital Hemangioma: These tumors go away on their own 12 to 15 months after birth. They can form ulcers, bleed, and cause temporary heart and blood clotting problems. The skin may look a little different even after the hemangiomas go away.
• Partial Involuting Congenital Hemangioma: These tumors do not go away completely.
• Non-Involuting Congenital Hemangioma: These tumors never go away on their own.

Diagnostic Tests

See the General Information section for a description of tests and procedures used to diagnose congenital hemangioma.

Treatment

Treatment of rapidly involuting congenital hemangioma and partial involuting congenital hemangioma may include the following:

• Observation only.

Treatment of non-involuting congenital hemangioma may include the following:

• Surgery to remove the tumor, depending on where it is and whether it is causing symptoms.

Benign Vascular Tumors of the Liver

Benign vascular tumors of the liver may be focal vascular lesions (a single lesion in one area of the liver), multiple liver lesions (multiple lesions in one area of the liver), or diffuse liver lesions (multiple lesions in more than one area of the liver).

The liver has many functions, including filtering blood and making proteins needed for blood clotting. Sometimes, blood that normally flows through the liver is blocked or slowed by the tumor. This sends blood directly to the heart without going through the liver and is called a liver shunt. This can cause heart failure and problems with blood clotting.

Focal Vascular Lesions

Focal vascular lesions are usually rapidly involuting congenital hemangiomas or non-involuting congenital hemangiomas.

Diagnostic Tests

See the General Information section for a description of tests and procedures used to diagnose focal vascular lesions of the liver.

Treatment

Treatment of focal vascular lesions of the liver depends on whether symptoms occur and may include the following:

• Observation.
• Drugs to treat symptoms, including heart failure and blood clotting problems.
• Embolization of the liver to treat symptoms.
• Surgery, for lesions that do not respond to other treatment.

Multiple and Diffuse Liver Lesions

Multifocal and diffuse lesions of the liver are usually infantile hemangiomas. Diffuse lesions of the liver can cause serious effects, including problems with the thyroid gland and heart. The liver can enlarge, press on other organs, and cause more symptoms.

Diagnostic Tests

See the General Information section for a description of tests and procedures used to diagnose multifocal or diffuse benign vascular lesions.

Treatment

Treatment of multifocal liver lesions may include the following:

• Observation for lesions that do not cause symptoms.
• Beta-blocker therapy (propranolol) for lesions that begin to grow.

Treatment of diffuse liver lesions may include the following:

• Beta-blocker therapy (propranolol).
• Chemotherapy.
• Steroid therapy.
• Total hepatectomy and liver transplant, when the lesions do not respond to drug therapy. This is done only when the lesions have spread widely in the liver and more than one organ has failed.

If a vascular lesion of the liver does not respond to standard treatments, a biopsy may be done to see if the tumor has become malignant.

Spindle Cell Hemangioma

Spindle cell hemangiomas contain cells called spindle cells. Under a microscope, spindle cells look long and slender.

Risk Factors

Anything that increases your risk of getting a disease is called a risk factor. Having a risk factor does not mean that you will get the disease; not having risk factors doesn’t mean that you will not get the disease. Talk with your child's doctor if you think your child may be at risk. Spindle cell hemangiomas are likely to occur in children with the following syndromes:

• Maffucci syndrome, which affects cartilage and skin.
• Klippel-Trenaunay syndrome, which affects blood vessels, soft tissues, and bones.

Signs

Spindle cell hemangiomas appear on or under the skin. They are painful red-brown or bluish lesions that usually appear on the arms or legs. They can begin as one lesion and develop into more lesions over years.

Diagnostic Tests

See the General Information section for a description of tests and procedures used to diagnose spindle cell hemangioma.

Treatment

There is no standard treatment for spindle cell hemangiomas. Treatment may include the following:

• Surgery to remove the tumor.

Spindle cell hemangiomas may come back after surgery.

Epithelioid Hemangioma

Epithelioid hemangiomas usually form on or in the skin, especially the head, but can occur in other areas, such as bone.

Signs and Symptoms

Epithelioid hemangiomas are sometimes caused by injury. On the skin, they may appear as firm pink to red bumps and may be itchy. Epithelioid hemangioma of the bone may cause swelling, pain, and weakened bone in the affected area.

Diagnostic Tests

See the General Information section for a description of tests and procedures used to diagnose epithelioid hemangioma.

Treatment

There is no standard treatment for epithelioid hemangiomas. Treatment may include the following:

• Surgery (curettage or resection).
• Sclerotherapy.
• Radiation therapy in rare cases.

Epithelioid hemangiomas often come back after treatment.

Pyogenic Granuloma

Pyogenic granuloma is also called lobular capillary hemangioma. It is most common in older children and young adults but may occur at any age.

The lesions are sometimes caused by injury or from the use of certain medicines, including birth control pills and retinoids. They may also form for no known reason inside capillaries (the smallest blood vessels), arteries, veins, or other places on the body. Usually there is only one lesion, but sometimes multiple lesions occur in the same area or the lesions may spread to other areas of the body.

Signs

Pyogenic granulomas are raised, bright red lesions that may be small or large and smooth or bumpy. They grow quickly over weeks to months and may bleed a lot.

Diagnostic Tests

See the General Information section for a description of tests and procedures used to diagnose pyogenic granuloma.

Treatment

Some pyogenic granulomas go away without treatment. Other pyogenic granulomas need treatment that may include the following:

• Surgery (excision or curettage) to remove the lesion.
• Photocoagulation.

Pyogenic granulomas often come back after treatment.

Angiofibroma

Angiofibromas are rare. They are benign skin lesions that usually occur with a condition called tuberous sclerosis (an inherited disorder that causes skin lesions, seizures, and mental disabilities).

Signs

Angiofibromas appear as red bumps on the face.

Diagnostic Tests

See the General Information section for a description of tests and procedures used to diagnose angiofibroma.

Treatment

Treatment of angiofibromas may include the following:

• Surgery (excision) to remove the tumor.
• Laser therapy.
• Targeted therapy (sirolimus).

Juvenile Nasopharyngeal Angiofibroma

Juvenile nasopharyngeal angiofibromas are benign tumors but they can grow into nearby tissue. They begin in the nasal cavity and may spread to the nasopharynx, the paranasal sinuses, the bone around the eyes, and sometimes to the brain.

Diagnostic Tests

See the General Information section for a description of tests and procedures used to diagnose juvenile nasopharyngeal angiofibroma.

Treatment

Treatment of juvenile nasopharyngeal angiofibromas may include the following:

• Surgery (excision) to remove the tumor.
• Radiation therapy.
• Chemotherapy.
• Immunotherapy (interferon).
• Targeted therapy (sirolimus).

Kaposiform Hemangioendothelioma and Tufted Angioma

Kaposiform hemangioendotheliomas and tufted angiomas are blood vessel tumors that occur in infants or young children. These tumors can cause Kasabach-Merritt phenomenon, a condition in which the blood is not able to clot and serious bleeding may occur. In Kasabach-Merritt phenomenon, the tumor traps and destroys platelets (blood-clotting cells). Then there aren't enough platelets in the blood when needed to stop bleeding. This type of vascular tumor is not related to Kaposi sarcoma.

Signs and Symptoms

Kaposiform hemangioendotheliomas and tufted angiomas usually occur on the skin of the arms and legs, but may also form in deeper tissues, such as muscle or bone, or in the chest or abdomen.

Signs and symptoms may include the following:

• Firm, painful areas of skin that look bruised.
• Purple or brownish-red areas of skin.
• Easy bruising.
• Bleeding more than the usual amount from mucous membranes, wounds, and other tissues.

Patients who have kaposiform hemangioendothelioma and tufted angioma may have anemia (weakness, feeling tired, or looking pale).

Diagnostic Tests

See the General Information section for a description of tests and procedures used to diagnose kaposiform hemangioendothelioma.

If a physical exam and MRI clearly show the tumor is a kaposiform hemangioendothelioma or a tufted angioma, a biopsy may not be needed. A biopsy is not always done because serious bleeding can occur.

Treatment

Treatment of kaposiform hemangioendotheliomas and tufted angiomas depends on the child's symptoms. Infection, delay in treatment, and surgery can cause bleeding that is life-threatening. Kaposiform hemangioendotheliomas and tufted angiomas are best treated by a vascular anomaly specialist.

Treatment and supportive care to manage bleeding may include the following:

• Steroid therapy which may be followed by chemotherapy.
• Non-steroidal anti-inflammatory drugs (NSAIDs), such as aspirin.
• Immunotherapy (interferon).
• Antifibrinolytic therapy to improve blood clotting.
• Chemotherapy with one or more anticancer drugs.
• Beta-blocker therapy (propranolol).
• Surgery (excision) to remove the tumor, with or without embolization.
• Targeted therapy (sirolimus), with or without steroid therapy.
• A clinical trial of chemotherapy or targeted therapy (sirolimus).

Even with treatment, these tumors do not fully go away and can come back. Pain and inflammation may get worse with age, often around the time of puberty. Long-term effects include chronic pain, heart failure, bone problems, and lymphedema (the build up of lymph fluid in tissues).

Pseudomyogenic Hemangioendothelioma

Pseudomyogenic hemangioendothelioma can occur in children, but is most common in men between 20 and 50 years of age. These tumors are rare, and usually occur on or under the skin, or in bone. They may spread to nearby tissue, but usually do not spread to other parts of the body. In most cases, there are multiple tumors.

Signs and Symptoms

Pseudomyogenic hemangioendotheliomas may appear as a lump in soft tissue or may cause pain in the affected area.

Diagnostic Tests

See the General Information section for a description of tests and procedures used to diagnose pseudomyogenic hemangioendothelioma.

Treatment

Treatment of pseudomyogenic hemangioendotheliomas may include the following:

• Surgery to remove the tumor when possible. Amputation may be needed when there are multiple tumors in the bone.
• Chemotherapy.
• Targeted therapy (mTOR inhibitors).

Because pseudomyogenic hemangioendothelioma is so rare in children, treatment options are based on clinical trials in adults.

Retiform Hemangioendothelioma

Retiform hemangioendotheliomas are slow growing, flat tumors that occur in young adults and sometimes children. These tumors usually occur on or under the skin of the arms, legs, and trunk. These tumors usually do not spread to other parts of the body.

Diagnostic Tests

See the General Information section for a description of tests and procedures used to diagnose retiform hemangioendothelioma.

Treatment

Treatment of retiform hemangioendotheliomas may include the following:

• Surgery (excision) to remove the tumor. Follow up will include monitoring to see if the tumor comes back.
• Radiation therapy and chemotherapy when surgery cannot be done or when the tumor has come back.

Retiform hemangioendothelioma may come back after treatment.

Papillary Intralymphatic Angioendothelioma

Papillary intralymphatic angioendotheliomas are also called Dabska tumors. These tumors form in or under the skin anywhere on the body. Lymph nodes are sometimes affected.

Signs

Papillary intralymphatic angioendotheliomas may appear as firm, raised, purplish bumps, which may be small or large.

Diagnostic Tests

See the General Information section for a description of tests and procedures used to diagnose papillary intralymphatic angioendothelioma.

Treatment

Treatment of papillary intralymphatic angioendotheliomas may include the following:

• Surgery (excision) to remove the tumor.

Composite Hemangioendothelioma

Composite hemangioendotheliomas have features of both benign and malignant vascular tumors. These tumors usually occur on or under the skin on the arms or legs. They may also occur on the head, neck, or chest. Composite hemangioendotheliomas are not likely to metastasize (spread) but they may come back in the same place. When the tumors metastasize, they usually spread to nearby lymph nodes.

Diagnostic Tests

See the General Information section for a description of tests and procedures used to diagnose composite hemangioendothelioma and find out whether the tumor has spread.

Treatment

Treatment of composite hemangioendotheliomas may include the following:

• Surgery to remove the tumor.
• Radiation therapy and chemotherapy for tumors that have spread.

Kaposi Sarcoma

Kaposi sarcoma is a cancer that causes lesions to grow in the skin; the mucous membranes lining the mouth, nose, and throat; lymph nodes; or other organs. It is caused by the Kaposi sarcoma herpes virus (KSHV). In the United States, it occurs most often in children who have a weak immune system caused by rare immune system disorders, HIV infection, or drugs used in organ transplants.

Signs

Signs in children may include the following:

• Lesions in the skin, mouth, or throat. Skin lesions are red, purple, or brown and change from flat, to raised, to scaly areas called plaques, to nodules.
• Swollen lymph nodes.

Diagnostic Tests

See the General Information section for a description of tests and procedures used to diagnose Kaposi sarcoma.

Treatment

Treatment of Kaposi sarcoma may include the following:

• Chemotherapy.
• Immunotherapy (interferon).
• Radiation therapy.

Because Kaposi sarcoma is so rare in children, some treatment options are based on clinical trials in adults. See the PDQ summary on Kaposi Sarcoma Treatment for information about Kaposi sarcoma in adults.

Epithelioid Hemangioendothelioma

Epithelioid hemangioendotheliomas can occur in children, but are most common in adults between 30 and 50 years of age. They usually occur in the liver, lung, or in bone. They may be fast growing or slow growing. In about a third of cases, the tumor spreads to other parts of the body very quickly.

Signs and Symptoms

Signs and symptoms depend on where the tumor is:

• On the skin, the tumors can be raised and rounded or flat, red-brown patches that feel warm.
• In the lung, there may be no early symptoms. Signs and symptoms that may occur include:

  -

  Chest pain.

  -

  Spitting up blood.

  -

  Anemia (weakness, feeling tired, or looking pale).

  -

  Trouble breathing (from scarred lung tissue).

• In bone, the tumors can cause breaks.

Tumors that occur in the liver or soft tissue may also cause signs and symptoms.

Diagnostic Tests

Epithelioid hemangioendotheliomas in the liver are found with CT scans and MRI scans. See the General Information section for a description of these tests and procedures used to diagnose epithelioid hemangioendothelioma and find out whether the tumor has spread. X-rays may also be done.

Treatment

Treatment of slow-growing epithelioid hemangioendotheliomas includes the following:

• Observation.

Treatment of fast-growing epithelioid hemangioendotheliomas may include the following:

• Surgery to remove the tumor when possible.
• Immunotherapy (interferon) and targeted therapy (thalidomide, sorafenib, pazopanib, sirolimus) for tumors that are likely to spread.
• Chemotherapy.
• Total hepatectomy and liver transplant when the tumor is in the liver.
• A clinical trial of targeted therapy (trametinib).
• A clinical trial of chemotherapy and targeted therapy (pazopanib).

Angiosarcoma of the Soft Tissue

Angiosarcomas are fast-growing tumors that form in blood vessels or lymph vessels in any part of the body, usually in soft tissue. Most angiosarcomas are in or near the skin. Those in deeper soft tissue can form in the liver, spleen, and lung.

These tumors are very rare in children. Children sometimes have more than one tumor in the skin and/or liver.

Risk Factors

Anything that increases your risk of getting a disease is called a risk factor. Having a risk factor does not mean that you will get the disease; not having risk factors doesn’t mean that you will not get the disease. Talk with your child's doctor if you think your child may be at risk. Risk factors for angiosarcomas include the following:

• Being exposed to radiation.
• Chronic (long-term) lymphedema, a condition in which extra lymph fluid builds up in tissues and causes swelling.
• Having a benign vascular tumor. A benign tumor, such as a hemangioma, may become an angiosarcoma but this is rare.

Signs

Signs of angiosarcoma depend on where the tumor is and may include the following:

• Red patches on the skin that bleed easily.
• Purple tumors.

Diagnostic Tests

See the General Information section for a description of tests and procedures used to diagnose angiosarcoma and find out whether the tumor has spread.

Treatment

Treatment of angiosarcoma may include the following:

• Surgery to completely remove the tumor.
• A combination of surgery, chemotherapy, and radiation therapy for angiosarcomas that have spread.
• A clinical trial of radiation therapy, surgery with or without chemotherapy, and targeted therapy (pazopanib).
• A clinical trial of chemotherapy with or without targeted therapy (pazopanib).

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This PDQ cancer information summary has current information about the treatment of childhood vascular tumors. It is meant to inform and help patients, families, and caregivers. It does not give formal guidelines or recommendations for making decisions about health care.

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Editorial Boards write the PDQ cancer information summaries and keep them up to date. These Boards are made up of experts in cancer treatment and other specialties related to cancer. The summaries are reviewed regularly and changes are made when there is new information. The date on each summary ("Date Last Modified") is the date of the most recent change.

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PDQ® Pediatric Treatment Editorial Board. PDQ Childhood Vascular Tumors Treatment. Bethesda, MD: National Cancer Institute. Updated <MM/DD/YYYY>. Available at: https://www.cancer.gov/types/soft-tissue-sarcoma/patient/child-vascular-tumors-treatment-pdq. Accessed <MM/DD/YYYY>. [PMID: 27253005]

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The information in these summaries should not be used to make decisions about insurance reimbursement. More information on insurance coverage is available on Cancer.gov on the Managing Cancer Care page.

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More information about contacting us or receiving help with the Cancer.gov website can be found on our Contact Us for Help page. Questions can also be submitted to Cancer.gov through the website’s E-mail Us.