Epithelioid Hemangioendothelioma (2024)

What is epithelioid hemangioendothelioma?

Epithelioid hemangioendotheliomais a rare type of vascular tumor that affects the epithelial cells, which line the inside of blood vessels. Epithelioid hemangioendothelioma tumors most commonly affect the soft tissues, liver, lungs and bones.

These tumors are malignant (cancerous). But they are slow-growing and do not usually spread (metastasize) as quickly as other cancers. Because they are so rare, they can go undetected for a long time before being diagnosed. This gives the tumors time to spread to surrounding tissues.

Epithelioid hemangioendothelioma tumors affect each person differently. Some people can live with these slow-growing tumors for years with only minor disruption to daily life. Sometimes the tumors even go away on their own. Less commonly, the tumors grow and spread quickly.

The cause of epithelioid hemangioendothelioma is not known.

How common is epithelioid hemangioendothelioma?

Vascular tumors are uncommon. They represent about 2% of soft tissue tumors in children and teens.

What are the signs and symptoms of epithelioid hemangioendothelioma?

Epithelioid hemangioendothelioma can appear anywhere in the body. Its symptoms often depend on the tumor’s location. The most common symptoms include the following:

  • Weight loss
  • Pain and swelling in the tumor area, such as pain in the abdomen
  • Mass in the tumor area
  • Skin nodules that may be red or blue
  • Enlarged organ affected by the tumor, such as the liver or spleen
  • Problems moving or walking, such as if the tumor occurs in the spine

How is epithelioid hemangioendothelioma treated?

Epithelioid hemangioendothelioma treatment varies based on tumor location and grade (how severe it is).

A common treatment is surgery. The surgeon will remove as much surrounding tissue as needed to provide a margin of healthy tissue.

Doctors may also use radiation, chemotherapy or targeted therapies to treat epithelioid hemangioendothelioma.

A person with epithelioid hemangioendothelioma in the liver may receive a liver transplant.

In some cases, if the tumor is spreading slowly, your child’s doctor may take a wait-and-see approach to monitor tumor growth rather than subject your child to the risks and side effects of treatment.

What are the survival rates for epithelioid hemangioendothelioma?

Survival rates for epithelioid hemangioendothelioma are not well known and vary depending on the tumor location and type of treatment:

  • Liver epithelioid hemangioendothelioma: A 2006 study of 434 people with this type of epithelioid hemangioendothelioma found five-year survival rates of 55% in people with liver transplants and 30% in people who had chemotherapy or radiation. Two large-scale studies since then have shown even higher rates of survival for people who received liver transplants.
  • One estimate places the mortality rate for soft-tissue epithelioid hemangioendotheliomas at 13% to 18%.

Why choose St. Jude for your child’s epithelioid hemangioendothelioma treatment?

  • St. Jude is the only National Cancer Institute-designated Comprehensive Cancer Center devoted solely to children.
  • St. Jude has created more clinical trials for cancer than any other children’s hospital in the United States.
  • The nurse-to-patient ratio at St. Jude is unmatched— averaging 1:3 in hematology and oncology and 1:1 in the Intensive Care Unit.
  • Your child will have access to a close-knit team of specialists that includes: surgeons; doctors and nurses who treat this cancer; doctors who specialize in radiation therapy, in hormones (endocrinologists), and in diagnosis (pathologists); experts in diagnostic imaging and nuclear medicine; dietitians; speech therapists; rehabilitation specialists (physical therapists, occupational therapists); child life specialists; psychologists; Quality of Life team members; experts who help manage and minimize the long-term or late effects of treatment; researchers; scientists; and many others.
  • The medical team works closely with laboratory researchers to bring new treatments from the laboratory to the clinic.

Keywords:

Primary: epithelioid hemangioendothelioma

Secondary: EHE, HEHE, vascular tumor, vascular cancer, hepatic epithelioid hemangioendothelioma

Epithelioid Hemangioendothelioma (2024)

FAQs

Epithelioid Hemangioendothelioma? ›

What is epithelioid hemangioendothelioma? Epithelioid hemangioendothelioma, or EHE, is a rare cancer that grows from the cells that make up the blood vessels. This cancer can occur anywhere in the body with the most common sites being the liver, lungs, and bone.

How long can you live with epithelioid hemangioendothelioma? ›

Epithelioid hemangioendothelioma tumors affect each person differently. Some people can live with these slow-growing tumors for years with only minor disruption to daily life. Sometimes the tumors even go away on their own. Less commonly, the tumors grow and spread quickly.

Is epithelioid hemangioendothelioma a cancer? ›

Epithelioid Hemangioendothelioma (EHE) is a rare cancer that belongs to the group of cancers called sarcomas. EHE is a vascular sarcoma. This means it originates in the cells that line the inside of blood vessels.

Is there a cure for epithelioid hemangioendothelioma? ›

Sometimes, these tumors shrink without treatment. In other instances, they grow slowly over many years. If your cancer worsens, your provider may recommend a different approach. Surgery: Surgery is the most common treatment for cases of EHE involving a single tumor.

What is the survival rate for hemangioendothelioma? ›

The overall 1-, 3-, and 5-year survival rates were 70.8% (95%CI = 48.4–84.9%), 61.2% (95%CI = 38.5–77.7%), and 55.6% (95%CI = 32.8–73.5%), respectively. The age-adjusted incidence rate of epithelioid hemangioendothelioma from 1975 to 2019.

What are the symptoms of epithelioid? ›

Epithelioid Sarcoma Symptoms and Signs
  • One or more lumps that can continue to grow.
  • Open skin wound above the lump.
  • Pain if the tumor forms near a joint or pushes on muscles or nerves.
  • Swelling.

What is the death rate of epithelioid sarcoma? ›

Five year survival and ten year survival rate for patients with epithelioid sarcoma are approximately 50-70% and 42-55% respectively.

How many people are diagnosed with epithelioid hemangioendothelioma? ›

How common is epithelioid hemangioendothelioma? EHE is very rare, with only one in every one million people diagnosed with this cancer worldwide.

What is Stage 4 epithelioid hemangioendothelioma sarcoma? ›

Stage IV: the cancer has spread to other tissues and organs in the body. This is also known as advanced or metastatic cancer.

What is the cause of hemangioendothelioma? ›

Hemangioendotheliomas are caused by abnormal growth of blood vessel cells, although the exact underlying cause for the abnormal growth is unknown. They can also develop in an organ, such as the liver or lung. They usually grow slowly and can sometimes spread to other tissues in the body (metastasize).

What is the difference between angiosarcoma and EHE? ›

Epithelioid hemangioendothelioma (EHE) is a low-to-intermediate-grade vascular tumor that occurs in many organs, and epithelioid angiosarcoma (EA) is a subtype of angiosarcoma that is associated with high-grade malignancy. These two types of tumors have different forms of biological behavior.

Is EHE a sarcoma? ›

This is a vascular tumor that may occur anywhere throughout the body. This tumor behaves on a spectrum as either a benign tumor or an aggressive sarcoma. The EHE tumor and its management depend on the location of the lesion and accessibility for surgical excision.

What is the prognosis for epithelioid MPNST? ›

The main clinical manifestations are pain and numbness; however, they are not specific symptoms, and MPNSTs are difficult to distinguish from other nerve lesions [5,7,8,9,10]. MPNST is still difficult to diagnose and treat, and the overall prognosis is poor. Although MPNST is a rare disease, the mortality rate is high.

How fast does epithelioid sarcoma grow? ›

Epithelioid sarcoma is slow growing. A person can have this type of cancer for months (or even years) before noticing any symptoms. Another name for this condition is epithelial sarcoma. There are two types: distal and proximal.

What are the stages of epithelioid sarcoma? ›

Staging of epithelioid sarcoma is based on the size of the tumor and whether it has spread to lymph nodes or distant sites in the body. If the tumor has not spread, it is considered to be localized. Metastatic epithelioid sarcoma means the tumor has spread past nearby tissues to lungs or other organs.

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