Epithelioid hemangioendothelioma
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| Epithelioid hemangioendothelioma | |
|---|---|
| File:Epithelioid hemangioendothelioma.jpg | |
| Synonyms | EHE |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Pain, swelling, fatigue |
| Complications | Metastasis, organ failure |
| Onset | Any age, often in young adults |
| Duration | Chronic |
| Types | Soft tissue, liver, lung |
| Causes | Unknown |
| Risks | Genetic mutations, environmental factors |
| Diagnosis | Biopsy, imaging studies |
| Differential diagnosis | Angiosarcoma, hemangioma, sarcoma |
| Prevention | N/A |
| Treatment | Surgery, chemotherapy, radiation therapy |
| Medication | N/A |
| Prognosis | Variable, depends on stage and location |
| Frequency | Rare |
| Deaths | N/A |
Epithelioid hemangioendothelioma (EHE) is a rare form of cancer that originates from the cells lining the blood vessels, known as endothelial cells. This type of cancer can occur in various parts of the body, including the liver, lung, bone, and soft tissue.
Symptoms[edit]
The symptoms of EHE can vary depending on the location of the tumor. Common symptoms may include pain, swelling, and fatigue. In some cases, EHE may not cause any symptoms and is discovered incidentally during imaging tests for other conditions.
Causes[edit]
The exact cause of EHE is unknown. However, it is believed to be associated with certain genetic mutations.
Diagnosis[edit]
Diagnosis of EHE typically involves a combination of medical history, physical examination, imaging tests such as CT scan or MRI, and biopsy of the tumor.
Treatment[edit]
Treatment options for EHE depend on the size and location of the tumor, as well as the patient's overall health. Treatment may include surgery, radiation therapy, chemotherapy, or targeted therapy.
Prognosis[edit]
The prognosis for EHE varies widely and depends on several factors, including the size and location of the tumor, the patient's overall health, and the response to treatment.
See also[edit]
References[edit]
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