Hemangioendothelioma

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(Redirected from Retiform hemangioendothelioma)

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Hemangioendothelioma
Kaposiform hemangioendothelioma
Synonyms
Pronounce N/A
Specialty N/A
Symptoms Pain, swelling, skin lesions
Complications Metastasis, Kasabach-Merritt syndrome
Onset Varies by subtype
Duration Chronic
Types Epithelioid hemangioendothelioma, Kaposiform hemangioendothelioma, Retiform hemangioendothelioma
Causes Unknown
Risks
Diagnosis Biopsy, imaging studies
Differential diagnosis Angiosarcoma, Hemangioma
Prevention N/A
Treatment Surgery, chemotherapy, radiation therapy
Medication
Prognosis Varies by subtype and stage
Frequency Rare
Deaths N/A


Dabska tumor histology
Dabska tumor histology 2
Hemangioendothelioma

Hemangioendothelioma is a rare type of vascular tumor that occurs in the blood vessels. It is a borderline neoplasm, meaning it is neither entirely benign nor malignant. Hemangioendotheliomas can occur anywhere in the body, but are most commonly found in the liver, lung, and bone.

Symptoms

The symptoms of hemangioendothelioma can vary greatly depending on the location of the tumor. Some common symptoms include pain, swelling, and a noticeable lump or mass. If the tumor is in the liver, symptoms may also include jaundice, abdominal pain, and weight loss.

Diagnosis

Diagnosis of hemangioendothelioma typically involves a combination of imaging studies, biopsy, and pathological examination. Imaging studies such as CT or MRI can help to identify the location and size of the tumor. A biopsy, in which a small sample of the tumor is removed for examination under a microscope, can confirm the diagnosis.

Treatment

Treatment for hemangioendothelioma depends on the size and location of the tumor, as well as the patient's overall health. Options may include surgery, radiation therapy, chemotherapy, or a combination of these. In some cases, if the tumor is small and not causing any symptoms, doctors may choose to monitor it closely rather than treat it immediately.

Prognosis

The prognosis for hemangioendothelioma varies widely depending on the location and size of the tumor, as well as the patient's overall health. Some tumors are slow-growing and may not cause any symptoms for many years, while others can be more aggressive and spread to other parts of the body.

See also

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Contributors: Prab R. Tumpati, MD