Epithelioid sarcoma

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Epithelioid sarcoma
Micrograph of epithelioid sarcoma
Synonyms N/A
Pronounce N/A
Specialty N/A
Symptoms Nodule, ulceration, pain
Complications Metastasis
Onset Typically in young adults
Duration Chronic
Types Distal, proximal
Causes Unknown
Risks Male gender, young adult
Diagnosis Biopsy, immunohistochemistry
Differential diagnosis Synovial sarcoma, granuloma, epidermoid cyst
Prevention None known
Treatment Surgery, radiation therapy, chemotherapy
Medication Doxorubicin, ifosfamide
Prognosis Variable, depends on stage and location
Frequency Rare
Deaths N/A


Epithelioid sarcoma is a rare type of sarcoma that typically arises in the soft tissue of the extremities, often in the hands or feet. It is characterized by the presence of epithelioid cells, which resemble the epithelial cells that line the body's cavities and surfaces.

Symptoms[edit]

The most common symptom of epithelioid sarcoma is a slow-growing lump or swelling. This may be accompanied by pain or discomfort. In some cases, the disease may cause skin ulcers or other changes in the skin.

Causes[edit]

The exact cause of epithelioid sarcoma is unknown. However, it is thought to arise from changes in the DNA of cells, which cause them to grow and divide uncontrollably.

Diagnosis[edit]

Diagnosis of epithelioid sarcoma typically involves a combination of physical examination, imaging tests such as MRI or CT scan, and biopsy. The biopsy sample is examined under a microscope to look for the characteristic epithelioid cells.

Treatment[edit]

Treatment for epithelioid sarcoma usually involves surgery to remove the tumor. This may be followed by radiation therapy or chemotherapy to kill any remaining cancer cells. In some cases, targeted therapies or immunotherapies may be used.

Prognosis[edit]

The prognosis for epithelioid sarcoma varies depending on the size and location of the tumor, the patient's overall health, and the extent to which the disease has spread at the time of diagnosis.

Images[edit]

See also[edit]

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