Epithelioid cell histiocytoma

From WikiMD's Wellness Encyclopedia

Epithelioid cell histiocytoma is a rare, benign skin tumor that is characterized by the presence of epithelioid cells. These cells, which are typically found in the epidermis, have a unique appearance that is similar to that of epithelial cells. However, unlike epithelial cells, epithelioid cells are part of the immune system and play a role in the body's response to infection and inflammation.

History[edit | edit source]

Epithelioid cell histiocytoma was first described in the medical literature in the late 20th century. Since then, it has been the subject of numerous case studies and research articles, which have helped to further our understanding of this rare condition.

Symptoms and Diagnosis[edit | edit source]

Epithelioid cell histiocytoma typically presents as a solitary, red or brown nodule on the skin. It is most commonly found on the extremities, but can occur anywhere on the body. The tumor is usually painless, but may be associated with mild discomfort or itching.

Diagnosis of epithelioid cell histiocytoma is typically made through a biopsy of the affected skin. Under the microscope, the tumor is characterized by the presence of large, round cells with abundant cytoplasm and centrally located nuclei. These cells, known as epithelioid histiocytes, are often surrounded by a dense inflammatory infiltrate.

Treatment and Prognosis[edit | edit source]

Treatment for epithelioid cell histiocytoma typically involves surgical removal of the tumor. This is usually curative, as the tumor is benign and does not spread to other parts of the body. However, recurrence after surgery is possible, so regular follow-up visits with a dermatologist or oncologist are recommended.

The prognosis for individuals with epithelioid cell histiocytoma is generally excellent. With appropriate treatment, most individuals experience complete recovery and can expect to live a normal, healthy life.

See Also[edit | edit source]

References[edit | edit source]


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Contributors: Prab R. Tumpati, MD