Extraskeletal chondroma

From WikiMD's Food, Medicine & Wellness Encyclopedia

Extraskeletal Chondroma is a rare, benign tumor that develops in the soft tissues of the hands and feet. It is composed of cartilage but is not attached to the bone or periosteum.

Symptoms[edit | edit source]

The most common symptom of an extraskeletal chondroma is a slow-growing, painless mass. The mass is typically less than 3 cm in diameter. Pain or tenderness may occur if the tumor compresses nearby nerves.

Causes[edit | edit source]

The exact cause of extraskeletal chondroma is unknown. It is not associated with any known risk factors or genetic mutations.

Diagnosis[edit | edit source]

Diagnosis of extraskeletal chondroma is typically made through a combination of physical examination, imaging studies, and biopsy. Imaging studies such as MRI or CT scan can help to determine the size and location 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[edit | edit source]

Treatment for extraskeletal chondroma typically involves surgical removal of the tumor. In some cases, radiation therapy may be used if the tumor cannot be completely removed.

Prognosis[edit | edit source]

The prognosis for individuals with extraskeletal chondroma is generally good. The tumor is benign and does not spread to other parts of the body. However, there is a risk of local recurrence if the tumor is not completely removed.

See also[edit | edit source]

Extraskeletal chondroma Resources
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