Pilomatrixoma
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What is pilomatrixoma? | |
What causes pilomatrixoma? | |
| Pilomatrixomas develop from an abnormal formation of cells that are similar to hair cells, which become hardened or calcified. The calcified cells form a mass beneath the skin. | |
| Other members of a child's family may also have pilomatrixoma, suggesting a genetic component. | |
What are the symptoms of pilomatrixoma? | |
| The following are the most common symptoms of pilomatrixoma. However, each child may experience symptoms differently. Symptoms may include a small, hard mass beneath the skin of the face, head, neck, or arms. The mass is usually less than 3 centimeters in diameter and the skin covering the mass appears normal, or may feel firm or hardened. Usually, the mass is painless, unless it becomes infected. | |
| The symptoms of pilomatrixoma may resemble other neck masses or medical problems. Always consult your child's physician for a diagnosis. | |
How is pilomatrixoma diagnosed? | |
| Generally, pilomatrixoma is diagnosed by physical examination. In addition to a complete medical history and physical examination, diagnostic procedures for pilomatrixoma may include a biopsy - a procedure in which tissue samples are removed (with a needle or during surgery) from the body for examination under a microscope; to determine if cancer or other abnormal cells are present. | |
Treatment of pilomatrixoma: | |
| Specific treatment of pilomatrixoma will be determined by your child's physician based on: | |
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| Treatment may include surgery to remove the mass and some of the surrounding tissue. Pilomatrixomas cysts usually do not regrow. | |
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