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Vitiligo

Also called: Common Vitiligo, Vitiligo Vulgaris

- Summary
- About vitiligo
- Types and differences
- Risk factors and causes
- Signs and symptoms
- Diagnosis methods
- Treatment and prevention
- Questions for your doctor

Reviewed By:
Kimberly Bazar, M.D., AAD
Mary Ellen Luchetti, M.D., AAD

Diagnosis methods for vitiligo

The diagnosis of vitiligo involves a physician taking a medical history and performing a physical examination. Blood tests or other tests are not normally required. In the evaluation of a patient’s medical history, a physician will look for certain information, including:

  • Whether there is a family history of vitiligo

  • Any rash, sunburn or other trauma of the skin two to three months prior to depigmentation

  • Any recent stress or physical illness

  • Presence of gray hair before the age of 35

  • Patient or family history of autoimmune diseases (e.g., thyroid disorder)

  • Any increased sensitivity to the sun

Physical examination includes examination under visible and ultraviolet light. Examination under visible light generally reveals white skin macules (patches), but it may be difficult to distinguish between vitiligo and other causes for light patches of skin. Wood’s lamp examination uses ultraviolet A light to detect truly depigmented areas. The white skin of vitiligo has a characteristic yellow-green or blue fluorescence under this form of examination.

Although not usually necessary, a physician may take a skin biopsy from a depigmented macule to rule out other causes of pigment loss. When a patient has vitiligo, there will be no pigment present within the melanocytes (pigment producing cells) when the sample is stained. Blood tests may be performed to check thyroid function and to look for antibodies. A physician may refer a patient to an ophthalmologist (eye physician) for an examination to check for inflammation of certain internal eye structures (uveitis).

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Review Date: 01-18-2007
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