Vitiligo: Causes, Symptoms, and Treatment Options
Vitiligo is an autoimmune disorder where melanocytes are destroyed, causing depigmented white patches on skin and mucosa.
Key Features
- Distribution: Generalized (symmetrical), segmental (dermatomal), focal, acrofacial, universal.
- Onset: Often before age 30; 50% childhood.
- Associations: Thyroid autoimmunity (Hashimoto's, Graves'), alopecia areata, type 1 diabetes, pernicious anemia.
- Koebner phenomenon: New lesions at trauma sites.
Diagnosis
- Clinical: Chalk-white macules, sharp margins, Wood's lamp enhancement.
- Biopsy rarely needed; shows absent melanocytes.
- Screen for autoimmune comorbidities (TSH, TPO Ab, ANA, CBC, glucose).
Treatment (Goal: Stabilize + Repigment)
- Topical: Corticosteroids (mid-potency), calcineurin inhibitors (tacrolimus, pimecrolimus) — face/folds.
- Phototherapy: Narrowband UVB (NB-UVB) 2–3×/week — gold standard for widespread disease. Excimer laser for localized.
- Systemic: Low-dose oral steroids (minipulse) for rapid stabilization; JAK inhibitors (ruxolitinib cream FDA-approved 2022; oral in trials).
- Surgical (stable disease >1 yr): Suction blister grafting, melanocyte-keratinocyte transplant (MKTP).
- Camouflage: Dermablend, Microskin, tattooing (micropigmentation).
Psychosocial Support
Vitiligo significantly impacts quality of life. Counseling, support groups (Vitiligo Support International), and advocacy reduce stigma.
Early treatment yields better repigmentation. See a dermatologist experienced in vitiligo.
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