II. Pathophysiology
- Immune-mediated Melanocyte destruction
- Family History present in up to 30% of patients
III. Epidemiology
- Affects 0.5 to 2% of the population
- Onset peaks between age 10-30 years (50% occur by age 20 years)
- Occurs equally in men and women
IV. Types
- Localized Vitiligo or Segmental Vitiligo (seen more in children)- Stable involvement, stops progressing at a young age
- Affects a small body area or unilateral single Dermatome or extremity involved
 
- 
                          Generalized Vitiligo or Nonsegmental Vitiligo- Affects >10% of body surface area, typically bilateral and symmetric
- Progresses over time
 
- Acral or Acrofacial Vitiligo- Lip-Tip pattern: Face and distal extremities
 
V. History
- Triggers- Recent stress, illness or local Trauma
 
VI. Signs
- Sharply demarcated, white, unpigmented or hypopigmented Macules 0.5 to 5 cm in size- May coalesce together
 
- More noticeable on dark skin
- Distribution- Face and neck
- Dorsal hands
- Genitalia
- Intertriginous folds and axillae
- Periocular, periumbilical, and perianal areas
 
VII. Associated Conditions
VIII. Management
- Approach- Head an neck lesions respond better to treatment than extremity and genital lesions
- Combination therapy is more effective than monotherapy, but often refractory to any treatment
- Recurrence is common (40% of cases)
 
- Localized Vitiligo Management- Topical Corticosteroids, high potency, class II-III (safest and most effective localized treatment)- Safest and most effect
- Betamethasone 0.1% ointment
- Fluocinonide 0.05% ointment
 
- Topical Calcineurin Inhibitors
- Surgical grafting- May be used for localized, stable lesions
- Split thickness graft
- Suction Blister epidermal grafting
 
 
- Topical Corticosteroids, high potency, class II-III (safest and most effective localized treatment)
- 
                          Generalized or refractory Vitiligo Management (by Dermatology)- Narrowband Ultraviolet B or UVB (safest and most effective generalized treatment)
- Phototherapy with Psoralens or PUVA
- Systemic Corticosteroids
- Depigmentation (indicated for >40-50% of BSA involvement)- Permanent depigmentation with Monobenzone 20% cream (no longer available in U.S.)
- Cryotherapy and laser therapy has been used as an alternative
- Requires 6-18 months for full treatment
 
 
- Cosmetic- Concealers (e.g. Dermablend, Covermark)
- Topical dyes
- Sunless self-tanning products (skin types 2-3)
 
IX. Prevention
- Sun protection is critical (clothing, Sunscreen)
