Treatment of Hypopigmentation
For post-inflammatory hypopigmentation on the face, start with topical tacrolimus or pimecrolimus applied twice daily for 8-12 weeks, which achieves approximately 50% repigmentation and has a superior safety profile compared to potent topical steroids. 1
First-Line Treatment Approach
Topical Calcineurin Inhibitors (Preferred)
- Tacrolimus 0.1% ointment or pimecrolimus 1% cream should be applied to affected areas twice daily for 8-12 weeks 2, 1
- These agents achieve nearly 50% repigmentation for facial and truncal lesions, with better side-effect profiles than highly potent topical corticosteroids 2
- Stinging is the primary side effect but is generally well-tolerated 2
- In children with hypopigmentation, calcineurin inhibitors are specifically recommended over potent steroids due to their better short-term safety profile 2
Alternative First-Line: Topical Corticosteroids
- Highly potent topical corticosteroids (such as clobetasol) can achieve similar repigmentation rates to calcineurin inhibitors 2
- However, they carry greater risk of skin atrophy, telangiectasia, and other steroid-related adverse effects, particularly with facial application 2
- Reserve for body sites where calcineurin inhibitor side effects are problematic 2
Second-Line Treatment for Inadequate Response
Phototherapy Options
- Narrowband UVB therapy is effective for generalized hypopigmentation, though results vary by anatomical location 1, 3
- Excimer laser (308 nm) combined with topical tacrolimus enhances repigmentation beyond UV therapy alone, particularly for UV-sensitive facial sites 2, 1
- Avoid UV therapy over bony prominences where response is poor 2
- Treatment should be administered 2-3 times weekly until repigmentation plateaus 3
Combination Therapy
- Adding Excimer UV radiation to topical tacrolimus provides superior results compared to either modality alone for facial lesions 2, 1
- This combination is particularly effective for treatment-resistant cases after 8-12 weeks of topical therapy alone 1
Third-Line Treatment for Resistant Cases
Procedural Interventions
- Surgical grafting techniques (punch grafting, split-thickness grafting, or autologous melanocyte transplantation) may be considered for stable, localized hypopigmentation that has not responded to medical therapy 3, 4
- These procedures are only appropriate for stable disease (no progression for at least 6-12 months) 3
- Laser therapy carries significant risks including persistent erythema and paradoxical worsening of hypopigmentation, and should be used with extreme caution 1
Treatment Algorithm
- Weeks 0-12: Apply topical tacrolimus 0.1% or pimecrolimus 1% twice daily 1
- Assess at 8-12 weeks: If <25% repigmentation, add narrowband UVB or Excimer laser 2-3 times weekly 1
- Assess at 24 weeks: If still inadequate response and disease is stable, consider surgical grafting options 3
Critical Monitoring Points
- Evaluate treatment response every 4-8 weeks using standardized photography in natural and Wood's lamp lighting 2, 1
- Wood's lamp examination helps delineate areas of pigment loss and assess repigmentation that may not be visible in natural light 2
- Discontinue treatment if no improvement after 16 weeks of combination therapy, as further treatment is unlikely to be beneficial 1
Important Cautions and Pitfalls
- Avoid dermabrasion and ablative laser techniques as they carry significant risk of worsening hypopigmentation and causing persistent erythema 1
- Most post-inflammatory hypopigmentation improves spontaneously within weeks to months if the inciting cause is removed 5
- Complete destruction of melanocytes results in permanent hypopigmentation that will not respond to medical therapy 5
- Chemical peels are contraindicated for hypopigmentation as they risk further pigment loss 1
Adjunctive Measures
- Apply moisturizers containing urea or glycerin to prevent excessive dryness that may impair repigmentation 1
- Strict photoprotection with broad-spectrum SPF 30+ sunscreen prevents further contrast between affected and unaffected skin 3
- Address any underlying inflammatory dermatoses (atopic dermatitis, psoriasis, etc.) that may perpetuate pigment loss 5