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Dermatology

Vitiligo

Confirm true depigmentation, define nonsegmental versus segmental distribution and activity, screen selectively for autoimmune disease, and match topical, phototherapy, systemic, or surgical treatment to extent, site, progression, and stability.

Clinical question: How should clinicians confirm, phenotype, investigate, treat, and monitor vitiligo according to distribution, activity, extent, and anatomic site?

Initial assessment

Confirm depigmentation and classify the clinical pattern

The first management decision is whether the eruption is vitiligo and, if so, which distribution and activity pattern is present.

Diagnose typical vitiligo clinically when sharply demarcated, milky-white, non-scaly macules or patches are present. Examine all skin in natural light and with a Wood lamp before selecting therapy: lesions fluoresce blue-white, contrast is enhanced, and occult areas may become apparent. Record skin phototype, duration, body distribution, mucosal and hair involvement, and whether lesions are expanding; these features guide treatment selection and provide a baseline for response. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDAScienceDirectVitiligo

Classify bilateral or symmetric patches as nonsegmental vitiligo unless another diagnosis explains the pattern. Classify a predominantly unilateral distribution as segmental vitiligo. This distinction matters because ruxolitinib cream efficacy and safety were established in nonsegmental vitiligo, and NB-UVB has less supporting evidence for segmental or unclassifiable disease. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDAScienceDirectVitiligoPubMedSecond Guidelines for the Diagnosis and Treatment of Vitiligo in Japan (2025) - PMC

Use dermoscopy when clinical morphology or disease activity is uncertain, particularly when distinguishing vitiligo from other acquired hypopigmentary or depigmenting disorders. If the diagnosis remains uncertain after examination, biopsy a representative active edge rather than a fully depigmented center; vitiligo histology shows absent or near-absent epidermal melanocytes, while early lesions may show interface dermatitis with CD8-positive lymphocytes and lymphocytic infiltrates at the advancing border. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDA

Clinical pattern and its immediate management implication. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDAScienceDirectVitiligoPubMedSecond Guidelines for the Diagnosis and Treatment of Vitiligo in Japan (2025) - PMC
PatternFindings that support itWhat changes next
Nonsegmental vitiligoBilateral, often symmetric patches; generalized, acrofacial, or universal distribution may occur. ScienceDirectVitiligoAssess extent and activity; consider topical therapy for limited disease, NB-UVB for more extensive disease, and ruxolitinib cream only within its studied nonsegmental population. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDAPubMedSecond Guidelines for the Diagnosis and Treatment of Vitiligo in Japan (2025) - PMC
Segmental vitiligoUsually unilateral distribution. ScienceDirectVitiligoAssess stability carefully; phototherapy evidence is less robust, and stable lesions may be candidates for surgical repigmentation approaches. PubMedSecond Guidelines for the Diagnosis and Treatment of Vitiligo in Japan (2025) - PMCJAMASurgical Interventions for Patients With Vitiligo: A Systematic Review ...
Atypical or uncertain depigmentationMorphology, scale, distribution, or Wood lamp findings do not support a confident clinical diagnosis. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDAScienceDirectAcquired disorders with depigmentation: A systematic approach to ...Use dermoscopy and consider biopsy of an active border to evaluate melanocyte loss and inflammatory pattern before immunomodulatory treatment. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDAScienceDirectComparative study of dermatologists and deep learning model on diagnosing childhood vitiligo

Comorbidity workup

Screen for autoimmune thyroid disease and target further testing

Laboratory testing should identify clinically actionable autoimmune comorbidity without indiscriminate serologic panels.

For suspected nonsegmental vitiligo, obtain thyroid function tests and antithyroid antibodies to identify patients at increased risk for autoimmune thyroid disease. Vitiligo is associated with Hashimoto thyroiditis and Graves disease, and thyroid testing is recommended in adults and children with vitiligo. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDAnice org uk[PDF] National Institute for Health and Care Excellence - NICE

Do not order broad autoimmune antibody panels solely because vitiligo is present. Add testing for another autoimmune condition only when symptoms, examination, family history, or initial testing creates a specific diagnostic suspicion. An abnormal thyroid result should trigger management according to the thyroid disorder rather than alter vitiligo treatment automatically. nice org uk[PDF] National Institute for Health and Care Excellence - NICE

At each treatment review, reassess disease activity and quality-of-life effect rather than relying only on pigment change. Higher vitiligo activity and severity scores have been associated with greater quality-of-life impairment in patients with thyroid dysfunction, supporting closer follow-up when active disease and thyroid autoimmunity coexist. Wolters KluwerThyroid Dysfunction in Vitiligo Patients:... : Journal of Datta Meghe Institute of Medical Sciences University

Targeted investigation strategy in vitiligo. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDAnice org uk[PDF] National Institute for Health and Care Excellence - NICE
Clinical situationTest or actionInterpretation and next step
Suspected nonsegmental vitiligoThyroid function tests plus antithyroid antibodies. nice org uk[PDF] National Institute for Health and Care Excellence - NICEIdentify autoimmune thyroid disease or risk for future thyroid disease; manage an identified thyroid disorder through the appropriate pathway. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDAnice org uk[PDF] National Institute for Health and Care Excellence - NICE
Symptoms, family history, examination, or prior results suggesting another autoimmune conditionOrder condition-directed testing rather than a routine broad autoimmune screen. nice org uk[PDF] National Institute for Health and Care Excellence - NICEPursue the specific suspected autoimmune diagnosis and coordinate care as indicated. nice org uk[PDF] National Institute for Health and Care Excellence - NICE
Atypical lesions or diagnostic uncertaintyDermoscopy; biopsy of a representative lesion when needed. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDAScienceDirectComparative study of dermatologists and deep learning model on diagnosing childhood vitiligoAbsent epidermal melanocytes supports vitiligo; an alternative histologic pattern redirects the differential and treatment. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDA

Limited disease

Choose site-directed therapy for localized vitiligo

For limited involvement, select treatment by anatomic site, patient age, progression, and tolerance for local adverse effects.

Topical corticosteroids are a first-line option for focal, segmental, and localized vitiligo. Use a time-limited course because prolonged exposure can cause skin thinning; reassess clinical response and local toxicity rather than continuing indefinitely. Older consensus practice used moderately potent to potent corticosteroids for facial disease and potent to very potent agents for body lesions, but long-term topical corticosteroid treatment is not advocated because of adverse effects. PubMedVitiligo in adults and children - PMCaadVitiligo: Diagnosis and treatment - American Academy of Dermatology

Prefer tacrolimus ointment or pimecrolimus cream when lesions involve the face, neck, or body folds, where avoiding corticosteroid atrophy is a priority. Topical calcineurin inhibitors can be used longer than topical corticosteroids and are especially useful for head and neck lesions; counsel that transient application-site burning, itch, or irritation can occur. In a meta-analysis, burning occurred in 9.8%, pruritus in 7.4%, and erythema in 2.4% of patients treated with topical calcineurin inhibitor monotherapy. cks nice org ukScenario: Management of vitiligo - CKS - NICEaadVitiligo: Diagnosis and treatment - American Academy of DermatologyPubMedTreatment Outcomes of Topical Calcineurin Inhibitor Therapy for Patients With Vitiligo: A Systematic Review and Meta-analysis - PMC

Ruxolitinib 1.5% cream is a disease-directed topical option only for nonsegmental vitiligo, the population in which efficacy and safety were established. Confirm subtype before prescribing and reassess treatment response with standardized photography and Wood lamp examination; do not extrapolate the pivotal-population finding to segmental vitiligo as if equivalent evidence existed. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDA

Topical treatment selection by clinical context. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDAPubMedVitiligo in adults and children - PMCcks nice org ukScenario: Management of vitiligo - CKS - NICEaadVitiligo: Diagnosis and treatment - American Academy of DermatologyPubMedTreatment Outcomes of Topical Calcineurin Inhibitor Therapy for Patients With Vitiligo: A Systematic Review and Meta-analysis - PMC
Clinical contextPreferred optionKey limitation or monitoring issue
Localized nonfacial lesionsTime-limited topical corticosteroid therapy. PubMedVitiligo in adults and children - PMCaadVitiligo: Diagnosis and treatment - American Academy of DermatologyMonitor for skin thinning; avoid long-term continuous use. PubMedVitiligo in adults and children - PMCaadVitiligo: Diagnosis and treatment - American Academy of Dermatology
Face, neck, or body foldsTacrolimus ointment or pimecrolimus cream. cks nice org ukScenario: Management of vitiligo - CKS - NICEaadVitiligo: Diagnosis and treatment - American Academy of DermatologyCounsel regarding burning, pruritus, and local irritation. aadVitiligo: Diagnosis and treatment - American Academy of DermatologyPubMedTreatment Outcomes of Topical Calcineurin Inhibitor Therapy for Patients With Vitiligo: A Systematic Review and Meta-analysis - PMC
Nonsegmental vitiligo appropriate for topical JAK inhibitionRuxolitinib 1.5% cream. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDAEvidence base is for nonsegmental vitiligo; document subtype before treatment. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDA
Suboptimal response to topical calcineurin inhibitor aloneAdd NB-UVB or excimer-based phototherapy where available. PubMedTreatment Outcomes of Topical Calcineurin Inhibitor Therapy for Patients With Vitiligo: A Systematic Review and Meta-analysis - PMCWolters KluwerPhototherapy in vitiligo : Pigment InternationalResponse varies substantially; monitor repigmentation with consistent baseline and follow-up assessment. Wolters KluwerPhototherapy in vitiligo : Pigment InternationalPubMedTreatment Outcomes of Topical Calcineurin Inhibitor Therapy for Patients With Vitiligo: A Systematic Review and Meta-analysis - PMC

Escalation

Use phototherapy for extensive disease and suppress rapidly progressive activity

Extent and active spread determine whether topical treatment alone is insufficient.

For nonsegmental vitiligo involving 10% to 40% body surface area, systemic NB-UVB is recommended as first-line therapy in adults and children older than 10 years. NB-UVB has largely replaced PUVA for lesions affecting at least 10% of skin surface area because it has no systemic toxicity and has favorable safety in children and adults. Expect perifollicular repigmentation after approximately 15 to 20 sessions; continue therapy when pigmentation is progressing, with courses extending beyond 9 to 12 months and, in selected responders, up to 24 months followed by gradual dose reduction. PubMedSecond Guidelines for the Diagnosis and Treatment of Vitiligo in Japan (2025) - PMC

Choose targeted UVB or excimer laser/light for circumscribed lesions when whole-body NB-UVB is disproportionate to disease extent. Once-weekly targeted UVB may be as effective as twice-weekly therapy for lesions of the face, neck, torso, limbs, and scalp, but initial repigmentation may occur more slowly with the less frequent schedule. Wolters KluwerPhototherapy in vitiligo : Pigment International

For highly progressive vitiligo, refer promptly to dermatology for systemic disease-stabilizing treatment rather than escalating topical therapy alone. A described regimen is methylprednisolone 16 mg or dexamethasone 5 mg on two consecutive days weekly for 3 to 6 months, combined with NB-UVB two to three times weekly for 6 months. This approach is reported to block relapse in more than 80% of cases, but systemic corticosteroid exposure requires individualized risk assessment and pediatric review after 3 months in growing children. PubMedVitiligo: Current Therapies and Future Treatments

Do not equate stabilization with durable remission. After treatment cessation, approximately 40% of patients have some pigment loss within one year. For patients who repigment, plan maintenance topical therapy several times weekly when appropriate and continue objective surveillance for recurrent activity. aadVitiligo: Diagnosis and treatment - American Academy of Dermatology

Escalation by vitiligo extent and activity. Wolters KluwerPhototherapy in vitiligo : Pigment InternationalPubMedSecond Guidelines for the Diagnosis and Treatment of Vitiligo in Japan (2025) - PMCPubMedVitiligo: Current Therapies and Future TreatmentsaadVitiligo: Diagnosis and treatment - American Academy of Dermatology
Disease stateTreatment approachTiming and reassessment
Nonsegmental vitiligo involving 10% to 40% body surface areaWhole-body NB-UVB. PubMedSecond Guidelines for the Diagnosis and Treatment of Vitiligo in Japan (2025) - PMCLook for follicular repigmentation after 15 to 20 sessions; continue responsive treatment beyond 9 to 12 months when benefit persists. PubMedSecond Guidelines for the Diagnosis and Treatment of Vitiligo in Japan (2025) - PMC
Circumscribed lesions needing light treatmentTargeted UVB or excimer laser/light. Wolters KluwerPhototherapy in vitiligo : Pigment InternationalOnce-weekly treatment may delay initial visible restoration compared with twice-weekly treatment. Wolters KluwerPhototherapy in vitiligo : Pigment International
Highly progressive diseaseSystemic corticosteroid mini-pulse plus NB-UVB two to three times weekly. PubMedVitiligo: Current Therapies and Future TreatmentsSystemic mini-pulses are described for 3 to 6 months; obtain pediatric input after 3 months in growing children. PubMedVitiligo: Current Therapies and Future Treatments
Repigmented disease after treatment withdrawalTopical maintenance medication several times weekly when appropriate. aadVitiligo: Diagnosis and treatment - American Academy of DermatologyMonitor for recurrence because about 40% experience some color loss within one year after treatment ends. aadVitiligo: Diagnosis and treatment - American Academy of Dermatology

Refractory disease

Refer stable, treatment-refractory lesions for surgical repigmentation assessment

Surgery is a lesion-directed option after stability, not a rescue strategy for ongoing inflammatory spread.

Consider surgical repigmentation procedures for stable vitiligo that remains cosmetically significant despite medical treatment, particularly segmental disease or focal stable lesions. Available approaches include tissue grafting and cellular grafting techniques; a systematic review and meta-analysis evaluated treatment response across surgical modalities, supporting surgery as a distinct management pathway rather than an extension of topical therapy. JAMASurgical Interventions for Patients With Vitiligo: A Systematic Review ...

Before surgical referral, reconfirm lesion stability with serial clinical and Wood lamp photographs and exclude active expansion. Persistent inflammatory activity, new lesions, or trauma-associated spread should redirect management toward disease stabilization, typically phototherapy with or without systemic therapy for highly progressive disease, rather than grafting into an active disease field. fda[PDF] NDA 215309/S‐001 Opzelura (ruxolitinib) cream, 1.5% - FDAWolters KluwerThyroid Dysfunction in Vitiligo Patients:... : Journal of Datta Meghe Institute of Medical Sciences UniversityPubMedVitiligo: Current Therapies and Future Treatments

Use dermoscopy and Wood lamp examination as adjuncts when monitoring postoperative repigmentation. Evaluate both pigment gain and recurrence at lesion edges; repeat grafting decisions should be based on durable stability and objective repigmentation rather than a single follow-up appearance. ScienceDirectAnalysis of dermoscopic characteristics in vitiligo lesions treated ...

When to change from medical to procedural management. JAMASurgical Interventions for Patients With Vitiligo: A Systematic Review ...ScienceDirectAnalysis of dermoscopic characteristics in vitiligo lesions treated ...PubMedVitiligo: Current Therapies and Future Treatments
FindingManagement decisionReason
New or enlarging lesions, or other evidence of highly progressive diseaseDo not proceed directly to surgery; prioritize stabilization with dermatology-directed systemic mini-pulse therapy and NB-UVB when indicated. PubMedVitiligo: Current Therapies and Future TreatmentsSurgical repigmentation is best considered in stable disease rather than an actively spreading disease field. JAMASurgical Interventions for Patients With Vitiligo: A Systematic Review ...PubMedVitiligo: Current Therapies and Future Treatments
Stable focal or segmental lesions with inadequate medical responseRefer for consideration of tissue or cellular grafting techniques. JAMASurgical Interventions for Patients With Vitiligo: A Systematic Review ...Surgical modalities are established options for selected stable vitiligo. JAMASurgical Interventions for Patients With Vitiligo: A Systematic Review ...
Postoperative pigment assessmentUse dermoscopy as an adjunct to Wood lamp examination. ScienceDirectAnalysis of dermoscopic characteristics in vitiligo lesions treated ...These tools support objective assessment of repigmentation. ScienceDirectAnalysis of dermoscopic characteristics in vitiligo lesions treated ...

References

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