How do you differentiate pityriasis alba from vitiligo?

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Differentiating Pityriasis Alba from Vitiligo

Pityriasis alba presents with ill-defined, hypopigmented (not depigmented) patches with fine scaling and preserved melanocytes on histology, while vitiligo shows well-demarcated, completely depigmented (chalk-white) patches with complete loss of melanocytes that enhance dramatically under Wood's light examination.

Clinical Examination Features

Pigmentation Characteristics

  • Pityriasis alba shows incomplete hypopigmentation with indistinct, poorly defined borders that blend gradually into surrounding normal skin 1, 2
  • Vitiligo demonstrates complete depigmentation appearing chalk-white with sharply demarcated borders, particularly evident in classical symmetrical presentations 3
  • The degree of pigment loss is the most critical distinguishing feature: pityriasis alba retains some pigment while vitiligo shows total absence 1, 4

Surface Changes

  • Pityriasis alba consistently presents with fine scaling and a slightly rough texture, often with follicular papules in early stages 2, 5
  • Vitiligo has smooth surface without scaling, as it represents pure melanocyte loss without epidermal disruption 3, 6

Hair Involvement

  • Pityriasis alba shows normally pigmented hairs within the hypopigmented patches 2
  • Vitiligo frequently demonstrates leucotrichia (white hairs) within depigmented areas, indicating follicular melanocyte destruction 6

Wood's Light Examination

  • Vitiligo lesions enhance dramatically under Wood's light, appearing bright white due to complete absence of melanin, making this examination particularly useful for diagnosis and monitoring 3
  • Pityriasis alba shows minimal to no enhancement under Wood's light because melanin is reduced but not absent 4, 2

Distribution Patterns

Pityriasis Alba

  • Predominantly affects the face (especially cheeks), arms, and forearms 5
  • More commonly detected in children and adolescents with darker skin types 4, 2
  • Lesions may be solitary (16% of cases) or multiple 1

Vitiligo

  • Classical presentations show symmetrical distribution affecting fingers, wrists, axillae, groins, and body orifices (mouth, eyes, genitalia) 7, 8
  • Can present as segmental (unilateral, following dermatomes) or non-segmental (symmetrical) patterns 7, 8
  • Diagnosis is straightforward in symmetrical presentations but atypical cases require dermatologist assessment 3

Dermoscopic Features

Pityriasis Alba

  • White structureless spots with indistinct borders 2
  • Fine scaling consistently present 2
  • Normally pigmented hairs within lesions 2
  • Faint pigmented network may be visible (27.5% of cases) 2
  • Areas of light brown pigmentation (42.5% of cases) 2

Vitiligo

  • Reduced or absent pigment network in lesional center 6
  • Perifollicular pigmentation patterns indicating disease activity or treatment response 6
  • Sharp borders in stable disease; diffuse borders, trichrome pattern, or "comet tail" phenomenon in active disease 6
  • Marginal hyperpigmentation common in pigmented lesions 6

Histopathological Differentiation

Pityriasis Alba

  • Melanocyte count remains normal between lesional and non-lesional skin—this is the definitive histologic distinction 1
  • Markedly reduced melanin pigment in epidermis despite normal melanocyte numbers 1
  • Follicular plugging, follicular spongiosis, and atrophic sebaceous glands 5
  • Degenerative changes in melanocytes with reduced melanosomes in keratinocytes 1

Vitiligo

  • Complete loss of functioning epidermal melanocytes in affected areas 7, 8
  • Progressive melanocyte destruction, not just dysfunction 8

Associated Conditions

Pityriasis Alba

  • History of atopic dermatitis in 18% of patients 1
  • Associated with xerosis and poor cutaneous hydration 4
  • No systemic associations 4, 5

Vitiligo

  • Autoimmune thyroid disease in approximately 34% of adults—thyroid function testing is specifically recommended by the British Journal of Dermatology guidelines 7
  • Other autoimmune conditions frequently associated 7
  • Familial trait in about 18% of cases 3

Common Diagnostic Pitfalls

  • Failing to use Wood's light examination in patients with lighter skin types where vitiligo may be subtle 3
  • Confusing early-stage pityriasis alba (with erythematous papules) with inflammatory conditions 5
  • Missing the psychological impact of vitiligo, which significantly affects quality of life and requires assessment 3, 7
  • Not screening for thyroid disease in vitiligo patients, missing a treatable autoimmune condition present in one-third of cases 7
  • Overlooking the need for dermatologist referral when vitiligo presents atypically 3

Clinical Algorithm for Differentiation

  1. Assess pigment loss degree: Complete (vitiligo) vs. incomplete (pityriasis alba) 1, 4
  2. Check for scaling: Present (pityriasis alba) vs. absent (vitiligo) 2, 5
  3. Perform Wood's light exam: Dramatic enhancement (vitiligo) vs. minimal/none (pityriasis alba) 3, 4
  4. Examine hair within lesions: White hairs (vitiligo) vs. normally pigmented (pityriasis alba) 6, 2
  5. Evaluate borders: Sharp demarcation (vitiligo) vs. indistinct (pityriasis alba) 1, 2
  6. If vitiligo confirmed: Check thyroid function given 34% prevalence of autoimmune thyroid disease 7

References

Research

Clinical and histopathological characteristics of pityriasis alba.

Clinical and experimental dermatology, 2009

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Pityriasis alba: a histologic study.

International journal of dermatology, 1993

Research

Dermatoscopic Patterns in Vitiligo.

Dermatology practical & conceptual, 2023

Guideline

Autoimmune Connection in Vitiligo and Erythema Annulare Centrifugum

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Pathogenesis of Vitiligo

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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