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Updated: Jan 16, 2026

Quantification of Hypopigmentation Activity In Vitro
Published on: March 6, 2019
Common Causes of Hypopigmentation in Children
Paige Kingston1, Madison Jones2, Minnelly Luu2,3
1Olive View-UCLA Medical Center, Sylmar, California.
Insights
Hypopigmentation and depigmentation in children are common skin conditions. This review covers their causes, features, and management, distinguishing benign conditions from those needing specialist evaluation.
Area of Science:
- Pediatric Dermatology
- Genetics
- Dermatology
Background:
- Hypopigmentation (decreased) and depigmentation (complete loss) of skin pigment are common in children.
- Acquired causes include post-inflammatory changes, pityriasis alba, vitiligo, tinea versicolor, and halo nevi.
- Congenital causes may involve pigmentary mosaicism, which can be isolated or part of genetic syndromes like tuberous sclerosis complex.
Purpose of the Study:
- To review common causes of hypopigmentation and depigmentation in pediatric patients.
- To provide guidance on differentiating features, natural history, prognosis, and initial treatment.
- To identify indications for specialist referral and further investigation.
Main Methods:
- Literature review of common pediatric hypopigmentation and depigmentation disorders.
- Synthesis of information on clinical presentation, etiology, and management strategies.
- Focus on conditions encountered by general pediatricians.
Main Results:
- Most pediatric hypopigmentation and depigmentation cases are benign.
- Key acquired causes include pityriasis alba and vitiligo.
- Congenital conditions like nevus depigmentosus and syndromic pigmentary mosaicism require careful assessment.
Conclusions:
- Accurate diagnosis of pediatric hypopigmentation is crucial for appropriate management.
- While many conditions are benign, awareness of rare syndromic associations is important.
- Pediatricians should be able to differentiate common causes and know when to refer to a specialist.
Abstract:
Disorders of hypopigmentation are relatively common in children. Hypopigmentation refers to decreased pigmentation compared with surrounding skin, and depigmentation refers to a complete loss of pigmentation. The most common acquired causes include post-inflammatory hypopigmentation, pityriasis alba, vitiligo, tinea versicolor, and halo nevi. Commonly, congenital hypopigmented lesions may be attributed to pigmentary mosaicism, a term that refers to hypo- or hyperpigmentation resulting from somatic mosaicism. Pigmentary mosaicism most commonly occurs without syndromic association, such as in the case of nevus depigmentosus; however, rarely it can occur as part of a syndrome that may require further workup with genetic testing, such as with the hypomelanotic macules of tuberous sclerosis complex. Although most of the conditions causing hypopigmentation and depigmentation in children are benign, rare instances may be associated with syndromes or rare dermatoses that require further workup by a specialist. Given their common presentation to the general pediatrician, this article aims to cover the most common causes of hypo- and depigmentation in children, along with their differentiating features, natural history and prognosis, first-line treatment, and indications for further evaluation.
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