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The following table outlines the differential diagnosis for hypopigmentation in dermatological settings. Recognizing that hypopigmentation can be a manifestation of various systemic and cutaneous conditions, this table aims to assist clinicians in effectively identifying and distinguishing among the numerous possibilities. Conditions such as vitiligo, tinea versicolor, and drug-induced hypopigmentation are among those discussed, each with its clinical relevance highlighted.
Differentials for Hypopigmentation | Clinical Information and Relevance |
---|---|
Vitiligo | Characterized by depigmented patches of skin; often symmetric. Associated with other autoimmune disorders. |
Pityriasis Alba | Common in children and adolescents; presents as pale patches, usually on the face. |
Tinea Versicolor | Fungal infection that disrupts normal pigmentation, usually causing hypopigmented patches. |
Post-inflammatory Hypopigmentation | Follows skin inflammation or injury; can occur after conditions like dermatitis or burns. |
Nevus Depigmentosus | Congenital condition presenting with stable, non-progressive hypopigmented patches. |
Albinism | Genetic condition causing a complete or partial absence of melanin. |
Leprosy | Infectious disease that can cause skin lightening along with other cutaneous and systemic symptoms. |
Hypopigmented Mycosis Fungoides | A rare variant of cutaneous T-cell lymphoma, presents with hypopigmented patches. |
Idiopathic Guttate Hypomelanosis | Characterized by small, round, hypopigmented macules; commonly observed on sun-exposed areas in older adults. |
Drug-induced Hypopigmentation | Caused by medications like corticosteroids, retinoids, or certain antimalarials.... |
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