Download A4Medicine Mobile App
Empower Your RCGP AKT Journey: Master the MCQs with Us! 🚀
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.... | 
Try our Free Plan to get the full article.