Table 2.
Differential diagnosis of vitiligo (1,57) .
Inherited or genetically induced hypomelanoses(usually present at birth) |
|
Piebaldism |
|
Tuberous sclerosis |
|
Ito's hypomelanosis |
|
Waardenburg's syndrome |
|
Hermanski-Pudlak syndrome |
|
Menkés syndrome |
|
Ziprkowski-Margolis syndrome |
|
Griscelli's syndrome |
|
Post-inflammatory hypomelanoses |
|
Related to an increased epidermal turn over |
|
Psoriasis |
|
Atopic dermatitis |
|
Related to an acute lichenoid/cytotoxic infiltrate with pigment incontinence |
|
Lichen planus |
|
Toxic drug reaction |
|
Para-malignant hypomelanoses |
|
Mycosis fungoides |
|
Melanoma-associated depigmentation |
|
Para-infectious hypopigmentation |
|
Pityriasis versicolor |
|
Leprosy |
|
Leishmaniasis |
|
Onchocerciasis |
|
Acquired macular hypomelanosis |
|
Post traumatic leucoderma |
|
Post-burns |
|
Post-scars |
|
Melasma |
|
Occupational and drug induced depigmentation |
|
Phenolic-catecholic derivatives |
|
Systemic drugs(chloroquine, fluphenazine, physostigmine, imatinib) |
|
Topical drugs (imiquimod, long-term use of topical steroid) |
|