Diseases of Hypopigmentation / Depigmentation
- Hypopigmentation: lighter color
- Depigmentation: no color
Condition | Mechanism | Presentation | Key Finding |
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Vitiligo | Autoimmune → Absent melanocytes | DEpigmented (milk-white) patches | Autoimmune dz association |
Oculocutaneous Albinism (OCA) | Genetic defect → Non-fxn melanocytes | Diffuse hypopigmentation (skin/hair/eyes) | Nystagmus, ↓ visual acuity |
Phenylketonuria (PKU) | Enzyme defect → ↓ Melanin synthesis | Diffuse hypopigmentation (fair skin/hair) | Intellectual disability, musty odor |
Post-inflammatory Hypopigmentation | Inflammation → ↓ Melanin transfer | HYPOpigmented patches, follows prior rash | Hx of preceding dermatosis |
Diseases of Hyperpigmentation
Condition | Mechanism | Presentation | Key Finding |
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Melanoma | Malignant proliferation of melanocytes | Asymmetric, irregular border, variable color, >6 mm | Breslow depth is key prognostic factor |
Melasma | ↑ Melanin production (normal cell #) | Symmetric hyperpigmented patches on face | Linked to pregnancy, OCPs |
Nevus (Mole) | Benign proliferation of melanocytes | Symmetrical, uniform color, sharp border, <6 mm | Histology: Nests of nevus cells |
Solar Lentigo | Benign hyperplasia of melanocytes | Brown macules on sun-exposed areas (hands, face) | “Age spots”; do not fade in winter |
Ephelis (Freckle) | ↑ Melanin production (normal cell #) | Small macules on sun-exposed areas | Fades in winter, darkens in summer |