Pigmentary Skin Disorder Flashcards
What determines skin color?
The amount of melanin in the skin.
What are the types of pigmentary skin disorders?
Albinism, vitiligo, melasma, post-inflammatory hyperpigmentation, hyperpigmentation, hypopigmentation.
What is vitiligo?
An acquired pigmentary disorder characterized by circumscribed, depigmented macules and patches.
Which autoimmune disorder is most strongly associated with vitiligo?
Thyroid disease.
What is the prevalence of vitiligo?
Affects 0.5-2% of the population.
Which racial group has the lowest prevalence of vitiligo?
Han Chinese people.
At what age does vitiligo typically begin?
20-24 years, but can occur at any age.
How is vitiligo inherited?
Polygenic with a 23% monozygotic twin concordance.
Which autoimmune diseases are associated with vitiligo?
Thyroid disease, rheumatoid arthritis, IDDM, pernicious anemia, Addison’s disease, systemic lupus erythematosus (SLE).
How does vitiligo typically present?
White or depigmented macules and patches, well-demarcated, round, oval, or linear in shape.
Where does vitiligo most commonly appear?
Hands, forearms, feet, face (perioral, periocular).
What diagnostic tests are used for vitiligo?
Clinical exam, Wood’s lamp, skin biopsy, thyroid function tests, ANA, B12 levels.
What are the goals of vitiligo treatment?
Stop progression (stabilization) and achieve repigmentation.
Which areas of the body respond poorly to vitiligo treatment?
Hands, feet, and areas with white hair.
What topical treatments are used for vitiligo?
Corticosteroids, calcineurin inhibitors (tacrolimus, pimecrolimus), vitamin D derivatives (calcipotriol).
What systemic therapies are used for vitiligo?
Systemic steroids, methotrexate, mycophenolate mofetil, oral minocycline.
What surgical options exist for vitiligo?
Depigmentation therapy, skin grafting.
How does trauma affect vitiligo?
Cuts, grazes, or scratches may trigger new vitiligo patches.
What psychosocial support is recommended for vitiligo patients?
Counseling, cosmetic camouflage, and support groups.
What is albinism?
A condition with little or no melanin pigment in the eyes, skin, or hair.
What are the two main types of albinism?
Oculocutaneous albinism (OCA) and ocular albinism (OA).
Which enzyme is deficient in albinism?
Tyrosinase.
How is albinism inherited?
Mostly autosomal recessive.
What is the estimated carrier rate for albinism?
About 1 in 70 people carry a gene for albinism.