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DISORDERS
Complex :
Genetic predisposition.
Precipitating factors.
Clinical Manifestation
Macula has a chalk or
milk-white color.
Several variation :
Trichrome vitiligo.
Quadrichrome vitiligo.
Pentachrome vitiligo.
Inflammatory vitiligo.
Hypopigmentation maculas on the face, neck and
Chest
Hipopigmentation on the glans penis
Hypopigmentation macula on the finger
Morbus Hansens tuberculoid type
Hypopigmentation maculas of Tinea versicolor
Hypopigmentation maculas of Tinea
Hypopigmentation maculas of Idiopathic guttate
hypomelanosis
Types of Vitiligo
1. Focal vitiligo.
2. Segmental vitiligo
3. Generalized vitiligo.
1 - 2% of the population
(0.14 - 8.8%).
Prevalence
All races are affected.
melanocytes.
Langerhans cell no
increased.
Pathogenesis
Autoimmunity.
Neurohumoral.
Anamnesis.
Clinical manifestation.
Histopathology.
Treatment
Spontaneus repigmentation (15 - 25%).
Psoralen ultra violet A (PUVA):
repigmentation (50 70%).
Systemic steroid.
Surgical therapy.
INTRODUCTION
Definition
Also known as chloasma
Melasma a common aquired
symetrical hypermelanosis characterized
by irregular light-brown to grey brown
macules and patches on sun-exposed
areas of the skin.
EPIDEMIOLOGY
Type of hypermelanosis:
- brown (epidermal)
- blue-grey (dermal)
- brown-grey (mixed)
Woods lamp examination
Epidermal type: lesions of contrast with
around normal skin
Dermal type : lesions of no contrast with
around normal skin
Mixed type : there are lesions contrast
or no with around normal
TREATMENT
The principles of therapy :
Protection from sunlight
Inhibition of the activity of melanocytes
Inhibition of the synthesis of melanin
Removal of melanin
Disruption of melanin granules
TREATMENT