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DISORDERS
Pigmentary disoders:
- Hypomelanoses
- Hypermelanoses
Hypomelanoses:
- Piebaldism
- Idiopathic guttate
- Vitiligo
hypomelanoses
- Pinta
- drugs:
- Albinism
- arsenical
- Leprosy
- chloroquine
- Pityriasis alba
- hydroquinone
- Pityriasis versicolor
- retinoid
Hypermelanoses:
- Lentigines
- Nevus melanositic
- Berloque dermatitis - melasma
- Pityriasis versicolor -Berloque dermatis
- Drugs
- 5 Fluoro Uracil
- Cyclophosphamide
- Topical Bleomycine
VITILIGO
Definition
It
is
an
acquired,
often
manifested
by
Etiology
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.
Types of Vitiligo
1. Focal vitiligo.
2. Segmental vitiligo
3. Generalized vitiligo.
4. Other cutaneus abnormalities.
Incidence
1 - 2% of the population
(0.14 - 8.8%).
Prevalence
All races are affected.
years.
Histopathology
Absence of dopa-positive
melanocytes.
Langerhans
increased.
cell
no
Pathogenesis
Autoimmunity.
Neurohumoral.
Exogenous chemical exposures.
Diagnosis
Anamnesis.
Clinical manifestation.
Histopathology.
Treatment
Spontaneus repigmentation (15 - 25%).
Psoralen
ultra
violet
Systemic steroid.
Surgical therapy.
(PUVA):
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
Age of onset young adults
Sex Female >> male
(10% men )
Race more frequent in person with
brown or black constitutive skin
colour
ETIOLOGY
The precise cause is as yet unknown, but
the contributing factors include :
Genetic
Endocrine disfunction
Pregnancy
Drugs
Cosmetics
UltraViolet light
exposure
PATHOGENESIS
Unknown.
HISTOPATOLOGY
melanin
Basal and suprabasal higher than
normal level of melanin
Dermalblue-gray, melanin laden
macrophages occur in perivascular
superficial & mid-dermal
Epidermal
HISTOPATOLOGY
Ultrastructure
shows :
melanocytes
melanogenesis
Transfer of melanosomes
Size & percentage of melanosomes in
keratinocyte
PHYSICAL EXAMINATION
PHYSICAL EXAMINATION
Three typical patern of distribution :
Centrofacial : cheeks, forehead,
Clinical manifestation
Macular lesions:
- serrated
- irreguler
- geographic border
- usually symetry
Clinical manifestation:
Type of hypermelanosis:
- brown (epidermal)
- blue-grey (dermal)
- brown-grey (mixed)
TREATMENT
The
principles of therapy :
TREATMENT
Protection from sunlight
Sunscreen : Sun protection factor (SPF)
Cosmetics : acylglutamate (cleanser)
Systemic drug: chloroquin, Vit.C & E,
TREATMENT
Inhibition of the activity of
melanocytes
Avoiding :
Exposure to sunlight
Pregnancy
Birth control pills
Scented cosmetics
Phototoxic drugs
TREATMENT
Inhibition of the syntesis of
melanin
Topical hydroquinone 2% - 4%
Kojic acid 2 4 %
Azeleic acid 20 %.
TREATMENT
Removal of melanin
Trichloroacetic acid (TCA)
Jesners Solution
Glycolic acid 70 %
Disruption of melanin granules
Pigmented laser
DIFFERENTIAL DIAGNOSE
Post inflamatory hypermelanosit
Tinea Versicolor
Acquired brachial Cutaneus dyschromatos
Tar Melanosis
Pellagra
Photocontact dermatitis
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