Pigmentation
Skin colour is due to a mixture of the pigments melanin (p. 8), oxyhaemoglobin (in blood) and carotene (in the stratum corneum and subcutaneous fat). Pigmentary diseases are common and particularly distressing to those with darker skin. Disorders of pigmentation mainly involve melanocytes, but other causes are mentioned where relevant.
Hypopigmentation
Pigment loss may be generalized or patchy. Generalized hypopigmentation occurs with albinism, phenylketonuria and hypopituitarism; patchy loss is seen in vitiligo, after inflammation, following exposure to some chemicals and with certain infections (Table 1).
Cause | Example |
---|---|
Chemical | Substituted phenols, hydroquinone |
Endocrine | Hypopituitarism |
Genetic | Albinism, phenylketonuria, tuberous sclerosis, piebaldism |
Infection | Leprosy, yaws, pityriasis versicolor |
Postinflammatory | Cryotherapy, eczema, psoriasis, morphoea, pityriasis alba |
Other | Vitiligo, lichen sclerosus, halo naevus, scarring |
Vitiligo
Clinical presentation
Vitiligo affects 0.5% of the population, is seen in all races and is most troublesome in those with a dark skin. The sex incidence is equal, and the onset, usually between 10 and 30 years of age, may be precipitated by injury or sunburn. The sharply defined white macules are often symmetrical (Fig. 1). The hands, wrists, knees, neck and areas around orifices (e.g. the mouth) are frequently affected. Occasionally, vitiligo is segmental (e.g. down an arm), generalized or universal. The course is unpredictable; areas may remain static, spread or (infrequently) repigment. In light-skinned individuals, vitiligo may be discernible only in summer, when the non-vitiliginous areas become sun-tanned.
Differential diagnosis
Postinflammatory hypopigmentation is often accompanied by other skin changes (Table 1). In chemical leucoderma, a history of exposure to phenolic chemicals should be sought. The hypopigmented macules of leprosy are normally anaesthetic.
Albinism
There are several syndromes of albinism. All are autosomal recessive and show a lack of pigment in the skin, hair, iris and retina. Melanocyte numbers are normal, but melanosome production fails due to defective gene control of tyrosinase (p. 8).