Psoriasis is a common skin disease in infants, children, and adolescents. A
review of the clinical, epidemiologic, genetic, and therapeutic aspects of
childhood psoriasis is presented. Population studies indicate that the fir
st signs of psoriatic lesions occur in the pediatric age group, birth to 18
years of age, and that both genetic and environmental factors interact to
precipitate the development of psoriasis. Koebner reactions are the result
of external or internal triggering factors, such as physical injury to the
skin, low humidity and certain drugs. The most frequently observed variant
of psoriasis is the plaque type, followed by guttate psoriasis, and juvenil
e psoriatic arthritis. Pustular psoriasis and erythrodermic psoriasis are r
are forms of the disease, but are seen in children from infancy to adolesce
nce. The scalp is the most frequently affected site of involvement in pedia
tric psoriasis, followed by the appearance of lesions on the extensor surfa
ces of the extremities trunk, and nails. Although not common in adult psori
asis, the face and ears are often involved. Topical medications such as cor
ticosteroids, calcipotriol, coal tar preparations, anthralin formulations,
and ultraviolet B are recommended in monotherapy or in combination therapy
whereas psoralen plus ultraviolet A, methotrexate, and retinoids should onl
y be administered in crisis situations. The treatment objectives in childho
od psoriasis are to preserve skin surfaces, to afford physical relief from
the disease, and to employ treatments that do not endanger the health or fu
ture development of the child.