INTRODUCTION
Acne vulgaris is a multifactorial, chronic, relapsing dermatosis primary of the face and trunk. It is most commonly observed in adolescents and young adults and frequently results in significant social, psychological, and physical consequences. Its prevalence rates are estimated to range from 35% to over 90% among adolescents.1 The natural course of this disease can commence as early as ages 7 to 12 (preadolescent acne) and, in many patients, fails to resolve until the third decade of an individual's life.2-4 As well as persisting for several decades, acne can develop for the first time during adulthood; this post-adolescent persistent or last-onset acne predominantly affects females.2,3,5
The primary clinical lesions seen in acne, ranging from open and closed comedones to papules, pustules, and large nodulocystic lesions, carry material physical and psychosocial morbidity, as do the clinical sequelae, which commonly arise from acne and include persistent erythema, acne-induced hyperpigmentation (PIH)/pigment alteration (PIPA) and scar formation. These sequelae correlate with the duration of acne, highlighting the necessity to initiate timely and effective treatment.2,5-10 Some evidence suggests that certain racial and ethnic groups may experience variations in the severity, prevalence, and sequelae of acne, with patients with skin of color being more likely to develop PIPA.1,11
The primary clinical lesions seen in acne, ranging from open and closed comedones to papules, pustules, and large nodulocystic lesions, carry material physical and psychosocial morbidity, as do the clinical sequelae, which commonly arise from acne and include persistent erythema, acne-induced hyperpigmentation (PIH)/pigment alteration (PIPA) and scar formation. These sequelae correlate with the duration of acne, highlighting the necessity to initiate timely and effective treatment.2,5-10 Some evidence suggests that certain racial and ethnic groups may experience variations in the severity, prevalence, and sequelae of acne, with patients with skin of color being more likely to develop PIPA.1,11