ANSWER: KERATOSIS PILARIS
Keratosis pilaris is a disorder of keratinization of the infundibulum of pilosebaceous follicles that results in horny plugs that fill the follicular orifice.1
Keratosis pilaris is a very common disorder: 40% of the population is affected.2 It develops during childhood and reaches its peak during adolescence. The prevalence in adolescents of both sexes is estimated to be at least 50%, while up to 80% of adolescent girls may be affected.2,3 The disorder involutes spontaneously and is less common during adult life.1,2 There is no racial predominance.4,5
ETIOLOGY
The exact cause is not known. An autosomal dominant mode of inheritance with incomplete penetrance has been postulated.2,3,5 The high prevalence and intensity seen at puberty suggest a hormonal influence. Hyperandrogenism in the presence of obesity is associated with an increased incidence and severity of keratosis pilaris.1
Keratosis pilaris is more common in patients with ichthyosis vulgaris and atopic dermatitis.3 Keratosis pilaris has also been reported to occur as a reaction to contact with cutting oil.6
Other conditions associated with keratosis pilaris include Cushing disease, hypothyroidism, vitamin A intoxication, vitamin C deficiency, monilethrix, Hodgkin disease, monosomy 18p, and cardio-facio-cutaneous syndrome.3,5,7,8 Given the high prevalence of keratosis pilaris, caution is suggested in the interpretation of these associations.3
PATHOLOGY
Measures should be taken to prevent excessive skin dryness. These include decreasing the frequency of skin cleansing; taking brief, tepid showers rather than long, hot baths; using mild soaps; and humidifying the home.3-5 In mild cases, an emollient—such as hydrophilic petrolatum—or a 10% to 20% urea cream usually alleviates the rough surface. More pronounced or widespread lesions may require treatment with a keratolytic agent, such as lactic acid, salicylic acid, or urea in combination with a topical corticosteroid or retinoic acid.9,10
The follicular orifice is distended by a keratotic plug that may contain twisted hairs.3
CLINICAL MANIFESTATIONS
Keratosis pilaris presents as minute, discrete, keratotic, follicular papules with variable perifollicular erythema.2 The lesions are not grouped and show no tendency to coalesce to form plaques. The affected skin looks like gooseflesh and feels like sandpaper. The lesions are not pruritic. Keratin plugs cannot be expressed with pressure and are usually painless.3,5 The lesions may be isolated or widespread; they have a predilection for the lateral aspects of the upper arms, thighs, and buttocks. The hands and feet are usually spared, but palmoplantar markings are more accentuated.
DIFFERENTIAL DIAGNOSIS
The differential diagnosis includes folliculitis, acne, phrynoderma, pityriasis rubra pilaris, and lichen spinulosus.3 The clinical features of keratosis pilaris are so distinct that usually there is little difficulty in diagnosis.