Keratosis Pilaris Symptoms, Causes, Treatment - What causes KP? on MedicineNet

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February 10, 2012

Keratosis Pilaris (cont.)

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What causes KP?

The exact cause of KP is unknown. There seems to be a problem with overproduction of the keratin part of the skin called hyperkeratinization. KP is thought to be partly inherited (genetic) in origin. About 50%-70% of patients with KP have a known genetic predisposition and a high rate of affected family members. Many individuals have a strong family history of KP or "chicken skin." The underlying cause may partly be related to hypersensitivity reactions and overall dryness of the skin. KP is also closely related to ichthyosis vulgaris, dry skin, allergies, seasonal allergies, rhinitis, asthma, eczema, and atopic dermatitis.

The bumps in KP seem to arise from the excessive accumulation of keratin (very small, dry skin particles) at the opening of individual hair follicles. The skin as examined under the microscope demonstrates mild thickening, hyperkeratosis, and plugging of the hair follicle. The upper skin layers may have some dilation of the small superficial blood vessels, thereby giving the skin a red or flushed appearance.

How is keratosis pilaris diagnosed?

The diagnosis of KP is very straightforward and based on a typical skin appearance in areas like the upper arms. A family history of KP is also very helpful since there is a strong genetic component to the condition. The diagnosis is confirmed by the physician's clinical exam.

What else could it be?

Other medical conditions can mimic KP. KP may resemble acne, milia, folliculitis, eczema, atopic dermatitis, facial rosacea, or dry skin (xerosis). KP may also resemble uncommon skin conditions like lichen spinulosus, pityriasis rubra pilaris, phrynoderma (vitamin A deficiency), ulerythema ophryogenes, ichthyosis vulgaris, eruptive vellus hair cysts, keratosis follicularis (Darier disease), Kyrle disease, lichen nitidus, lichen spinulosus, perforating folliculitis, and trichostasis spinulosa.

In India and other countries, a specific condition called erythromelanosis follicularis faciei et colli occurs. This unusual condition has a possible genetic relationship to KP. Erythromelanosis follicularis faciei et colli is characterized by the triad of hyperpigmentation (darker skin color), follicular plugging (blocked hair follicles), and redness of the face and neck.

Are there any lab tests to help diagnose keratosis pilaris?

No specific laboratory tests aid in the diagnosis of KP. Imaging studies like X-rays and CT scans are not useful. Skin biopsy (surgically taking a small piece of skin using local numbing medicine) may be useful in atypical or widespread cases.

What does keratosis pilaris look like under the microscope?

Microscopic examination of the body tissue by a pathologist or dermatopathologist under high magnification is called histopathology or pathology. Histopathology of KP shows mild hyperkeratosis of the epidermis (thickening of the outer layer of skin), hypergranulosis (increase in the special granular cells of the epidermis), and plugging of individual hair follicles. The upper dermis (layer of the skin below the epidermis) may have some microscopic inflammation called mild superficial perivascular lymphocytic inflammatory changes.

Is keratosis pilaris curable?

There is no available cure, miracle pill, or universally effective treatment for KP. It sometimes clears completely by itself without treatment.

Is keratosis pilaris contagious?

KP is not contagious. It is not an infection and is not caused by a fungus, bacterium, or virus. People do not give it to someone else through skin contact and do not catch it from anyone else. Some people are simply more prone to developing KP because of genetics and skin type.

What are possible complications of keratosis pilaris?

Complications are infrequent since it's primarily a cosmetic skin condition. However, temporary skin discoloration called postinflammatory hypopigmentation (lighter than the regular skin color) or hyperpigmentation may occur after the inflamed, red bumps have improved or after a temporary flare. Permanent scarring may rarely occur from deep picking, overly aggressive treatments, or other inflammation.

Does diet have anything to do with keratosis pilaris?

Overall, diet does not seem to affect KP. Vitamin A deficiency may cause symptoms similar to KP, but it's not a known cause of KP.


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