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Blistering Skin Disorders


Pemphigoid

Physician developed and monitored.

Original Date of Publication: 01 Sep 2000
Reviewed by: Stanley J. Swierzewski, III, M.D.

Original Source: http://www.dermatologychannel.net/blistering/pemphigoid.shtml

Home » Blistering Skin Disorders » Pemphigoid

Overview



Bullous (meaning "related to blisters") pemphigoid is a blistering disease that is seen most commonly in elderly persons. Unlike pemphigus, where loose and broken blisters are seen, pemphigoid produces large, tense blisters of the skin and, rarely, the mucous membranes. Blisters form when the patient's own antibodies (immune proteins) attack a specific layer in the skin, causing a separation between layers where fluid accumulates. In pemphigoid, this separation occurs between deeper layers of the skin, and, as a result, the blisters are stronger and don't break as easily.

Cause

Most cases of pemphigoid occur without a known inciting cause.

Signs and Symptoms

The skin blisters of pemphigoid are characteristically large and tense. They usually are seen on top of reddened skin and commonly appear on the abdomen, thighs, and forearms. Mucous membrane involvement is seen in fewer than one-third of patients.



Diagnosis

The clinical presentation of pemphigoid can be quite distinct. Laboratory confirmation is obtained by skin biopsy for routine pathological examination and for specialized immunofluorescence, a procedure that identifies which of the patient's antibodies is present in the skin, thus distinguishing it from other blistering diseases.

Treatment

Localized areas can be treated with topical corticosteroids alone. With extensive disease, oral corticosteroids are used, sometimes with the addition of other immune-suppressing drugs. Some studies report successful treatment using the antibiotic tetracycline and the vitamin nicotinamide (niacinamide, a B complex vitamin).

Prognosis

Pemphigoid is often self-limiting and may resolve within months, or it may last years.

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