Merck Manual

Please confirm that you are a health care professional

honeypot link

Pemphigus Foliaceus


Daniel M. Peraza

, MD, Geisel School of Medicine at Dartmouth University

Last full review/revision Sep 2020| Content last modified Sep 2020
Click here for Patient Education
Topic Resources

Pemphigus foliaceus is an autoimmune blistering disorder in which lack of adhesion in the superficial epidermis result in cutaneous erosions. Diagnosis is by skin biopsy and direct immunofluorescence. Treatment depends on disease severity and includes topical or systemic corticosteroids. Other immunosuppressive therapies may be needed.

Bullae are elevated, fluid-filled blisters ≥ 10 mm in diameter.

Pemphigus foliaceus usually occurs in middle-aged patients, affecting men and women in equal numbers. An endemic form of pemphigus foliaceus, fogo selvagem, occurs in younger adults and children, particularly in South America. Pemphigus foliaceus may occur after use of penicillamine, nifedipine, or captopril.

Pemphigus erythematosus, a form of pemphigus foliaceus localized to the cheeks, has immunologic features of pemphigus and lupus erythematosus Systemic Lupus Erythematosus (SLE) Systemic lupus erythematosus is a chronic, multisystem, inflammatory disorder of autoimmune etiology, occurring predominantly in young women. Common manifestations may include arthralgias and... read more Systemic Lupus Erythematosus (SLE) (IgG and C3 deposition on keratinocyte surfaces and basement membrane zone with circulating antinuclear antibodies); however, patients rarely are diagnosed with both diseases concurrently.

Skin cleavage levels in pemphigus and bullous pemphigoid

Pemphigus foliaceus blisters form in the superficial layers of the epidermis. Pemphigus vulgaris blisters can form at any epidermal level but typically form in the lower aspects of the epidermis. Bullous pemphigoid blisters form subepidermally (lamina lucida of the basement membrane zone). In this figure, the basement membrane zone is disproportionately enlarged to display its layers.

Skin cleavage levels in pemphigus and bullous pemphigoid

General reference

  • 1. Russo I, De Siena FP, Saponeri A, et al: Evaluation of anti-desmoglein-1 and anti-desmoglein-3 autoantibody titers in pemphigus patients at the time of the initial diagnosis and after clinical remission. Medicine (Baltimore) 96(46):e8801, 2017. doi: 10.1097/MD.0000000000008801

Symptoms and Signs of Pemphigus Foliaceus

The primary lesion is a flaccid vesicle or bulla, but due to the superficial location of the epidermal split, lesions tend to rupture, so intact bullae or vesicles are rarely evident on examination. Instead, well-demarcated, scattered, crusted, erythematous lesions are common on the face, scalp, and upper trunk. Mucosal involvement is rare. Skin lesions can burn and cause pain, but patients are typically not severely ill. Pemphigus erythematosus tends to affect the malar cheeks.

Diagnosis of Pemphigus Foliaceus

  • Skin biopsy and immunofluorescence

Diagnosis of pemphigus foliaceus is by biopsy of a lesion and adjacent (perilesional) unaffected skin that shows IgG autoantibodies against the keratinocyte cell surface via direct immunofluorescence. Autoantibodies to desmoglein 1 can be detected in serum via direct immunofluorescence, indirect immunofluorescence, and enzyme-linked immunosorbent assay (ELISA).

Treatment of Pemphigus Foliaceus

  • Corticosteroids, topical or systemic

If the disease is localized and not severe, high-potency topical corticosteroids are typically effective. More widespread or severe cases require systemic corticosteroids plus, at times, other immunosuppressive therapies, such as rituximab, plasma exchange, methotrexate, mycophenolate mofetil, or azathioprine. Topical calcineurin inhibitors have also been used.

Limited studies suggest that addition of a combination of tetracycline 500 mg orally 4 times a day or doxycycline 100 mg orally twice a day and nicotinamide 500 mg orally 3 times a day may be effective in some people.

Click here for Patient Education
NOTE: This is the Professional Version. CONSUMERS: Click here for the Consumer Version
Professionals also read
Test your knowledge
Pressure Injury
Pressure ulcers (PUs) are defined as areas of necrosis and ulceration where tissues are compressed between bone and hard surfaces, such as a bed or chair. There are many risk factors for PUs, which include age > 65 years, decreased mobility, and impaired sensation, among others. Of the main factors that influence the development of PUs, which of the following contributes to PUs but is not a direct cause?  
Download the Manuals App iOS ANDROID
Download the Manuals App iOS ANDROID
Download the Manuals App iOS ANDROID

Also of Interest