Pemphigus vulgaris
Pemphigus vulgaris (PV) is an autoimmune disorder of the skin. It involves blistering and sores (erosions) of the skin and mucous membranes.
Pemphigus vulgaris is an autoimmine disorder, where the body's immune system attacks some of the proteins in the skin. Pemphigus usually occurs in middle-aged or older people. This picture shows a close-up of the blistering on the back. Most of the blisters have broken (denuded), which is common since these blisters are fragile.
Pemphigus vulgaris is an autoimmine disorder, where the body's immune system attacks some of the proteins in the skin. Pemphigus usually occurs in middle-aged or older people. This picture shows a close-up of lesions in the mouth.
Causes
The immune system produces antibodies against specific proteins in the skin and mucous membranes. These antibodies break the bonds between skin cells. This leads to the formation of a blister. The exact cause is unknown.
In rare cases, PV is caused by some medicines, including:
- A medicine called penicillamine, which removes certain materials from the blood (chelating agent)
- Blood pressure medicines called ACE inhibitors
- Nonsteroidal anti-inflammatory drugs (NSAIDs)
PV is uncommon. It most often occurs in middle-aged or older people.
Symptoms
About 50% of people with this condition first develop painful blisters and sores in the mouth. This is followed by skin blisters. Skin sores may come and go.
The skin sores may be described as:
- Draining
- Oozing
- Crusting
- Peeling or easily detached
They may be located:
- In the mouth and down the throat
- On the scalp, trunk, or other skin areas
Exams and Tests
The skin separates easily when the surface of unaffected skin is rubbed sideways with a cotton swab or finger. This is called a positive Nikolsky sign.
A skin biopsy and blood tests are often done to confirm the diagnosis.
Treatment
Severe cases of PV may need wound management, similar to the treatment for severe burns. People with PV may need to stay in a hospital and receive care in a burn unit or intensive care unit.
Treatment is aimed at reducing symptoms, including pain. It also aims to prevent complications, especially infections.
Treatment may involve:
- Antibiotics and antifungal medicines to control or prevent infections
- Fluids and electrolytes given through a vein (IV) if there are severe mouth ulcers
- IV feedings if there are severe mouth ulcers
- Numbing (anesthetic) mouth lozenges to reduce mouth ulcer pain
- Pain medicines if local pain relief is not enough
Body-wide (systemic) therapy is needed to control PV and should be started as early as possible. Systemic treatment includes:
- An anti-inflammatory medicine called dapsone
- Corticosteroids
- Medicines containing gold
- Medicines that suppress the immune system (such as azathioprine, methotrexate, cyclosporine, cyclophosphamide, mycophenolate mofetil, or rituximab)
Antibiotics may be used to treat or prevent infection. Intravenous immunoglobulin (IVIg) is occasionally used.
Plasmapheresis may be used along with systemic medicines to reduce the amount of antibodies in the blood. Plasmapheresis is a process in which antibody-containing plasma is removed from the blood and replaced with intravenous fluids or donated plasma.
Ulcer and blister treatments include soothing or drying lotions, wet dressings, or similar measures.
Outlook (Prognosis)
Without treatment, this condition can be life threatening. Severe infection is the most frequent cause of death.
With treatment, the disorder tends to be chronic. Side effects of treatment may be severe or disabling.
Possible Complications
Complications of PV include:
- Secondary skin infections
- Severe dehydration
- Side effects of medicines
- Spread of infection through the bloodstream (sepsis)
When to Contact a Medical Professional
Your health care provider should examine any unexplained blisters.
Contact your provider if you have been treated for PV and you develop any of the following symptoms:
- Chills
- Fever
- General ill feeling
- Joint aches
- Muscle aches
- New blisters or ulcers
References
Amagai M. Pemphigus. In: Bolognia JL, Schaffer JV, Cerroni L, eds. Dermatology. 5th ed. Philadelphia, PA: Elsevier; 2025:chap 29.
Dinulos JGH. Vesicular and bullous diseases. In: Dinulos JGH, ed. Habif's Clinical Dermatology. 7th ed. Philadelphia, PA: Elsevier; 2021:chap 16.
James WD, Elston DM, Treat JR, Rosenbach MA, Neuhaus IM. Chronic blistering dermatoses. In: James WD, Elston DM, Treat JR, Rosenbach MA, Neuhaus IM, eds. Andrew's Diseases of the Skin. 13th ed. Philadelphia, PA: Elsevier; 2020:chap 21.
Patterson JW. The vesiculobullous reaction pattern. In: Patterson JW, ed. Weedon's Skin Pathology. 5th ed. Philadelphia, PA: Elsevier; 2021:chap 7.
Version Info
Last reviewed on: 5/28/2024
Reviewed by: Ramin Fathi, MD, FAAD, Director, Phoenix Surgical Dermatology Group, Phoenix, AZ. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.
