Pénfigo bulloso
Revisado por pares por Dr Rosalyn Adleman, MRCGPÚltima actualización por Dr Caroline Wiggins, MRCGP Last updated 25 de mayo de 2023
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En esta serie:Pénfigo vulgar
El pénfigo ampolloso es una enfermedad de la piel que puede causar sarpullido, picazón y ampollas. Afecta principalmente a personas mayores de 70 años. El tratamiento suele ser efectivo para controlar los síntomas. Generalmente se emplean cremas con esteroides o medicamentos, aunque en ocasiones pueden usarse otros medicamentos. La condición tiende a desaparecer después de 3-6 años y luego se puede suspender el tratamiento. A veces, la enfermedad persiste.
At a glance
Bullous pemphigoid is a rare skin condition causing an itchy rash and fluid-filled blisters.
The itch or rash can appear weeks or months before blisters.
It is an autoimmune disease where the immune system attacks the skin.
Certain conditions or medicines may trigger bullous pemphigoid.
Diagnosis involves a skin biopsy and a blood test.
Treatment for bullous pemphigoid mainly involves steroid creams or tablets.
The condition often resolves after 3 to 6 years, but can persist in some people.
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¿Qué es el penfigoide ampolloso?
Bullous pemphigoid is a skin condition that can cause a rash, itching and blisters.
There are several skin conditions which cause blisters. It is important to know exactly which disease you have as they have similar sounding names but vary greatly in their seriousness, outlook (prognosis) and treatment. For example, see the separate leaflet called Pemphigus Vulgaris (which is generally more serious than bullous pemphigoid).
Symptoms of bullous pemphigoid
Volver al contenidoSymptoms of bullous pemphigoid include:
Areas of itchy skin.
Pink rash which can look like eczema or urticaria.
Firm and dome-shaped fluid-filled blisters.
Small blisters inside the mouth or on the lips.
The itch or rash can develop weeks or months before the blisters appear.
Any area of skin can be affected, but blisters mostly occur on the arms, legs, armpits and groin. The amount of blistering can vary: sometimes it is just one area, such as the lower leg. In severe cases, the whole body may be affected.
This photo shows the typical blisters:
Ampollas en las piernas por penfigoide ampolloso

© Mohammad2018, CC BY-SA 4.0, a través de Wikimedia Commons
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How common is bullous pemphigoid?
Volver al contenidoBullous pemphigoid is rare. In the UK it is estimated that between 4-5 people in 100,000 develop it each year. Most people with bullous pemphigoid are aged over 70. It is very rare in children. It is not contagious so you cannot catch it from an affected person.
It can come on in pregnancy, when it is called gestational pemphigoid and requires careful management by a dermatologist and an obstetrician together.
What causes bullous pemphigoid?
Volver al contenidoBullous pemphigoid is an autoimmune disease. El sistema inmunológico normally makes antibodies to attack bacteria, viruses, and other germs. In people with bullous pemphigoid, the immune system makes antibodies against the basement membrane between the top layer of skin (the epidermis) and the next layer (the dermis). This causes fluid to build up as blisters between these two layers of skin.
It is not known what causes bullous pemphigoid. but certain conditions and medications may trigger it. They include:
Diseases which involve the nervous system such as dementia and multiple sclerosis.
Medications such as furosemida, medicamentos antiinflamatorios no esteroides (AINEs), captopril, some diabetes medicines and some antibiotic medicines.
Can stress cause bullous pemphigoid?
There is no evidence that stress causes or triggers this condition.
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How is bullous pemphigoid diagnosed?
Volver al contenidoThe diagnosis may take a while as it may look like eczema or an allergy at first. There are also several conditions which can cause blisters. If your doctor suspects that you have bullous pemphigoid, they will refer you to a skin specialist. Tests are usually done to confirm the diagnosis. These are:
A small sample (biopsy) of skin may be taken. This is looked at under the microscope and tested to confirm that the blisters are due to bullous pemphigoid.
Un análisis de sangre can detect the antibody that causes bullous pemphigoid (the bullous pemphigoid auto-antibody).
Tratamiento del penfigoide ampolloso
Volver al contenidoTreatment aims to improve your symptoms and avoid side effects.
Treatments used for bullous pemphigoid are:
Esteroides
Steroids are the main treatment for bullous pemphigoid.
High-strength steroid creams, also called topical steroids (for example, clobetasol) will normally be needed.
Steroid tablets such as prednisolona are commonly used with or without steroid creams, especially if the rash is on more than one body area, or there are practical problems applying the cream. Steroids reduce inflammation and suppress the immune system.
Side-effects
All steroids can have side-effects. Side-effects from steroids can be serious, especially if you take high doses for a long time.
If you take steroid treatment for more than a month, you will usually be advised to take additional medications to reduce the risk of serious side effects. It is important not to stop steroids without discussing it with your doctor first. For more information see the separate leaflet called Oral Steroids.
Other drugs to calm the immune system may be used if you cannot use steroids or they are not working to control your condition.
Looking after your skin is important with this condition, and you may be advised to use certain creams or moisturisers to wash with, or apply to your skin to keep it in the best condition possible.
What is the outlook for bullous pemphigoid?
Volver al contenidoBullous pemphigoid usually goes away after 3-6 years. Treatment can then be stopped. In some people the condition unfortunately persists.
Widespread or severe bullous pemphigoid is a serious condition. In addition to the side effects caused by the treatments, it can be fatal due to the risk of broken areas of skin developing a bacterial infection.
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Preguntas frecuentes
Can children get bullous pemphigoid?
Bullous pemphigoid is very rare in children. It primarily affects people aged over 70.
If I have bullous pemphigoid, can I pass it on to someone else?
No, bullous pemphigoid is not contagious. You cannot catch it from an affected person.
Is bullous pemphigoid related to other conditions that cause blisters?
There are several skin conditions that cause blisters. It is important to get an exact diagnosis as they can have similar-sounding names but vary greatly in their seriousness, outlook, and treatment. For example, pemphigus vulgaris is generally more serious than bullous pemphigoid.
How long does it take for bullous pemphigoid to clear up?
Bullous pemphigoid usually resolves after 3-6 years, at which point treatment can often be stopped. However, in some individuals, the condition unfortunately persists for longer.
Are there any risks associated with bullous pemphigoid?
Widespread or severe bullous pemphigoid can be a serious condition. There is a risk of broken areas of skin developing a bacterial infection, which can be fatal. Additionally, the treatments themselves, especially steroids, can have serious side-effects, particularly with high doses or long-term use.
What is the typical appearance of the blisters in bullous pemphigoid?
The blisters in bullous pemphigoid are typically firm, fluid-filled, and dome-shaped. They can appear on any area of skin, but are most common on the arms, legs, armpits, and groin. Small blisters may also occur inside the mouth or on the lips.
What should I do if I am pregnant and develop symptoms of blistering?
If you are pregnant and develop bullous pemphigoid, known as gestational pemphigoid, it requires careful management by both a dermatologist and an obstetrician together.
Lecturas adicionales y referencias
- Guías para el manejo del penfigoide ampolloso; Asociación Británica de Dermatólogos (2012)
- Di Lernia V, Casanova DM, Goldust M, et al; Pénfigo Vulgar y Penfigoide Ampolloso: Actualización sobre Diagnóstico y Tratamiento. Dermatol Pract Concept. 29 de junio de 2020;10(3):e2020050. doi: 10.5826/dpc.1003a50. eCollection julio de 2020.
- DermnetNZ Bullous Pemphigoid
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About the authorView full bio

Dr Caroline Wiggins, MRCGP
Médico General, Autor Médico
MBBS Honores (con Distinción), MRCGP (2016), MSc.SEM (con Distinción), BSc (Hons)
Dr Caroline Wiggins is a GP locum currently in the South-West of England.
About the reviewerView full bio

Dr Rosalyn Adleman, MRCGP
MRCGP
Dr Rosalyn Adleman, is an NHS GP working in north London.
Historial del artículo
La información en esta página está escrita y revisada por pares por clínicos calificados.
Siguiente revisión prevista: 23 de mayo de 2028
25 de mayo de 2023 | Última versión

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