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Bullous pemphigoid
Other Resources UpToDate PubMed

Bullous pemphigoid

Contributors: Erin X. Wei MD, Jeffrey M. Cohen MD, Belinda Tan MD, PhD, Susan Burgin MD
Other Resources UpToDate PubMed


This summary discusses bullous pemphigoid in adult patients. Bullous pemphigoid of childhood is addressed separately.

Bullous pemphigoid (BP) is an autoimmune subepidermal blistering disease with average onset at around 60 years of age. There is no ethnic or sex predilection.

Pathogenesis includes development of autoantibodies against hemidesmosome adhesion complex in the basement membrane of the skin (BP180 and/or BP230), resulting in complement activation, mast cell degranulation, release of inflammatory mediators, and recruitment of neutrophils and eosinophils. This leads to the formation of localized or generalized urticarial plaques, erythematous papules or plaques, and/or bullae. The disease can occur on any body surface, but mucous membrane involvement is seen in only 10%-30% of patients.

BP has variable clinical presentation as well as disease course. Presentation can range from itch without rash to localized or generalized eruptions. The morphology may be variable: some presentations are nonbullous, in which case urticarial or eczematous-appearing papules and plaques, or excoriations only, may be seen. The localized variant can mimic dyshidrosis when on the palms or soles and can develop in sites of radiation, surgery, prior photodynamic therapy, infection, paralysis, and venous stasis, as well as adjacent to ostomies. Disease course ranges from self-limiting to chronic over months to years.

Peripheral eosinophilia can be seen in approximately 50% of patients and is positively correlated with disease severity. Its presence has also been correlated with older age and palmoplantar involvement. Lack of peripheral eosinophilia has been positively correlated with younger age and mucosal disease.

BP is associated with neurologic disease ranging from stroke to dementia. Relapse of BP has been shown to be more likely in individuals with extensive disease and dementia. BP is also been associated with other autoimmune diseases such as diabetes mellitus, thyroiditis, dermatomyositis, systemic lupus erythematosus, rheumatoid arthritis, ulcerative colitis, myasthenia gravis, and multiple sclerosis in case reports and case series. A population-based study from Finland strongly suggests an increased risk of BP in patients with dermatitis herpetiformis. Medications (ie, furosemide, NSAIDs, captopril, penicillamine, gliptins, PD-1 and PDL-1 inhibitors, and some antibiotics) have also been associated with triggering BP.


L12.0 – Bullous pemphigoid

77090002 – Bullous pemphigoid

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Last Reviewed:11/12/2020
Last Updated:06/04/2023
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Patient Information for Bullous pemphigoid
Contributors: Taylor Williams, Chase W. Kwon MD
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Bullous pemphigoid
A medical illustration showing key findings of Bullous pemphigoid : Tense bullae, Pruritus, Tense vesicles, Excoriations, Peripheral eosinophilia
Clinical image of Bullous pemphigoid - imageId=108986. Click to open in gallery.  caption: 'A close-up of a tense bulla and a vesicle at the edge of a healing eroded plaque.'
A close-up of a tense bulla and a vesicle at the edge of a healing eroded plaque.
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