Bullous Pemphigoid

oPatientPlus articles are written by UK doctors and are based on research evidence, UK and European Guidelines. They are designed for health professionals to use, so you may find the language more technical than the condition leaflets.

Bullous pemphigoid (BP) is a chronic, autoimmune, subepidermal, blistering skin disorder (unlike pemphigus where the blistering is intra-epidermal). Clear diagnostic criteria can be lacking for definitive diagnosis in less than clear-cut cases.[1]

The autoantigen is type XVII collagen (COL17), also called BP180 or BPAG2, a protein that forms the junction between the epidermis and the basement membrane of the dermis.[2] Direct immunofluorescence (DIF) studies of the blister skin show deposition of IgG and complement (C3) at the dermal/epidermal junction. Analysis of this skin when split, shows deposition of IgG on the epidermis half (the roof), rather than the dermal side, the floor, of the blister. This feature distinguishes bullous pemphigoid (BP) from other autoimmune blistering skin diseases.

CD4-positive T cells are thought to play a major role in the development of BP.

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  • The incidence of pemphigoid in the UK is estimated at 4.3 per 100,000 persons per year.[3]  In other parts of Europe the incidence is 0.7-1.3 per 100,000.
  • It is the most commonly seen autoimmune blistering disease in the West.
  • Pemphigoid can affect individuals of any age, but mean age of onset is 80 years.
  • Males and females are equally affected.

It is important to ask about past medical history and medication, as this may reveal conditions associated with bullous pemphigoid (BP).

  • Past medical history:
    • BP may follow any chronic inflammatory skin disease, even those not normally associated with blisters.
    • Lichen planus and psoriasis may precede the development of BP.
  • Medication may be associated with onset of BP:
    • Furosemide
    • Non-steroidal anti-inflammatory drugs
    • Captopril
    • Penicillamine
    • Antibiotics
  • Other triggers:
    • Ultraviolet irradiation
    • Radiotherapy[4]

The initial presentation of pemphigoid is very variable, as blistering skin lesions may only occur late in the course of the disease. Symptoms and signs may present with a subacute or acute onset. Symptoms and signs which may be seen in patients with all forms of bullous pemphigoid (BP) include:

  • Itch, or pruritus, which is frequently a feature. This may occur weeks or months before the appearance of any visible skin lesion.
  • Rash. An urticarial or erythematous rash may precede the appearance of the blisters.
  • Blisters or bullae, which are typical and often occur in skin flexures. Depending on the form of BP these may affect a single site or be more widespread.
  • Mucous membranes. BP involves the mucosa in up to a quarter of patients. The blisters appear mainly on palatal mucosa. They may be clinically insignificant but can cause problems with dysphagia.

Different clinical forms

There are several distinct clinical presentations.

  • Generalised bullous is the most common form:
    • Tense bullae can form anywhere but commonly around flexural areas. They can appear both on normal and erythematous skin.
    • Mucosal involvement is rare and not clinically significant when it does occur.
    • The bullae heal without scarring.
    BULLOUS PEMPHIGOID
  • Vesicular is a less common form:
    • It presents typically with small groups of tense blisters which collect on erythematous areas of skin (rather than normal skin).

Other rarer forms include vegetative, generalised erythroderma, urticarial, nodular (or pemphigoid nodularis) and acral (a childhood form associated with vaccination[5]).

The differential diagnoses will include:[6]

Other conditions which may be considered include:

  • Other blistering skin disorders such as chickenpox.
  • Impetigo, which may be mistaken for the various stages of bullous pemphigoid (BP).
  • Urticaria.
  • The bullous eruption of systemic lupus erythematosus.
  • Herpes gestationis or gestational pemphigoid. This presents in the late second or third trimester, and resolves on delivery. It is immunologically identical to BP.

Skin biopsy followed by direct immunofluorescence (DIF) is the investigation most commonly used to make the diagnosis. Indirect immunofluorescence (IDIF) using fluid aspirated from the blister, may also be used.

  • DIF studies.[8] DIF demonstrates IgG in up to 90% of patients and C3 deposition in nearly 100% of patients. DIF can differentiate bullous pemphigoid (BP) from cicatricial pemphigoid and epidermolysis bullosa acquisita by incubating the skin biopsy sample in a salt solution before DIF.
  • The best skin samples for diagnosis come from apparently normal skin near a BP lesion.[3]  Fresh specimens are best, as transport media may give false negative results.
  • Histological tests. These reveal a subepidermal blister with inflammatory infiltrate and usually eosinophilic predominance.

There are other experimental procedures.

  • Direct and indirect immunoelectron microscopy.
  • Immunoblotting.[9]
  • Immunoprecipitation.
  • Enzyme-linked immunosorbent assay.

It had been thought that bullous pemphigoid (BP) may be associated with the presence of malignant tumours; however, age- and sex-matched studies have concluded that no such association exists.[10]

General points

  • One of the main aims is to reduce blister formation with the minimum dose of medication necessary.[11]
  • All therapeutic regimes should be tailored to the individual and any pre-existing conditions.
  • This is particularly true for elderly patients where the use of aggressive treatment regimes may put the patient more at risk than the disease itself.
  • As the disease may last some considerable time, all patients should be monitored until they are off all treatment and are in complete remission.

Medication

Recommendations have been made by the British Association of Dermatologists for the treatment of bullous pemphigoid (BP).[3]  These have been supplemented with information and advice from more recent papers and reviews:

  • Strong topical corticosteroid treatment (clobetasol) is good as first-line in localised disease. It is safe and effective but its use in extensive disease may be limited by side-effects and practical factors.[12] Topical is better tolerated than oral steroids, particularly in the elderly.[13]
  • For more severe cases, systemic steroids along with immunosuppressives may be needed to control the disease.[14] Doses varying from 0.75-1.0mg/kg per day are used. The dose varies with the severity of the disease. Treatment to help prevent osteoporosis (calcium and vitamin D supplements, bisphosphonates) should be initiated if the systemic steroid will be given for more than one month.
  • The effectiveness of adding plasma exchange or azathioprine to corticosteroids, and combination treatment with tetracycline and nicotinamide has not yet been adequately established.[12]

Oral steroid is effective in 60-90% of patients within 1-4 weeks.[3]  Attempts to withdraw treatment should be made at 2-4 weekly intervals. Most patients need treatment for between 6 months to 4 years. Many have long-term remission of the disease afterwards.

Potential therapies

Several other therapies have been studied with respect to their usefulness in the treatment of BP:

  • Dapsone and sulphonamides: there is some evidence to suggest that dapsone and the sulphonamides might have an effect on BP.[15] However, their side-effect profile is not encouraging, and these treatments should be reserved for those patients in whom other agents have been ineffective or are contra-indicated.
  • Rituximab may be useful in difficult-to-treat cases.[16][17]
  • Secondary infections.
  • Immunosuppression.
  • Corticosteroid side-effects (hypertension, diabetes, osteoporosis, heart disease).
  • Bullous pemphigoid (BP) is a chronic inflammatory disease which can persist with remissions and exacerbations for months or years.
  • It is normally self-limiting and remits within five years . If treated, BP will remit within 1.5 to 5 years.[6]
  • With optimal therapy, the mortality rate today is in the order of 6-41%, the vast majority of deaths occurring in elderly patients with co-existing disease.
  • Elderly patients are also particularly at risk from the immunosuppressive effects of therapy, which may place them at greater risk of life-threatening events than the disease itself.
  • A recent analysis of mortality statistics from bullous skin disorders (between 1979 and 2002) in the USA showed little change in mortality rates for BP.[18] This differs from findings in the UK.[19]
  • Patients on corticosteroids and immunosuppressants are, for example, at risk of peptic ulcer disease, agranulocytosis and diabetes.

Further reading & references

  1. Lipsker D, Borradori L; 'Bullous' pemphigoid: what are you? Urgent need of definitions and diagnostic Dermatology. 2010;221(2):131-4. Epub 2010 Jul 30.
  2. Wong HK, Bechtel MA; Blistering insights into the pathogenesis of bullous pemphigoid. Clin Immunol. 2011 Dec 13.
  3. Guidelines for the management of bullous pemphigoid, British Association of Dermatologists (2012)
  4. Mul VE, Verschueren TA, van Geest AJ, et al; Bullous pemphigoid (BP) induced by radiotherapy. Radiother Oncol. 2007 Jan;82(1):105. Epub 2006 Dec 11.
  5. Baykal C, Okan G, Sarica R; Childhood bullous pemphigoid developed after the first vaccination. J Am Acad Dermatol. 2001 Feb;44(2 Suppl):348-50.
  6. Chan LS et al: Bullous Pemphigoid, Medscape, Apr 2013
  7. Hofmann SC, Bruckner-Tuderman L; Bullous pemphigoid: diagnostics and new therapeutic strategies. Dtsch Med Wochenschr. 2006 Feb 24;131(8):389-92.
  8. Schmidt E, della Torre R, Borradori L; Clinical features and practical diagnosis of bullous pemphigoid. Dermatol Clin. 2011 Jul;29(3):427-38, viii-ix.
  9. Grootenboer-Mignot S, Descamps V, Picard-Dahan C, et al; Place of human amniotic membrane immunoblotting in the diagnosis of autoimmune Br J Dermatol. 2009 Nov 3.
  10. Jedlickova H, Hlubinka M, Pavlik T, et al; Bullous pemphigoid and internal diseases - A case-control study. Eur J Dermatol. 2009 Oct 2.
  11. Patton T, Korman NJ; Bullous pemphigoid treatment review. Expert Opin Pharmacother. 2006 Dec;7(17):2403-11.
  12. Kirtschig G, Middleton P, Bennett C, et al; Interventions for bullous pemphigoid. Cochrane Database Syst Rev. 2010 Oct 6;(10):CD002292.
  13. Fontaine J, Joly P, Roujeau JC; Treatment of bullous pemphigoid. J Dermatol. 2003 Feb;30(2):83-90.
  14. Welsh B; Blistering skin conditions. Aust Fam Physician. 2009 Jul;38(7):484-90.
  15. Gurcan HM, Ahmed AR; Efficacy of dapsone in the treatment of pemphigus and pemphigoid: analysis of Am J Clin Dermatol. 2009;10(6):383-96. doi: 10.2165/11310740-000000000-00000.
  16. Hertl M, Bernard P, Borradori L; Rituximab for severe mucous membrane pemphigoid: safe enough to be drug of first Arch Dermatol. 2011 Jul;147(7):855-6.
  17. Kasperkiewicz M, Shimanovich I, Ludwig RJ, et al; Rituximab for treatment-refractory pemphigus and pemphigoid: a case series of 17 J Am Acad Dermatol. 2011 Sep;65(3):552-8.
  18. Risser J, Lewis K, Weinstock MA; Mortality of bullous skin disorders from 1979 through 2002 in the United States. Arch Dermatol. 2009 Sep;145(9):1005-8.
  19. Langan SM, Smeeth L, Hubbard R, et al; Bullous pemphigoid and pemphigus vulgaris--incidence and mortality in the UK: BMJ. 2008 Jul 9;337:a180. doi: 10.1136/bmj.a180.

Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. EMIS has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.

Original Author:
Dr Richard Draper
Current Version:
Peer Reviewer:
Prof Cathy Jackson
Document ID:
2590 (v28)
Last Checked:
14/03/2012
Next Review:
13/03/2017