King's College London

Research portal

Mucous membrane pemphigoid and oral blistering diseases

Research output: Contribution to journalReview article

Original languageEnglish
Pages (from-to)732-739
Number of pages8
JournalClinical and Experimental Dermatology
Volume44
Issue number7
Early online date18 May 2019
DOIs
Publication statusPublished - 1 Oct 2019

King's Authors

Abstract

The autoimmune blistering disorders present with variable frequency in the oral cavity. Recognition of their key clinical features at presentation is important as there are many causes of oral ulceration. Careful history-taking, clinical examination, an understanding of pathogenesis and appropriate investigations are essential.
With the exception of the rare genodermatoses that may lead to blistering and oral ulceration, the majority of patients have an acquired disorder. These include the rare autoimmune blistering diseases mucous membrane pemphigoid (MMP), pemphigus vulgaris (PV), linear IgA disease (LAD), epidermolysis bullosa acquisita (EBA) and paraneoplastic pemphigus (PNP). Important clinical differential diagnoses include erythema multiforme (EM) which may be mistaken for PV in appearance while oral lichen planus (LP) may be indistinguishable from MMP. Angina bullosa haemorrhagica (ABH) may also present with tense haemorrhagic bullae and in the absence of diagnostic tests, requires an astute clinical diagnosis based upon the history.
Newer laboratory techniques have facilitated identification of target antigens and epitopes in the autoimmune blistering diseases particularly in MMP. Current interest is in whether these relate to clinical presentation and outcomes. There has also been recent investigation in to the use of saliva as an alternative medium to serum for the diagnosis of oral vesiculobullous lesions.
Assessment of disease severity and measurement of QOL at presentation and at subsequent follow up, is paramount to interpreting therapeutic response. Furthermore, combining these scores with serological and/or salivary biomarkers is valuable in the assessment of clinical response. Here we discuss mucous membrane pemphigoid (MMP) and its important differential diagnoses.

View graph of relations

© 2018 King's College London | Strand | London WC2R 2LS | England | United Kingdom | Tel +44 (0)20 7836 5454