References

Carey B, Setterfield J. Mucous membrane pemphigoid and oral blistering diseases. Clin Exp Dermatol. 2019; 44:732-739
Kanjanabuch P, Arporniem S, Thamrat S, Thumasombut P. Mucous membrane pemphigoid in a patient with hypertension treated with atenolol: a case report. J Med Case Rep. 2012; 6
Gaudin O, Seta V, Alexandre M Gliptin accountability in mucous membrane pemphigoid induction in 24 out of 313 patients. Front Immunol. 2018; 9
Porcelli B, Pozza A, Bizzaro N Association between stressful life events and autoimmune diseases: a systematic review and meta-analysis of retrospective case-control studies. Autoimmun Rev. 2016; 15:325-334
Stojanovich L, Marisavljevich D. Stress as a trigger of autoimmune disease. Autoimmun Rev. 2008; 7:209-213
Setterfield J, Shirlaw P, Kerr-Muir M Mucous membrane pemphigoid: a dual circulating antibody response with IgG and IgA signifies a more severe and persistent disease. Br J Dermatol. 1998; 138:602-610
Yancey KB, Egan CA. Pemphigoid: clinical, histologic, immunopathologic, and therapeutic considerations. JAMA. 2000; 284:350-356
Mihai S, Sitaru C. Immunopathology and molecular diagnosis of autoimmune bullous diseases. J Cell Mol Med. 2007; 11:462-481
Zillikens D. Diagnosis of autoimmune bullous skin diseases. Clin Lab. 2008; 54:491-503
Carey B, Joshi S, Abdelghani A The optimal oral biopsy site for diagnosis of mucous membrane pemphigoid and pemphigus vulgaris. Br J Dermatol. 2020; 182:747-753
Giurdanella F, Diercks GF, Jonkman MF Laboratory diagnosis of pemphigus: direct immunofluorescence remains the gold standard. Br J Dermatol. 2016; 175:185-186
Schmidt E, Zillikens D. Pemphigoid diseases. Lancet. 2013; 381:320-332
Taylor J, McMillar R, Shephard M World Workshop on Oral Medicine VI: a systematic review of the treatment of mucous membrane pemphigoid. Oral Surg Oral Med Oral Pathol Oral Radiol. 2015; 120:161-171
Mays JW, Carey BP, Posey R World Workshop of Oral Medicine VII: a systematic review of immunobiological therapy for oral manifestations of pemphigoid and pemphigus. Oral Dis. 2019; 25:(1)111-121

Stressful Life Events as a Trigger for Autoimmune Disease? A Case Report on Mucous Membrane Pemphigoid

From Volume 48, Issue 5, May 2021 | Pages 379-382

Authors

Robert Devine

BDS (QMUL), MJDF

Dental Core Trainee in Oral and Maxillofacial Surgery, Royal United Hospitals, Bath

Articles by Robert Devine

Email Robert Devine

Melanie Simms

BDS, MFDS RCPS(Glasg), PGCert (Dent Ed)

StR Oral Medicine, University Dental Hospital, Cardiff

Articles by Melanie Simms

Abstract

This case discusses the acute presentation of a patient with mucous membrane pemphigoid to an emergency dental department. Mucous membrane pemphigoid is a rare condition, but its presentation can be severe and concerning for both the patient and clinician. The case presents the manifestations of florid desquamative gingivitis and extensive mucosal erosions due to burst bullae. We discuss the possible causes of the condition in this patient, likely to be the stress of recent cardiac surgery, as well as exploring the efficacy of diagnostic tools, treatment options and adverse effects of corticosteroid treatment.

CPD/Clinical Relevance: Correct and timely diagnosis of vesiculobullous disorders has notable impacts on patient outcomes and quality of life.

Article

Mucous membrane pemphigoid (MMP) is a rare subepithelial bullous disorder predominantly involving the oral mucosa. Other mucous membranes that may be affected include the upper part of the aerodigestive tract, conjunctiva and genital mucosa. Occasionally the skin may also be involved.1 There is an inflammatory autoimmune response directed against the hemidesmosome adhesion complex, leading to subepithelial clefting and the clinical appearance of desquamative gingivitis, blisters or erosions. This case presents an acute presentation of MMP as florid desquamative gingivitis and extensive mucosal erosions. This article explores the efficacy of diagnostic tools available to identify the condition, discusses the immediate, short- and long-term treatment modalities as well as hypothesizes potential initiating stressor events and response to therapy.

A 64-year-old male presented to the dental emergency department at the University Hospital, Wales, complaining of painful, ‘peeling’ and bleeding gums. He found that brushing his teeth made the gums develop blood-filled blisters, prior to bursting and leaving a painful ulcerated area that did not heal. The patient reported one single episode of a blister on the skin of his nose that had since healed, and reported no other cutaneous, genital or ocular symptoms.

Register now to continue reading

Thank you for visiting Dental Update and reading some of our resources. To read more, please register today. You’ll enjoy the following great benefits:

What's included

  • Up to 2 free articles per month
  • New content available