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Clinical Journal of Gastroenterology

, Volume 12, Issue 1, pp 25–28 | Cite as

Oesophageal pemphigoid: a rare cause of dysphagia

  • Michael McFarlaneEmail author
  • Ayesha Azam
  • David Snead
  • Ben Disney
Case Report
  • 69 Downloads

Abstract

Pemphigus vulgaris (PV) is a rare autoimmune bullous disease which affects the skin and mucous membranes. Oesophageal involvement is rare and has previously been limited to case reports and case series. A recent large case series of 477 PV patients showed that 26/477 (5.4%) had symptomatic oesophageal involvement. We present the case of a 54-year-old Somalian lady with a 10-year history of cutaneous PV, currently in remission, who developed dysphagia and odynophagia and was subsequently found to have oesophageal PV involvement with multiple flaccid bullae which were positive for anti-DSG3 antibodies on in-direct immunofluorescence. She had her treatment switched from azathioprine to mycophenolate and prednisolone, leading to resolution of her symptoms.

Keywords

Pemphigus vulgaris Oesophageal Dysphagia 

Notes

Compliance with ethical standards

Conflict of interest

M.McFarlane, A. Azam, D. Snead and B. Disney declare that they have no conflicts of interest.

Human rights

All procedures followed have been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments.

Informed consent

Informed consent was obtained from all patients for being included in the study.

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Copyright information

© Japanese Society of Gastroenterology 2018

Authors and Affiliations

  1. 1.Department of GastroenterologyUHCWCoventryUK
  2. 2.Department of HistopathologyUHCWCoventryUK

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