| Literature DB >> 30141184 |
Michael McFarlane1, Ayesha Azam2, David Snead2, Ben Disney3.
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.Entities:
Keywords: Dysphagia; Oesophageal; Pemphigus vulgaris
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Year: 2018 PMID: 30141184 DOI: 10.1007/s12328-018-0897-6
Source DB: PubMed Journal: Clin J Gastroenterol ISSN: 1865-7265