| Literature DB >> 32641304 |
Eliana Carolina Morel-Cerda1, Bryan Adrian Priego-Parra1, Peter Grube-Pagola1, Jose Maria Remes-Troche2.
Abstract
Pemphigus is a rare autoimmune disease that causes blistering of the skin and oral mucosa. In bullous pemphigoid (BP), skin involvement is predominant, whereas oesophageal involvement is rare, compared with other blistering diseases. We present, herein, the case of a 67-year-old man with a history of successfully treated BP that 2 years later developed progressive dysphagia, unintentional weight loss and iron deficiency anaemia. An endoscopy with biopsies was performed, and its findings were consistent with 'sloughing esophagitis' (esophagitis dissecans superficialis) associated with BP. Oesophageal involvement was present during the first weeks, making our case unusual due to the isolated oesophageal symptoms that developed 24 months later. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: endoscopy; oesophagus; pathology; skin
Mesh:
Year: 2020 PMID: 32641304 PMCID: PMC7348641 DOI: 10.1136/bcr-2020-235135
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X