| Literature DB >> 31147410 |
Fatima Awdeh1, Eimear Gilhooley1, Ciara O Grady1, Maureen Connolly1.
Abstract
Autoimmune blistering diseases are rare but potentially life-threatening conditions. Pemphigus foliaceus is one of these conditions, characterised by superficial erosions of the skin without mucosal involvement. We report the case of a 57-year-old woman who presented with a 4-week history of rash affecting her scalp with associated hair loss. Clinical and histopathological findings were in keeping with pemphigus foliaceus. She was successfully treated with rituximab, a chimeric monoclonal antibody against CD20, leading to a transient depletion of B cells. After 5 months of follow-up, her rash had cleared, and her hair had completely regrown. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: dermatology; pathology
Mesh:
Substances:
Year: 2019 PMID: 31147410 PMCID: PMC6557388 DOI: 10.1136/bcr-2018-229026
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X