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Lichen planus pemphigoides after COVID‐19 infection.

Authors :
Didona, D.
Sequeira‐Santos, Antonio M.
Hinterseher, J.
Cunha, T.
Hertl, M.
Source :
Journal of the European Academy of Dermatology & Venereology; Feb2024, Vol. 38 Issue 2, pe131-e133, 3p
Publication Year :
2024

Abstract

This article discusses a rare autoimmune bullous disease called lichen planus pemphigoides (LPP) that developed in a 50-year-old Caucasian male two weeks after a COVID-19 infection. LPP is characterized by lichenoid and/or bullous skin lesions and the presence of IgG autoantibodies against certain proteins in the skin and mucous membranes. The patient in this case study exhibited the clinical, histopathological, and serological criteria for LPP. The article also mentions the overlap between LPP, bullous lichen planus, and bullous pemphigoid, and highlights the importance of detecting autoantibodies to support the diagnosis. This is the first reported case of LPP after a COVID-19 infection. [Extracted from the article]

Details

Language :
English
ISSN :
09269959
Volume :
38
Issue :
2
Database :
Complementary Index
Journal :
Journal of the European Academy of Dermatology & Venereology
Publication Type :
Academic Journal
Accession number :
175055025
Full Text :
https://doi.org/10.1111/jdv.19542