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Case Report: A rare co-occurrence of IgA pemphigus and pyoderma gangrenosum associated with IgA-κ type monoclonal gammopathy of undetermined significance: a 19-year diagnostic and therapeutic journey

We report a complex case of neutrophilic dermatosis (ND) in a 61-year-old woman with a 19-year history of recurrent, pruritic, and painful vesiculopustular eruptions. Her clinical course was marked by evolving diagnoses, from pustular vasculitis to IgA pemphigus and pyoderma gangrenosum (PG). Concur...

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Principais autores: You Xie, Xinqiao Liu, Juan Wu, Liuqing Chen, Jinbo Chen
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2026-05-01
coleção:Frontiers in Immunology
Assuntos:
dapsone
IgA pemphigus
monoclonal gammopathy
neutrophilic dermatosis
pyoderma gangrenosum
Acesso em linha:https://www.frontiersin.org/articles/10.3389/fimmu.2026.1832860/full
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