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.

Xie Y, Liu X, Wu J, Chen L, Chen J

Open source

DOI
10.3389/fimmu.2026.1832860
Published
2026
Container
Frontiers in immunology
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.3389/fimmu.2026.1832860,
  title = {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.},
  author = {Xie Y and Liu X and Wu J and Chen L and Chen J},
  year = {2026},
  journal = {Frontiers in immunology},
  doi = {10.3389/fimmu.2026.1832860},
  url = {https://doi.org/10.3389/fimmu.2026.1832860}
}

RIS

TY  - JOUR
TI  - 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.
AU  - Xie Y
AU  - Liu X
AU  - Wu J
AU  - Chen L
AU  - Chen J
PY  - 2026
JO  - Frontiers in immunology
DO  - 10.3389/fimmu.2026.1832860
UR  - https://doi.org/10.3389/fimmu.2026.1832860
ER  - 

APA

Y, X., X, L., J, W., L, C., & J, C. (2026). 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.. Frontiers in immunology. https://doi.org/10.3389/fimmu.2026.1832860

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