A case of IgA pemphigus with acantholysis in oral mucosal lesions
Abstract IgA pemphigus is an autoimmune bullous disease caused by anti‐keratinocyte cell surface IgA autoantibodies. Mucous membrane involvement is rare in IgA pemphigus. We report a case of IgA pemphigus with oral mucosal lesions, in which acantholysis was pathologically confirmed. A 31‐year‐old wo...
| Main Authors: | , , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wiley
2024-04-01
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| Series: | Skin Health and Disease |
| Online Access: | https://doi.org/10.1002/ski2.327 |