Article
IgG4-RD-Associated Mikulicz Syndrome Without Classic Systemic Involvement<span style="mso-ansi-language: ES-MX;">
2025-01-29
Abstract excerpt
<h4>Background: </h4> IgG4-related disease is a rare, chronic inflammatory disorder characterized by lymphoplasmacytic infiltration, ‘storiform’ fibrosis, and elevated IgG4 levels in affected tissues. This disease has a broad and heterogeneous clinical spectrum that includes four main phenotypes: pancreatic-hepatobiliary disease, retroperitoneal/aortic fibrosis, head and neck disease, and Mikulicz synd...
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Identifiers and source
- Literature Corpus work
- 0a62f46f-9ccf-5bc8-9030-178962d588f1
- DOI
- 10.20944/preprints202501.2109.v1