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- W2567103616 abstract "IgG4-related disease (IgG4-RD) is a multiorgan immune-mediated condition that mimics many malignant, infectious, and inflammatory disorders (1–3). The diagnosis links numerous conditions once regarded as isolated, single-organ diseases that existed outside of any known underlying systemic condition (Table 1). The histopathological findings in IgG4-RD are consistent across the wide range of organ systems that can be involved. IgG4-RD is often confused with a malignancy upon presentation because it has a tendency to form mass lesions. In addition, IgG4-RD can mimic a host of immune-mediated conditions, e.g., primary sclerosing cholangitis, idiopathic interstitial lung disease, Sjogren's syndrome, granulomatosis with polyangiitis, and idiopathic membranous nephropathy." @default.
- W2567103616 created "2017-01-06" @default.
- W2567103616 creator A5042482253 @default.
- W2567103616 date "2016-01-27" @default.
- W2567103616 modified "2023-09-27" @default.
- W2567103616 title "IgG4-Related Disease: Diagnostic Testing by Serology, Flow Cytometry, and Immunohistopathology" @default.
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- W2567103616 doi "https://doi.org/10.1128/9781555818722.ch95" @default.
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