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Abstract and Introduction Abstract Objectives: In IgG4-related disease, the relationship between pathological findings and relapse has not been well established. This study aimed to identify the clinical and pathological predictors of disease relapse in IgG4-RD. Methods: Patients with newly diagnosed IgG4-RD (n = 71) were enrolled between January 2011 and April 2020; all cases were pathologically confirmed.
Introduction Immunoglobulin G (IgG) 4 related disease (IgG4-RD) is a systemic and inflammatory autoimmune disease.1 It is a new type of disease that was named 10 years ago. With advancements in understanding of the disease, the rate of IgG4-RD diagnosis has been steadily increasing. The disease commonly manifests with multiple organ involvement, accompanied by organ fibrosis and even dysfunction.
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