Autoimmune pancreatitis and IgG4-related systemic diseases.
Abstract
Autoimmune pancreatitis (AIP) is a rare form of chronic pancreatitis that is characterized by lymphoplasmacytic infiltrate, storiform fibrosis, obliterative phlebitis, and increased IgG4(+) plasma cells. Serum IgG4 levels usually are elevated. Patients with AIP frequently have disease affecting other organs or sites; these tissues show similar histologic changes, including increased IgG4(+) plasma cell infiltrate and response to corticosteroid...
Paper Details
Title
Autoimmune pancreatitis and IgG4-related systemic diseases.
Published Date
May 25, 2010
Journal
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Notes
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