Immunoglobulin G4-related ophthalmic disease
Abstract
Immunoglobulin G4-related disease (IgG4-RD) is a recently recognized inflammatory disease of unknown etiology. It characterized by distinctive histopathological appearance of dense IgG4-positive lymphoplasmacytic infiltrates, storiform fibrosis, and obliterative phlebitis in one or more organs, simultaneously or subsequently. In cases of ocular adnexal involvement, unique clinicohistopathological features were delineated by recent studies, and...
Paper Details
Title
Immunoglobulin G4-related ophthalmic disease
Published Date
Jan 1, 2018
Volume
8
Issue
1
Pages
9 - 9
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