دورية أكاديمية

An Overview of Immunoglobulin G4-related Ophthalmic Diseases Accompanied by a Case Report.

التفاصيل البيبلوغرافية
العنوان: An Overview of Immunoglobulin G4-related Ophthalmic Diseases Accompanied by a Case Report.
المؤلفون: ŞİMŞEK, Bengü ÇOBANOĞLU, CECİKOĞLU, Gözde Ecem, DURMUŞ, Ebubekir, ORHAN SÖYLEMEZ, Umut Perçem
المصدر: Türkiye Klinikleri Journal of Case Reports; 2021, Vol. 29 Issue 1, p33-37, 5p
مصطلحات موضوعية: IMMUNOGLOBULIN G, PLASMA cell diseases, EYE diseases, HISTOPATHOLOGY, EOSINOPHIL disorders
مستخلص: Immunoglobulin G4-related diseases (IgG4-RDs) are immune-mediated, fibroinflammatory conditions that are characterised by affected organ enlargement, lymphocyte, plasma cell infiltration (determined with IgG4-positive plasma cells) and serum IgG4 level elevation. When the disease affects ocular adnexal tissues (such as the lacrimal gland, extraocular muscles, trigeminal nerve branches and orbital fat), it is called IgG4-related ophthalmic disease (IgG4-ROD). The diagnosis of IgG4-ROD is made by physical examination, biochemical findings and histopathological evaluation. It is characterized by elevated serum IgG4 levels and distinctive histopathological features, including IgG4+ plasma cell infiltration, the presence of fibrosis in the storiform pattern and the presence of a dense lymphoplasmacytic inflammatory infiltrate, including eosinophils. It is rare in the ocular region and cause diagnostic confusion. There is a high probability of misdiagnosis when the disease is not recognized. Here, a rare case of eye involvement is presented and IgG4-RDs are discussed with the literature. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index