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10.4103/tjo.tjo_12_17 http://scihub22266oqcxt.onion/10.4103/tjo.tjo_12_17 C5890589!5890589!29675343     free     free     free Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\29675343.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Taiwan+J+Ophthalmol 2018 ; 8 (1): 9-14 Nephropedia Template TP {{tp|p=29675343|t=2018. Immunoglobulin G4-related ophthalmic disease |pdf=|usr=}}{{29675343}} gab.com Text Immunoglobulin G4-related ophthalmic disease JO: Taiwan J Ophthalmol http://www.kidney.de/pget.php?&tw=1&pmid=29675343 #FOAvip 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 IgG4-related ophthalmic disease (IgG4-ROD) is generally recognized as the disease name. A significant proportion of previous labeled idiopathic orbital inflammations and Mikulicz's disease are now consistent with a diagnosis of IgG4-ROD. Increasing studies have accumulated regarding its epidemiology, diagnosis, clinical features, treatment, and the association between lymphoma. In this review, we summarize our present understanding of IgG4-ROD. Twit Text FOAVip Immunoglobulin G4-related ophthalmic disease ????Taiwan J Ophthalmol http://www.kidney.de/pget.php?&tw=1&pmid=29675343 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29675343 #FOAvip English Wikipedia <ref>{{Cite pmid|29675343}}</ref> Immunoglobulin G4-related ophthalmic disease #MMPMID29675343 Yu WK; Tsai CC; Kao SC; Liu CJL Taiwan J Ophthalmol 2018[Jan]; 8 (1): 9-14 PMID29675343show ga 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 IgG4-related ophthalmic disease (IgG4-ROD) is generally recognized as the disease name. A significant proportion of previous labeled idiopathic orbital inflammations and Mikulicz's disease are now consistent with a diagnosis of IgG4-ROD. Increasing studies have accumulated regarding its epidemiology, diagnosis, clinical features, treatment, and the association between lymphoma. In this review, we summarize our present understanding of IgG4-ROD. äImmunoglobulin G4-related ophthalmic disease (epmc).pdf DeepDyve Pubget Overpricing