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Clinical Journal of the American Society of Nephrology, 2023
The term “IgG4-related disease” was recently coined to identify a rare systemic disorder hallmarked by fibro-inflammatory, tumor-like masses possibly affecting almost any organ. Pathologic tissues are characterized by dense, polyclonal, lymphoplasmacytic infiltrates, rich in IgG4-positive plasma cells on a background of fibrosis, which often has a ...
Francesco Peyronel, Augusto Vaglio
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The term “IgG4-related disease” was recently coined to identify a rare systemic disorder hallmarked by fibro-inflammatory, tumor-like masses possibly affecting almost any organ. Pathologic tissues are characterized by dense, polyclonal, lymphoplasmacytic infiltrates, rich in IgG4-positive plasma cells on a background of fibrosis, which often has a ...
Francesco Peyronel, Augusto Vaglio
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IgG4-related Disease and the Liver
Gastroenterology Clinics of North America, 2017Pathologists are likely to encounter IgG4-related disease in several organ systems. This article focuses on helping pathologists diagnose IgG4-related disease in the hepatobiliary system. Missing the diagnosis can result in unnecessary organ damage and/or unnecessary surgical and cancer therapy.
Jonathan H, Chen, Vikram, Deshpande
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2016
IgG4-related disease (IgG4-RD) is a fibro-inflammatory condition characterized by fibrous swelling of affected organs, elevated serum IgG4 concentration in the majority of patients, and a prompt response to corticosteroid therapy. The concept of IgG4-RD as a novel clinical entity emerged at the beginning of the twenty-first century, when Hamano and ...
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IgG4-related disease (IgG4-RD) is a fibro-inflammatory condition characterized by fibrous swelling of affected organs, elevated serum IgG4 concentration in the majority of patients, and a prompt response to corticosteroid therapy. The concept of IgG4-RD as a novel clinical entity emerged at the beginning of the twenty-first century, when Hamano and ...
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Management of IgG4-related disease
The Lancet Rheumatology, 2019IgG4-related disease was unrecognised as a unified disease entity until this century, yet in a short period of time the disease has been appreciated to have a worldwide distribution, and its clinical, pathological, and radiological features have been described in considerable detail.
Wen, Zhang, John H, Stone
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The Histopathology of IgG4-Related Disease
2016IgG4-related disease is a multi-organ immune-mediated chronic fibroinflammatory condition characterized by elevated serum IgG4 concentrations, tumefaction, and tissue infiltration by IgG4-positive plasma cells. The exact etiology of IgG4-related disease remains unclear with no known role of the IgG4 molecule itself being identified.
Mehmet Ozgur, Avincsal, Yoh, Zen
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An update on IgG4-related disease
Current Opinion in Rheumatology, 2015IgG4-related disease (IgG4-RD) is a recently described fibroinflammatory condition that can affect nearly any organ. Our knowledge of this condition--its manifestations, diagnosis, pathogenesis and treatment--is expanding rapidly.This review highlights the most recent developments in the field.
Zachary S, Wallace, John H, Stone
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Diagnostic Histopathology, 2012
IgG4-related disease (IgG4-RD) is a recently recognized systemic autoimmune disease that has received increased attention in the literature in the past several years. Renal involvement can take several forms, which are described in this review.IgG4-RD may affect the kidney in various patterns. IgG4-related tubulointerstitial nephritis (TIN), presenting
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IgG4-related disease (IgG4-RD) is a recently recognized systemic autoimmune disease that has received increased attention in the literature in the past several years. Renal involvement can take several forms, which are described in this review.IgG4-RD may affect the kidney in various patterns. IgG4-related tubulointerstitial nephritis (TIN), presenting
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IgG4-Related Ophthalmic Disease
New England Journal of Medicine, 2022Yi-Min Huang, Pei-Hsuan Lin
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Comprehensive diagnostic criteria for IgG4-related disease (IgG4-RD), 2011
Modern Rheumatology, 2012Hisanori Umehara +2 more
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