Results 61 to 70 of about 609,847 (198)
IgG4-related sclerosing disease
World Journal of Gastroenterology, 2008 Based on histological and immunohistochemical examination of various organs of patients with autoimmune pancreatitis (AIP), a novel clinicopathological entity of IgG4-related sclerosing disease has been proposed. This is a systemic disease that is characterized by extensive IgG4-positive plasma cells and T-lymphocyte infiltration of various organs ...
Terumi, Kamisawa, Atsutake, Okamoto
openaire +2 more sources
IgG4-Related Disease and Malignancy
Internal Medicine, 2012 Mikulicz’s disease (MD) has been included within the diagnosis of primary Sjogren’s syndrome (SS), but it represents a unique condition involving the enlargement of the lacrimal and salivary glands and characterized by few autoimmune reaction (1). Glucocorticoid treatment is effective for the clinical improvement of this disease (2).
Yamamoto, Motohisa +2 more
openaire +3 more sources
Topiramate-induced maculopathy in IgG4-related disease
, 2016 Joanna DaCosta,1,2 Saad Younis1 1Ophthalmology Department, Imperial College Healthcare NHS Trust, Western Eye Hospital, 2Barts Health NHS Trust, Whipps Cross University Hospital, London, UK Abstract: This report describes a case of reversible topiramate-
DaCosta J, Younis S
core
IgG4-related disease: current challenges and future prospects
, 2016 David Lang,1 Jochen Zwerina,2 Herwig Pieringer1,3 1Second Department of Internal Medicine, Kepler University Clinic, Linz, 2First Department of Internal Medicine, Ludwig Boltzmann-Institute of Osteology, Hanusch Hospital, Vienna, 3Paracelsus ...
Lang D, Pieringer H, Zwerina J
core
Frontiers in ImmunologyBackgroundImmunoglobulin G4-related disease (IgG4-RD) is an immune-mediated chronic fibroinflammatory condition that can affect multiple organ systems. IgG4-related sclerosing cholangitis (IgG4-SC) is its manifestation involving the biliary tract. Due to
Ying-Ao Liu +6 more
doaj +1 more source
Rosai-Dorfman disease (RDD), or sinus histiocytosis with massive lymphadenopathy, is a rare histiocytic disorder that often mimics malignancies and immune-mediated conditions such as IgG4-related disease (IgG4-RD).
Julia Maria Sołek +6 more
core +1 more source
An update on IgG4-related lung disease
, 2019 IgG4-related disease (IgG4-RD) is an autoimmune disorder characterized by substantial infiltration of plasma cells with IgG4 in target organs. Lung manifestations predominantly present as inflammatory pseudotumor, interstitial pneumonitis, organizing ...
Mirsaeidi, Mehdi +4 more
core +1 more source
Acta Dermato-Venereologica, 2018 Systemic plasmacytosis is a rare skin disorder characterized by marked infiltration of plasma cells in the dermis. IgG4-related disease is pathologically characterized by lymphoplasmacytic infiltration rich in IgG4+ plasma cells, storiform fibrosis, and ...
Shintaro Takeoka +12 more
doaj +1 more source
Renal Manifestations of IgG4-Related Disease: A Concise Review
International Journal of NephrologyIgG4-related disease (IgG4-RD) is an immune-mediated disorder marked by fibro-inflammatory masses that can infiltrate multiple organ systems. Due to its relatively recent discovery and limited understanding of its pathophysiology, IgG4-related disease ...
Shahrukh T. Towheed +4 more
doaj +1 more source
IgG4-related disease : why high IgG4 and fibrosis? [PDF]
, 2013 The hallmarks of IgG4-related disease (IgG4-RD) are lymphoplasmacytic tissue infiltration with a predominance of IgG4-positive plasma cells, accompanied by fibrosis, obliterative phlebitis, dacryoadenitis, and elevated levels of IgG4.
Koike, Takao
core +1 more source