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IgG4-related disease : why high IgG4 and fibrosis? [PDF]
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
Clinical Images: Features of IgG4‐related disease in a patient with granulomatosis with polyangiitis
ACR Open Rheumatology, Volume 8, Issue 8, August 2026.
Florian Kollert +9 more
wiley +1 more source
In IgG4‐related disease, the epithelial‐to‐mesenchymal transition of fibroblasts was predominantly driven by transforming growth factor‐β1 secreted from CD19+ B cells. Reciprocally, fibroblasts facilitated CD19+ B‐cell survival and activation through CXCL14–CXCR4 and CXCL12–CXCR4 signalling axes, thereby promoting B‐cell responses and subsequent ...
In‐Woon Baek +2 more
wiley +1 more source
Additional file 4. Other differences among Clusters. a, Distribution of the grades of complement in clusters. Normal values of C3 and C4 were 0.73-1.46 and 0.1-0.4(g/L), respectively. b, Distribution of the grades of IgG4-RD CS in clusters. (CS1, range-1.
Liang Zhu (172992) +12 more
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AEG‐AESPANC‐OPGE‐SIED‐SPG Ibero‐Latin American Guidelines on Acute Pancreatitis (iLATAM‐AP)
ABSTRACT Introduction Acute pancreatitis (AP) is a major cause of gastrointestinal hospitalizations worldwide. Although typically self‐limiting, up to one‐third of cases develop complications associated with increased morbidity and mortality. Despite recent advances that have improved outcomes, clinical heterogeneity necessitates updated, evidence ...
Karina Cárdenas‐Jaén +44 more
wiley +1 more source
IntroductionWell-differentiated liposarcoma (WDLPS) is a locally aggressive soft tissue sarcoma characterized by the amplification of MDM2 and/or CDK4.
Naoki Oike +10 more
doaj +1 more source
IgG4-related disease (IgG4-RD) is a systemic autoimmune disease with unclear pathogenesis. We performed single-cell RNA-seq and surface proteome analyses on 61,379 PBMCs from 9 treatment-naive IgG4-RD patients and 7 age- and sex-matched healthy controls.
Chenyang Lu +15 more
doaj +1 more source
The spectrum of Castleman diseases has expanded over the past three decades. The phenotype of the diseases varies not only among the three major types but also according to the patient ancestry. Summary Under the Castleman disease (CD) eponym, three distinct diseases sharing common pathological features have been described over time.
Eric Oksenhendler +4 more
wiley +1 more source
Profiles of IgG4-RD patients analyzed by DNA microarrays.
Patients were diagnosed according to the comprehensive diagnostic criteria for IgG4-RD [6] and were subsequently treated with steroids. IgG(mg/dL), IgG4(mg/dL), IgE(IU/mL).
Motohisa Yamamoto (739148) +31 more
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[18F]FAPI PET/CT-based scoring systems for patient assessment in IgG4-related disease
Background 18F-Fibroblast activation protein inhibitor ([18F]FAPI) positron emission tomography (PET)/CT is an emerging tool for detecting IgG4-related disease (IgG4-RD).
Zhenfeng Liu +6 more
doaj +1 more source

