ReviewProceedings of the Japan Academy. Series B, Physical and biological sciences2018
Current perspectives on autoimmune pancreatitis and IgG4-related disease.
Review in Proceedings of the Japan Academy. Series B, Physical and biological sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
21 citing papers in PubMed, 56 citations in OpenAlex.
- Necrotizing pancreatitis with multifocal hepatic artery pseudoaneurysms: Diagnostic limitations and rare appearance of suspected IgG-4 related disease.Radiology case reports · 2026Article
- Correlations between IgG4-related disease, autoimmune pancreatitis, and allergic diseases.Frontiers in immunology · 2026Review
- [Analysis of clinical characteristics and current diagnosis and treatment status of IgG4-related diseases in the real world].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2025Article
- Differentiating pancreatic ductal adenocarcinoma and autoimmune pancreatitis using a machine learning model based on ultrasound clinical features.Frontiers in oncology · 2025Article
- A Case Report of a Challenging Disease: Immunoglobulin G4-Related Disease With Acute Kideny Injury.Journal of medical cases · 2023Article
- Main Diagnostic Criteria Usually Does Not Work for Autoimmune Pancreatitis Wrongly Presuming Malignancy.Gastroenterology research and practice · 2023Article
- Immunoglobulin G4-related disease involving multiple systems: A case report.World journal of clinical cases · 2022Article
- Review
- Retrospective Analysis of the Value of Enhanced CT Radiomics Analysis in the Differential Diagnosis Between Pancreatic Cancer and Chronic Pancreatitis.International journal of general medicine · 2022Article
- Multimodel magnetic resonance imaging of mass-forming autoimmune pancreatitis: differential diagnosis with pancreatic ductal adenocarcinoma.BMC medical imaging · 2021Article
- Immunoglobulin G4-related disease: case report and literature review.Immunologic research · 2021Review
- Multidisciplinary treatment of chronic active Epstein-Barr virus infection with multiple complications: a case report.Translational pediatrics · 2021Article
- Multisystem IgG4-related disease involving the abdomen and coronary arteries and causing chronic abdominal pain.Acta radiologica open · 2021Article
- Article
- Clinical characteristics and long-term prognosis of autoimmune pancreatitis with renal lesions.Scientific reports · 2021Article
- Fevers, Sweats, Weight Loss, Oh My! When IgG4 Related Disease Comes Knocking. . .Clinical medicine insights. Case reports · 2021Article
- Autoimmune Hepatitis with Elevated Serum IgG4 Levels Have a High Prevalence of Cirrhosis at Diagnosis.Canadian journal of gastroenterology & hepatology · 2021Article
- Feline comorbidities: What do we really know about feline triaditis?Journal of feline medicine and surgery · 2020Review
- Steroid-responsive pancreatitides.World journal of clinical cases · 2020Review
- The Cellular and Molecular Bases of Allergy, Inflammation and Tissue Fibrosis in Patients with IgG4-related Disease.International journal of molecular sciences · 2020Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
IgG4-related disease (IgG4-RD) is a fibroinflammatory disorder recognized as a novel clinical entity with either synchronous or metachronous multi-organ involvement. Patients with IgG4-RD show diffuse or focal organ enlargement and mass-forming or nodular/thickened lesions with abundant infiltration of IgG4-positive plasmacytes and fibrosis, and such patients respond well to steroid treatment. It should be differentiated from mimics by a combination of serum IgG4 level, imaging features, and histopathological findings. The current first-line drug is corticosteroids, or rituximab in high-risk patients for steroid intolerance. Although relapse rates are high, standardized protocols for relapsed cases have not been approved yet. Based on genetic factors, disease-specific or -related antigens, abnormal innate and adaptive immunity may be involved, although the precise pathogenic mechanism and long-term outcome still remain unclear.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.