ArticleRheumatology advances in practice2019
Retrospective single-centre analysis of IgG4-related disease patient population and treatment outcomes between 2007 and 2017.
Article in Rheumatology advances in practice, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
6 citing papers in PubMed.
- Article
- IgG4-Related Disease: Emerging Roles of Novel Genetic Variants, Immune Cell Subsets and Therapeutic Targets.Allergy · 2025Review
- An Unusual Presentation of Immunoglobulin G4-Related Disease (IgG4-RD) Causing Subglottic Stenosis.Cureus · 2022Article
- Natural developing process of immunoglobulin G4-related sialadenitis after submandibular gland excision: a retrospective cohort study.Clinical rheumatology · 2021Article
- Two cases of immunoglobulin G4 (IgG4)-related hypophysitis diagnosed without pituitary biopsy.Therapeutic advances in endocrinology and metabolism · 2020Article
- Tumour of the orbit and pterygopalatine fossa: delayed recognition of possible IgG4-related disease.Contemporary oncology (Poznan, Poland) · 2020Article
Corrections and comments
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveThe aim was to gain a better understanding of the prevalence, organ involvement, clinical characteristics and long-term outcomes of medical and surgical treatments of IgG4-related disease (IgG4-RD).
methodsQuery of the Cleveland Clinic pathology database for IgG4 plasma cell staining between 2007 and 2017 yielded 1481 results, of which 57 cases were identified as highly likely (
resultsOf all patients who met the IgG4 staining criteria (
conclusionA histological diagnosis of IgG4-RD could be made in half of the patients who had IgG4
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Registered trials
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