Evidence map›Paper›PMID 34618230›Full record

ArticleVirchows Archiv : an international journal of pathology2022

Mass-forming immunoglobulin G4-related disease shows indolent clinical course after surgical resection, clinicopathological analysis of a series of 15 cases.

Ruoyu Shi, Benjamin Livingston Farah, Chuanhui Xu, Joe Poh Sheng Yeong, Chik Hong Kuick, Jian Yuan Goh, Kenneth Tou En Chang, Angela Takano

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Article in Virchows Archiv : an international journal of pathology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
–field-weighted citation impact, top 81% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 1 country.

Ruoyu ShiDepartment of Anatomical Pathology, Singapore General Hospital, Singapore, 169856, Singapore. shi.ruoyu@singhealth.com.sg.ORCID http://orcid.org/0000-0001-8292-4044
Benjamin Livingston FarahDepartment of Anatomical Pathology, Singapore General Hospital, Singapore, 169856, Singapore.ORCID http://orcid.org/0000-0002-0911-6734
Chuanhui XuDepartment of Rheumatology Allergy and Immunology, Tan Tock Seng Hospital, Singapore, Singapore.ORCID http://orcid.org/0000-0002-3222-7168
Joe Poh Sheng YeongDepartment of Anatomical Pathology, Singapore General Hospital, Singapore, 169856, Singapore.ORCID http://orcid.org/0000-0002-6674-7153
Chik Hong KuickDepartment of Pathology and Laboratory Medicine, KK Women's and Children's Hospital, Singapore, Singapore.
Jian Yuan GohDepartment of Pathology and Laboratory Medicine, KK Women's and Children's Hospital, Singapore, Singapore.ORCID http://orcid.org/0000-0003-4562-7475
Kenneth Tou En ChangDepartment of Pathology and Laboratory Medicine, KK Women's and Children's Hospital, Singapore, Singapore.ORCID http://orcid.org/0000-0001-5244-4285
Angela TakanoDepartment of Anatomical Pathology, Singapore General Hospital, Singapore, 169856, Singapore.ORCID http://orcid.org/0000-0002-7830-8430
KK Women's and Children's Hospital · SGSingapore General Hospital · SGAgency for Science, Technology and Research · SGSingHealth · SGTan Tock Seng Hospital · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of this study is to characterize the clinicopathological features of mass-forming immunoglobulin G4-related disease (IgG4-RD). A retrospective search for cases of mass-forming IgG4-RD diagnosed at Singapore General Hospital between 2008 and 2019 was performed. A total of 15 cases of mass-forming IgG4-RD were identified. The male-to-female ratio was 2.5:1, and the median age was 61 years old. The majority of cases showed a solitary lesion (12/15) with a mean size of 35 mm. IgG4-RD was considered as a clinical differential diagnosis only in one case (1/15) prior to the surgical resection. Diagnostic histopathological features, such as dense lymphoplasmacytic infiltrate positive for IgG4 plasma cells (15/15), storiform fibrosis (15/15), and obliterative phlebitis (9/15), were observed in most cases. These findings were distributed heterogeneously within the lesions. Cases with single organ involvement showed a low relapse rate (2/10) and normal serum IgG4 level after surgical resection. Mass-forming IgG4-RD has a male predilection and involves various organ systems. It may be initially misdiagnosed as malignancy and undergo surgical resection. The diagnostic histological features of IgG4-RD are readily identified in different organs. However, they may be distributed heterogeneously within a single lesion. Cases of single organ involvement show an indolent clinical course and normal serum IgG4 level after surgical resection.

Indexed as

Immunoglobulin G4-Related DiseaseFemaleFibrosisHumansImmunoglobulin GMaleMiddle AgedPlasma CellsRetrospective StudiesImmunoglobulin GIgG4-related diseaseMass formingPlasma cellsSerum IgG4 levelSingle organ

Identifiers

PMID34618230
OpenAlexW3202373880

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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.