Evidence map›Paper›PMID 39085476›Full record

ArticleSkeletal radiology2025

IgG4-related disease with subcutaneous involvement and the associated diagnostic challenges with MRI.

Tomonori Kawasaki, Jiro Ichikawa, Kojiro Onohara, Satoshi Kanno, Masanori Wako, Naofumi Taniguchi, Satoshi Ochiai, Tomoaki Torigoe, Yasuo Yazawa

Abstract readCase Reports
In one paragraph

Article in Skeletal radiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. [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 · 2025
    Article
  2. Article
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

9 authors.

Tomonori KawasakiDepartment of Pathology, Saitama Medical University International Medical Centre, Saitama, Japan.
Jiro IchikawaDepartment of Orthopaedic Surgery, Interdisciplinary Graduate School of Medicine, University of Yamanashi, Yamanashi, Japan. jichi@sb4.so-net.ne.jp.ORCID http://orcid.org/0000-0002-9850-6047
Kojiro OnoharaInterdisciplinary Graduate School of Medicine, University of Yamanashi, Yamanashi, Japan.
Satoshi KannoDepartment of Pathology, Saitama Medical University International Medical Centre, Saitama, Japan.
Masanori WakoDepartment of Orthopaedic Surgery, Interdisciplinary Graduate School of Medicine, University of Yamanashi, Yamanashi, Japan.
Naofumi TaniguchiDepartment of Orthopaedic Surgery, Interdisciplinary Graduate School of Medicine, University of Yamanashi, Yamanashi, Japan.
Satoshi OchiaiDepartment of Orthopaedic Surgery, National Hospital Organization (NHO) Kofu National Hospital, Kofu, Yamanashi, Japan.
Tomoaki TorigoeOrthopaedic Oncology & Surgery, Saitama Medical University International Medical Centre, Saitama, Japan.
Yasuo YazawaOrthopaedic Oncology & Surgery, Saitama Medical University International Medical Centre, Saitama, Japan.

Funding

joint research grants from the Comprehensive Agreement between Saitama University and Saitama Medical University 21-J-14joint research grants from the Comprehensive Agreement between Saitama University and Saitama Medical University 22-J-01joint research grants from the Comprehensive Agreement between Saitama University and Saitama Medical University 23-J-08
6 · The paper itself

Abstract

IgG4-related disease is a rare fibroinflammatory disorder characterized by the infiltration of IgG4-rich plasma cells. Herein, we report a case of IgG4-related disease of the subcutaneous tissue with atypical MRI findings and difficulties in the histopathological examination using needle biopsy. Based on the clinical presentation and MRI findings, the patient was diagnosed with a benign myxoid or cystic tumor. Additionally, histopathological findings from a needle biopsy suggested a myxoma. Therefore, the correct diagnosis of IgG4-related disease was not made preoperatively. The resected specimens confirmed IgG4-related disease with an IgG4/IgG ratio > 80%. Previous reports have shown that the MRI findings of IgG4-related disease mimic both malignancy and inflammation; surprisingly, the features of subcutaneous IgG-related disease, including tail sign, unclear border, and heterogeneous enhancement, were similar to those found in sarcoma. Therefore, histopathological findings are needed for a correct diagnosis. Furthermore, careful examination is essential because the neoplasm and inflammation may overlap with IgG4-related disease, and needle biopsy is not fully reflective of the tumor. As is highlighted in the present case, IgG4-related disease is often misdiagnosed; therefore, clinicians should adequately recognize that even if the histopathological findings in biopsy were consistent with those observed in the MRI, misdiagnosis may occur.

Indexed as

Immunoglobulin G4-Related DiseaseMagnetic Resonance ImagingSubcutaneous TissueBiopsy, NeedleDiagnosis, DifferentialHumansImmunoglobulin GImmunoglobulin GBiopsyDifferential diagnosisHistopathologyIgG4-related diseaseMRISubcutaneous

Identifiers

PMID39085476
PMCPMC11953168

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Registered trials

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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.