Evidence map›Paper›PMID 39889160›Full record

ArticleMedicine2025

Concurrent ANCA-associated vasculitis and IgG4-related disease in a patient with fever of unknown origin and acute kidney injury: A case report.

Soo Jin Lee, Yujin Shin, Seung Ah Cha, Kyoung Min Kim, Kyung Pyo Kang

Abstract readCase Reports
In one paragraph

Article in Medicine, 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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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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

5 authors.

Soo Jin LeeDepartment of Internal Medicine, Jeonbuk National University Hospital, Jeonju, Korea.
Yujin ShinDepartment of Internal Medicine, Jeonbuk National University Hospital, Jeonju, Korea.
Seung Ah ChaDepartment of Internal Medicine, Jeonbuk National University Hospital, Jeonju, Korea.
Kyoung Min KimDepartment of Pathology, Jeonbuk National University Medical School, Jeonju, Korea.
Kyung Pyo KangDepartment of Internal Medicine, Jeonbuk National University Hospital, Jeonju, Korea.ORCID 0000-0001-8720-9701

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleIt is often challenging to differentiate between IgG4-related disease (IgG4-RD) and antineutrophil cytoplasmic antibody-associated vasculitis (AAV) due to their similar clinical presentations. Recently, growing evidence has suggested a strong connection between AAV and IgG4-RD. PATIENT CONCERNS: A 60-year-old woman was transferred to our hospital with fever and kidney dysfunction. Abdominal computed tomography revealed widespread infiltrative lesions in both kidneys. DIAGNOSES: Laboratory tests and subsequent renal biopsy confirmed both antineutrophil cytoplasmic antibody-associated vasculitis and IgG4-related disease.

interventionsWe initiated plasmapheresis, oral cyclophosphamide, and high-dose glucocorticoids for treatment. Despite this, the patient's condition worsened, requiring emergency hemodialysis. OUTCOMES: After 3 months of continued immunosuppressive treatment, renal function improved and hemodialysis was discontinued. LESSONS: Our case showed an overlap of AAV and IgG4-RD, which might support the hypothesis of an overlap syndrome of AAV and IgG4-RD. Clinicians should have a high index of suspicion when diagnosing fever of unknown origin, with the possibility of overlapping AAV and IgG4-RD.

Indexed as

Acute Kidney InjuryAnti-Neutrophil Cytoplasmic Antibody-Associated VasculitisFever of Unknown OriginImmunoglobulin G4-Related DiseaseCyclophosphamideDiagnosis, DifferentialFemaleGlucocorticoidsHumansImmunoglobulin GImmunosuppressive AgentsMiddle AgedPlasmapheresisCyclophosphamideGlucocorticoidsImmunoglobulin GImmunosuppressive Agents

Identifiers

PMID39889160
PMCPMC11789897

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