Evidence map›Paper›PMID 40751168›Full record

ArticleBMC rheumatology2025

IgG4-related disease with interstitial nephritis in a patient with metastatic melanoma following immune checkpoint inhibitor treatment: a case report.

Thabuna Sivaprakasam, Prachaya Nitchaikulvatana, Jodi Gedallovich, Jagruti Shah, Matthew Charles Baker

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Article in BMC rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Thabuna SivaprakasamDepartment of Internal Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, SD, USA. thabuna.siva@gmail.com.
Prachaya NitchaikulvatanaDepartment of Medicine, Division of Immunology and Rheumatology, Stanford University, Palo Alto, CA, USA.
Jodi GedallovichDepartment of Pathology, Stanford University, Palo Alto, CA, USA.
Jagruti ShahDivision of Nuclear Medicine and Molecular Imaging, Department of Radiology, Stanford University, Stanford, CA, USA.
Matthew Charles BakerDepartment of Medicine, Division of Immunology and Rheumatology, Stanford University, Palo Alto, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs) have become a cornerstone in the treatment of metastatic melanoma. Several case reports have documented IgG4-related disease (IgG4-RD) as an adverse event following ICI therapy. Here we report the first instance of interstitial nephritis associated with IgG4-RD as an immune-related adverse event (irAE) following ICI treatment. CASE PRESENTATION: A 71-year-old male with malignant melanoma (BRAF wild-type) initially received one cycle of adjuvant pembrolizumab, followed by four cycles of ipilimumab/nivolumab after the occurrence of lung metastases. Four months later, a follow-up computed tomography (CT) revealed infiltrative masses in the kidneys, along with abnormal mediastinal and hilar lymphadenopathy but his baseline serum creatinine remained stable. A subsequent kidney biopsy showed renal parenchyma with significant interstitial nephritis and an increase in IgG4-positive plasma cells, with no evidence of malignancy. Plasma IgG4 levels were elevated at 294 mg/dL (normal 11-157 mg/dL), and complement C4 level was low at < 8 mg/dL. In addition, the patient had an asymptomatic rise in lipase (105 U/L, normal 7-60 U/L), but had no other findings to suggest pancreatitis. The patient was started on prednisone 40 mg daily with a plan to taper. A follow-up CT scan performed four weeks later showed near-complete resolution of the previously observed mediastinal lymphadenopathy and bilateral infiltrative renal masses.

conclusionThis represents the first reported case of interstitial nephritis resulting from IgG4-related disease following ICI treatment. Clinicians should consider the potential for IgG4-RD, particularly with associated renal manifestations, in patients undergoing ICI therapy. Early recognition and treatment of this rare side effect can significantly impact the clinical outcome. This case highlights the importance of being vigilant for uncommon and new adverse effects following ICI treatment, especially as the field continues to evolve and new immunotherapies are developed. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Case reportIgG4-related diseaseImmune checkpoint inhibitorsImmune-related adverse eventsInterstitial nephritisIplimumabNivolumabPembrolizumab

Identifiers

PMID40751168
PMCPMC12315461

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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.