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Immunoglobulin G4-related disease (IgG4-RD) is a systemic immune-mediated condition that can affect multiple organs. Prostatic involvement, although uncommon, may closely mimic prostate cancer due to the presence of a prostatic mass and elevated prostate-specific antigen (PSA) levels. In rare cases, IgG4-related prostatitis occurs in isolation, without evidence of other organ involvement. We present the case of a 78-year-old man initially suspected of having prostate cancer based on a markedly elevated PSA level and prostate magnetic resonance imaging findings. However, prostate biopsy revealed no malignancy, instead showing dense infiltration of IgG4-positive plasma cells. Along with elevated serum IgG4 levels, these findings led to a diagnosis of isolated IgG4-related prostatitis. The patient initially declined treatment, but over the following two years, his prostate volume increased, and his dysuria, characterized by urinary frequency, difficulty urinating, and a sensation of post-void residual urine, worsened. Initiation of prednisolone therapy resulted in normalization of serum IgG4 levels and marked improvement in both prostate swelling and urinary function. A literature review identified only three additional reported cases of isolated IgG4-related prostatitis. This case highlights the potential for prostate-limited IgG4-RD and underscores the importance of including IgG4-related prostatitis in the differential diagnosis of suspected prostate cancer, particularly when biopsy findings are atypical.
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http://dx.doi.org/10.1007/s00296-025-05960-x | DOI Listing |
Rheumatol Int
August 2025
Kaneko Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, 160-8582, Tokyo, Japan.
Immunoglobulin G4-related disease (IgG4-RD) is a systemic immune-mediated condition that can affect multiple organs. Prostatic involvement, although uncommon, may closely mimic prostate cancer due to the presence of a prostatic mass and elevated prostate-specific antigen (PSA) levels. In rare cases, IgG4-related prostatitis occurs in isolation, without evidence of other organ involvement.
View Article and Find Full Text PDFMod Rheumatol Case Rep
July 2025
Department of Clinical Immunology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
We report a case of a 64-year-old Japanese man who developed IgG4-related pericoronary arteritis following mRNA-based COVID-19 vaccination. The patient presented with anterior chest pain and imaging revealed perivascular soft tissue thickening around the coronary arteries, along with pancreatic enlargement, enlarged prostate, and periaortitis. Laboratory tests showed markedly elevated serum IgG4 levels (1740 mg/dl).
View Article and Find Full Text PDFNephrology (Carlton)
January 2025
Division of Nephrology, Department of Internal Medicine, Faculty of Medicine, Thammasat University, Pathumthani, Thailand.
The case report presents a male patient in his mid-60s with a history of hypertension, benign prostatic hyperplasia and chronic kidney disease (CKD). He presented with gradually increasing serum creatinine levels and hyperglobulinemia, leading to suspicion of multiple myeloma. However, subsequent testing revealed features consistent with systemic lupus erythematosus (SLE) and IgG4-related kidney disease (IgG4-RKD).
View Article and Find Full Text PDFBackground: Autoimmune pancreatitis (AIP) is a form of chronic pancreatitis that presents clinically with obstructive icterus, histologically with infiltration of pancreatic parenchyma by inflammatory cells leading to chronic inflammation with fibrosis, and therapeutically with good response to corticosteroid therapy. Clinically, it may resemble malignant disease, making diagnosis difficult and requiring a multidisciplinary team (gastroenterologist, endoscopist, radiologist, surgeon, pathologist). Two types of AIP are distinguished.
View Article and Find Full Text PDFJ Hematop
December 2024
University of Vermont Medical Center, Burlington, USA.
A 69-year-old with well-controlled HIV was evaluated for persistent cough, in the context of years of fatigue and influenza A infection 6 months prior. Chest CT and PET scans were notable for adenopathy concerning for a lymphoproliferative disorder. Radiologic studies also showed diffuse FDG uptake in the prostate, consistent with prostatitis.
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