Case report illustrates IgG4-RD affecting the uterus and lymph nodes, indicating the need for heightened awareness.
Immunoglobulin G4-related disease (IgG4-RD) is a systemic fibroinflammatory disorder that commonly affects multiple organs and may be misdiagnosed when presenting at atypical sites. We report an example of IgG4-RD involving the uterus and abdominopelvic lymph nodes and review the literature to clarify clinical, pathological and laboratory features. A 51-year-old female patient presented with prolonged menstruation and underwent PET/CT that revealed hypermetabolic masses in the uterus and multiple abdominopelvic lymph nodes, initially suggesting malignancy. She underwent a total hysterectomy and lymph node biopsy. Histopathology showed storiform fibrosis, obliterative phlebitis and dense lymphoplasmacytic infiltrates with abundant IgG4-positive plasma cells. Serum IgG4 and IgG levels were markedly elevated, supporting the diagnosis of IgG4-RD. Postoperative therapy with a regimen comprising dexamethasone, cyclophosphamide and bortezomib resulted in a substantial reduction in serum IgG4 levels, indicating effective disease management. This case report emphasizes the need to consider IgG4-RD in unusual anatomical locations, to enhance clinical awareness, and to apply comprehensive diagnostic criteria to improve patient outcomes.
No takes yet. Share an insight, caveat, or question.
Qingyun et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: