# Primary bladder diffuse large B-cell lymphoma: a rare case report and literature review

**Authors:** Ya Li, Xianwen Hu, Jiong Cai

PMC · DOI: 10.3389/fmed.2025.1613673 · Frontiers in Medicine · 2025-07-21

## TL;DR

A rare case of bladder lymphoma is reported, highlighting how a diuretic-enhanced PET/CT scan improved diagnosis and treatment monitoring.

## Contribution

Demonstrates the clinical utility of dual-phase 18F-FDG PET/CT with diuretics in diagnosing and staging bladder lymphoma.

## Key findings

- Diuretic-enhanced delayed PET/CT imaging revealed a focal bladder lesion obscured in initial scans.
- The approach enabled accurate staging and confirmed complete remission after chemotherapy.
- This method improves lesion visualization and has significant clinical value for PB-DLBCL.

## Abstract

Primary bladder diffuse large B-cell lymphoma (PB-DLBCL) is an exceedingly rare form of non-Hodgkin lymphoma, accounting for only 0.2% of all extranodal lymphomas. Here we report a case of PB-DLBCL in a woman presenting with hematuria. To determine the disease stage, an 18F-FDG PET/CT scan was performed after surgery. However, intense physiological 18F-FDG activity within the bladder lumen obscured potential lesions and concurrent CT imaging revealed suboptimal bladder distension limiting anatomical delineation. To address these limitations, 20 mg of intravenous furosemide was administered. Delayed imaging was performed 2 h after 18F-FDG injection (1 h after diuretic administration), revealing a focal hypermetabolic lesion in the left bladder wall. This metabolic pattern confirmed the diagnosis of PB-DLBCL, staged as IE according to the Ann Arbor classification. Following 4 cycles of R-CHOP chemotherapy, an 18F-FDG PET/CT scan was performed for treatment response assessment, confirming complete metabolic remission of the PB-DLBCL. This case highlights that dual-phase 18F-FDG PET/CT with intravenous diuretics can reduce bladder background activity and improve lesion visualization. Moreover, this approach holds significant clinical value in assisting with disease staging and evaluating treatment response.

## Linked entities

- **Chemicals:** 18F-FDG (PubChem CID 68614), furosemide (PubChem CID 3440)
- **Diseases:** diffuse large B-cell lymphoma (MONDO:0018905), non-Hodgkin lymphoma (MONDO:0018908)

## Full-text entities

- **Genes:** CCND1 (cyclin D1) [NCBI Gene 595] {aka BCL1, D11S287E, PRAD1, U21B31}, MS4A1 (membrane spanning 4-domains A1) [NCBI Gene 931] {aka B1, Bp35, CD20, CVID5, FMC7, LEU-16}, CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}, CD22 (CD22 molecule) [NCBI Gene 933] {aka SIGLEC-2, SIGLEC2}, CD5 (CD5 molecule) [NCBI Gene 921] {aka LEU1, T1}, PTPRC (protein tyrosine phosphatase receptor type C) [NCBI Gene 5788] {aka B220, CD45, CD45R, GP180, IMD105, L-CA}, MME (membrane metalloendopeptidase) [NCBI Gene 4311] {aka CALLA, CD10, CMT2T, NEP, SCA43, SFE}, PAX5 (paired box 5) [NCBI Gene 5079] {aka ALL3, BSAP, PAX-5}, MYC (MYC proto-oncogene, bHLH transcription factor) [NCBI Gene 4609] {aka MRTL, MYCC, bHLHe39, c-Myc}, PWWP3A (PWWP domain containing 3A, DNA repair factor) [NCBI Gene 84939] {aka EXPAND1, HSPC211, MUM-1, MUM1}, CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, BTK (Bruton tyrosine kinase) [NCBI Gene 695] {aka AGMX1, AT, ATK, BPK, IGHD3, IMD1}, GATA3 (GATA binding protein 3) [NCBI Gene 2625] {aka HDR, HDRS}, CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}, CR2 (complement C3d receptor 2) [NCBI Gene 1380] {aka C3DR, CD21, CR, CVID7, SLEB9}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, BCL6 (BCL6 transcription repressor) [NCBI Gene 604] {aka BCL5, BCL6A, LAZ3, ZBTB27, ZNF51}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}
- **Diseases:** fever (MESH:D005334), Extranodal lymphoma (MESH:D008223), bladder cancer (MESH:D001749), Tumors (MESH:D009369), chronic hepatitis B (MESH:D019694), immune dysregulation (OMIM:614878), NOS (MESH:C536665), fibrosis (MESH:D005355), DLBCL (MESH:D016403), voiding difficulty (MESH:C537271), nocturia (MESH:D053158), MALT lymphoma (MESH:D018442), bone metastases (MESH:D009362), bone marrow hyperplasia (MESH:D001855), non-Hodgkin lymphoma (MESH:D008228), hematologic malignancies (MESH:D019337), chronic (MESH:D002908), mechanical (MESH:D041781), bladder (MESH:D001745), hepatitis B (MESH:D006509), urothelial carcinoma (MESH:D014523), IE (MESH:C566577), dysuria (MESH:D053159), UTIs (MESH:D014552), abdominal/back pain (MESH:D015746), primary (MESH:D010538), Hematuria (MESH:D006417), flank pain (MESH:D021501)
- **Chemicals:** nitrite (MESH:D009573), oncovin (MESH:D014750), rituximab (MESH:D000069283), H&amp;E (MESH:D006371), furosemide (MESH:D005665), 18F-FDG (MESH:D019788), R-CHOP (-), cyclophosphamide (MESH:D003520), hydroxydaunorubicin (MESH:D004317), prednisone (MESH:D011241)
- **Species:** Homo sapiens (human, species) [taxon 9606], Escherichia coli (E. coli, species) [taxon 562]

## Full text

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## Figures

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## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12318758/full.md

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Source: https://tomesphere.com/paper/PMC12318758