# Urothelial Carcinoma of the Bladder with a Single Pancreatic Metastasis: A Case Report

**Authors:** Benedetto Calabrese, Nicola Frego, Vittorio Fasulo, Mauro Sollai Pinna, Gianluigi Taverna

PMC · DOI: 10.3390/reports9010081 · Reports - Clinical Practice and Surgical Cases · 2026-03-10

## TL;DR

A rare case of bladder cancer spreading to the pancreas is reported, highlighting the importance of accurate diagnosis for effective treatment.

## Contribution

The novelty lies in documenting a rare pancreatic metastasis from urothelial bladder cancer and emphasizing diagnostic approaches.

## Key findings

- Bladder urothelial carcinoma metastasized to the pancreas in a 65-year-old patient.
- EUS-guided biopsy with immunohistochemistry confirmed metastasis and excluded primary pancreatic cancer.
- The case underscores the need for precise diagnosis to guide therapies like immunotherapy and antibody–drug conjugates.

## Abstract

Background and Clinical Significance: Bladder cancer is common, with urothelial carcinoma (UC) comprising most cases in Western countries. Metastases usually involve pelvic structures, lymph nodes, and organs such as the liver, lungs, bones, and adrenal glands. Identifying unusual metastatic sites is critical for accurate diagnosis and treatment planning. Case Presentation: A 65-year-old man with a history of high-grade (G3) UC and carcinoma in situ, previously treated with TURBT, second-look resection, and SWOG-protocol BCG, presented with a new bladder lesion (pT1). Staging CT revealed extravesical spread and a 1.5 cm pancreatic body nodule. EUS-guided biopsy confirmed metastatic UC with concordant immunohistochemistry (GATA3+), excluding primary pancreatic cancer. The patient was referred for systemic therapy with immune checkpoint inhibitors and Enfortumab Vedotin. Conclusions: This case demonstrates the rare occurrence of pancreatic metastasis from bladder UC. EUS-guided biopsy with immunohistochemistry is essential to distinguish secondary lesions from primary pancreatic tumors. Accurate diagnosis is crucial to guide systemic therapy, particularly with emerging immunotherapy and antibody–drug conjugates.

## Linked entities

- **Proteins:** GATA3 (GATA binding protein 3)
- **Diseases:** urothelial carcinoma (MONDO:0040679), bladder cancer (MONDO:0004986), carcinoma in situ (MONDO:0004647)

## Full-text entities

- **Genes:** NECTIN4 (nectin cell adhesion molecule 4) [NCBI Gene 81607] {aka EDSS1, LNIR, PRR4, PVRL4, nectin-4}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, CDX2 (caudal type homeobox 2) [NCBI Gene 1045] {aka CDX-3, CDX2/AS, CDX3}, FGFR3 (fibroblast growth factor receptor 3) [NCBI Gene 2261] {aka ACH, CD333, CEK2, HSFGFR3EX, JTK4}, GATA3 (GATA binding protein 3) [NCBI Gene 2625] {aka HDR, HDRS}
- **Diseases:** urothelial involvement (MESH:D014526), Pancreatic Metastasis (MESH:D009362), CIS (MESH:D002278), injury to (MESH:D014947), pancreatic lesion (MESH:D010182), pancreatic cancer (MESH:D010190), non-papillary urothelial carcinoma (MESH:D002291), biliary obstruction (MESH:D001658), Bladder cancer (MESH:D001749), cytotoxicity (MESH:D064420), UC (MESH:D014523), pancreatic cysts (MESH:D010181), pain (MESH:D010146), pancreatic mass (MESH:D010195), LumP tumors (MESH:D009369), cystic (MESH:D018297), squamous-cell carcinoma (MESH:D002294), urothelial cell bladder carcinoma (MESH:D002292), lymphadenopathy (MESH:D008206), bladder lesion (MESH:D001745)
- **Chemicals:** Paclitaxel (MESH:D017239), MVAC (MESH:C044361), EV-302 (-), EV (MESH:C000632577), Taxotere (MESH:D000077143), platinum (MESH:D010984), Pembrolizumab (MESH:C582435), Gemzar (MESH:D000093542)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13030214/full.md

## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC13030214/full.md

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Source: https://tomesphere.com/paper/PMC13030214