Rare Neuroendocrine Tumor of the Bladder: A Case Report
Well-differentiated neuroendocrine tumors (WD-NETs) of the bladder are notably rare, representing only a small subset of neuroendocrine malignancies in this organ. We present a case of an asymptomatic 67-year-old Hispanic male in whom a WD-NET was incidentally identified during routine surveillance cystoscopy, six months following anterior urethroplasty with a buccal mucosal graft. The patient underwent two transurethral resections of the bladder tumor (TURBT). This case highlights the diagnostic challenges associated with WD-NETs given their rarity and reinforces the need for clinical awareness, even in patients without typical risk factors or symptoms.
Authors
- Omar Soto-Avilés (ORCID: https://orcid.org/0000-0001-8835-9971)
- Manuel Pizarro-Mondesir
- Laritza Fernandez-Claro
- Francisco Baralt-Nazario
Institutions
- University of Puerto Rico, Medical Sciences Campus (PR)
- Central University of the Caribbean (PR)
- Bayamón Central University (PR)
- University of Puerto Rico at Bayamón (PR)
Publication Details
- Journal
- Cureus
- Published
- 2025-09-12
- DOI
- https://doi.org/10.7759/cureus.92132
- Primary Topic
- Neuroendocrine Tumor Research Advances
- Type
- article
- Field-Weighted Citation Impact
- 0.00